Professional Documents
Culture Documents
Griffi
fiths, PhD, FRCR
Professor of Radiology and Head of Department, Academic Unit of Radiology,
University of Sheffield,
fi Sheffi
field, United Kingdom
Jeanne-Claudie Larroche
Ex-Directeur de Recherches au CNRS, Hôpital Port-Royal, Paris, France
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It became obvious in the late 1990s that magnetic reso- MR. I managed to contact Professor Larroche and was
nance (MR) imaging of the fetal central nervous system very pleased when she agreed to co-author this
was going to be more than an intellectual curiosity updated work with the Sheffield fi group. It has been a
wrapped around a technical challenge. There was (and great privilege to work with her.
remains in some circles) some resistance to accept that On a personal level, I have to mention my wife Jane,
there is any need for supplementing ultrasonography who is my inspiration, and on occasion, my refuge. Pro-
with fetal MR in cases of suspected developmental brain fessionally, I would like to acknowledge a number of
abnormalities. Many recent studies have shown value of people who have influenced
fl me over the years. Some
in utero MR of the fetus and there is also gathering inter- have shaped my thinking by reading their papers, hear-
est in postmortem MR of the fetus as an adjunct or ing them lecture, and subsequently coming to think of
replacement to autopsy. The problem was how to start. them as colleagues and I would include Jim Barkovich,
Few radiologists have experience of the normal MR app- Tom Naidich, Susan Blaser, and Erin Simon in that
earances of the brain at 20 to 40 weeks gestational age. group. More fundamentally, however, I need to acknowl-
Those who do have the experience have usually gained it edge the great burden of gratitude I owe to two people
from imaging premature babies in whom the predomi- who shaped my career at different stages. First, Profes-
nant pathologies are the complications of prematurity, sor Ian Isherwood, Professor of Radiology at the Univer-
not malformations. It has taken us a long time to build up sity of Manchester, who persuaded me to become a
a base of normal fetal brain examinations; therefore our neuroradiologist sometime in 1987, having known very
appreciation of age-related normality was slow to form. little about the speciality previously. And then there was
We hope, therefore, that this atlas will help others in this the late Derek Harwood-Nash! It was during my period
complex area of image interpretation. We must accept at the Hospital for Sick Children, Toronto, as the Neuro-
that fetal MR (particularly in utero MR) is still in its early radiology scholar in 1994-95 that Derek convinced me
stages of development. It is likely that in a few years I will that pediatric neuroradiology was the only game in
look back in horror at the quality of the images that we town, a decision I have not regretted since!
were expected to interpret, very much like modern feto-
Paul D. Griffiths
fi
maternal experts reviewing early obstetric ultrasonogra-
phy. But you have to start somewhere.
When people listen to you don’t you know it means a lot?
When I was struggling to come to terms with mid-
‘Cause you’ve got to work so hard for everything you’ve got
trimester brain anatomy I was fortunate to be directed
Can’t rest on your laurels now not when you’ve got none
to the pathology atlas of Alison Fess-Higgins and Jeanne-
You’ll find
fi yourself in a gutter right back where you
Claudie Larroche. The book was out of print and proved
came from.
difficult
fi to find but once it was located it was invaluable.
It occurred to me first of all that the book should be rep-
Novelty (I. Curtis)
rinted, but then considered an updated work including
iii
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SECTION TITLE v
contents
INTRODUCTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
INDEX 261
v
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INTRODUCTION
The development of the brain is an exceptionally com- brain abnormalities is diffi ficult with ultrasound; agen-
plicated process, which makes interpretation of radio- esis of the corpus callosum is a leading example.
logic images of the fetal brain challenging. Imaging of These factors have led many groups to explore alter-
the immature brain has become important in recent native methods of fetal and neonatal neuroimaging,
years for several reasons, with a corresponding in- most of which involve MR imaging. Another use for
creased requirement for clinicians with experience in MR imaging of the immature brain that has been ex-
fetal and neonatal brain imaging. One reason for this plored by a small number of groups, including our
need is the desire to detect abnormalities of the brain own, is postmortem MR imaging as either an adjunct
during the second trimester of pregnancy in order to or an alternative to autopsy. The drive for this in the
provide the best-quality information to parents about United Kingdom is the reduction in uptake of fetal/
the likely clinical sequelae of the anomaly. Second is the neonatal autopsy by parents concerned about the
need to investigate the increasing number of neonates well-publicized retention of tissues and organs with-
surviving premature delivery who are at high risk out consent at some British hospitals. It is possible to
for intracranial complications, both hemorrhagic and gain valuable information about brain abnormalities
hypoxic/ischemic. The need for imaging and the manner in the post 16-week fetus using postmortem MR imag-
in which it is delivered has infl fluenced the techniques ing and to inform parents about the risk to future
used. One of the overriding requirements is to not ex- pregnancies based on the anatomic definitionfi of the
pose the fetus or child to ionizing radiation or at least to malformation.
keep the exposure to the barest minimum because the The requirements for MR imaging of the brain in
potential risks are high in this population. A screening these three situations (in utero, postmortem, and post-
program of second-trimester fetuses cannot be built natal) are fundamentally different, but all have been
around an X-ray–based technique such as X-ray com- made possible by signifi ficant technologic advances in
puted tomography (CT), hence the rapid rise and refine- fi the field. They are also linked by another factor, namely,
ment of antenatal ultrasonography over the last few problems in interpretation for the reporter. A clinician
decades. It is also desirable to limit the amount of who reports imaging studies from any specialty has two
X-rays to which newborn babies are exposed, and ultra- basic tenets for his/her work: knowledge of normality
sonography has an important role here as well, although and knowledge of pathology. The purpose of this book
other factors are at play. Some ultrasound machines are is to assist clinical personnel involved in providing an
relatively inexpensive and are portable, making them imaging service to learn and understand normal MR
ideal for use in neonatal intensive care units given the appearances of the brain from the second half of preg-
risk management issues associated with moving a child nancy to 18 months postnatally.
from the neonatal intensive care unit to the radiology The histologic basis of this book is the Development
department. of the Human Foetal Brain: An Anatomical Atlas by
Recent studies have shown the limitations of ultra- Feess-Higgins and Larroche,1 which was published in
sound for assessment of the fetal and neonatal brain the 1980s but has been out of print for some time. It
that make the diagnosis of some types of pathology has been a great privilege for us to work with Professor
difficult
fi or impossible. For example, the early stages Larroche on this project. We have used a large number
of neonatal hypoxic/ischemic brain injury are difficultfi of the line diagrams and histologic photographs from
to show with transfontanelle ultrasonography; they the original INSERM publication in the production of
are shown much better by X-ray CT or magnetic reso- this atlas. The text of the original publication was in
nance (MR) imaging, particularly using diffusion- French and in English. The annotation of the line dia-
weighted imaging. It is becoming increasingly appar- grams was in Latin, as was the classic approach. We
ent that in utero detection of some developmental have decided to use a more anglicized approach to the
1
2 ATL A S OF FE T A L A ND POS T NA T A L BR A IN M R
The fundamental goal of this type of imaging is to more lipid is present in myelinated white matter than
obtain images with the highest anatomic resolution pos- in gray matter (54.9% dry weight vs 32.7%7). These two
sible (defifined as the smallest objects that can be resolved factors account for the superb gray/white distinction on
as separate). The two key elements in providing ana- T1-weighted MR imaging, particularly on T1 in the fully
tomic resolution are spatial resolution and contrast myelinated brain. The major difference in the brains of
resolution. Spatial resolution in imaging is dependent fetuses compared to adult brains is the virtual absence of
on the field of view and matrix size if the amount of MR myelin. In this case, the water content and the lipid con-
signal is not otherwise limited. Contrast resolution is tent of gray and “white” matter in the fetus are similar,
the ability to distinguish between two adjacent tissues of leading to the prediction of poor tissue contrast. This
different composition. In MR imaging this can be opti- certainly is the case for T1-weighted images where even
mized by knowing the composition of the tissue of inter- in the “ideal” imaging conditions of pmMR, obtaining a
est and modifying the MR sequences accordingly. In this T1 sequence with good tissue contrast for normal brain
respect, MR imaging and X-ray CT have comparable in- structures at 1.5 T is difficult,
fi at least in our experience.
plane anatomic resolution, but the improved contrast Tissue contrast between the future gray matter and white
resolution of brain structures provided by MR imaging matter structures is present on T2-weighted sequences,
makes it the method of choice in most circumstances. but the contrast is modest. However, some structures
The choice of sequence parameters is important present in the fetal brain, such as neuronal and glial peri-
for pmMR imaging. Over the 8 years that we have ventricular formation areas (germinal matrix) and the
performed pmMR, we have concluded that the best “transient fetal zones” within the developing cerebral
anatomic information from unfixed fi brain comes from hemispheres as described, greatly improve the predicted
T2-weighted images. As described in detail in Section 2, tissue contrast resolution.
this is in contrast to other groups that studied fixed
fi fetal The examinations shown in this atlas were performed
brains. In that situation, T1-weighted images seem opti- using either a 1.5-T or 3-T superconducting system
mal, at least in second-trimester fetuses. The precise (Infifinion 1.5T or Intera 3.0T, Philips Medical Systems,
optimal parameters we use for T2-weighted images Best, Netherlands). Brain imaging consisted of high-
required lengthy empirical experimentation (i.e., inspired resolution imaging in the three orthogonal planes using
guesswork!) in earlier pilot studies, but there were fast spin echo methods to produce T2-weighted images
theoretical and observational reasons to believe that using either a wrist or a knee coil (depending on the size
T2-weighted images would be superior. This is in com- of the fetus). The sequences at 1.5 T consisted of fast
parison with imaging of the adult brain, in which gray spin echo (echo train length 32) T2-weighted images
matter and white matter are best resolved on T1-weighted (TR 15,662 ms, TE 92 ms) with a bandwidth of 20.8 kHz
images. This can be explained by knowledge of the chem- using two acquisitions. A field
fi of view of 14 cm and ma-
ical differences between the brains of fetuses and adults/ trix size of 256 ⫻ 256 were used, giving in-plane resolu-
older children. MR images rely on hydrogen nuclei, and tion of 0.5-mm and 2-mm thick slices (no interslice gap)
the most abundant forms in the body are water and lip- of the whole brain. These parameters have now been
ids. There is approximately 82% water in mature gray used extensively to show both developmental and ac-
matter and 72% water in myelinated white matter,6 and quired fetal brain pathology postmortem (Figure 1).
A B
Figure 1 Postmortem magnetic resonance imaging at 1.5 T from two different cases. A, Image of an early second-trimester fetus with
alobar holoprosencephaly. B, Sagittal image of an early third-trimester fetus with a low occipital encephalocoele extending into the upper
cervical region.
4 ATL A S OF FE T A L A ND POS T NA T A L BR A IN M R
The cases included in this atlas acquired after 2006 of iuMR imaging over ultrasonography for developmental
were taken on a 3-T system. In theory, imaging at higher fetal neuropathology.9,10 One of the problems we faced
field strength should improve both anatomic and tissue
fi was lack of knowledge of normal second-trimester fetal
resolution of the fetal brain and allow better delineation anatomy as demonstrated by MR imaging. This problem
of the complicated infrastructure of the developing brain. continued for a considerable time because our examina-
Anecdotally this appears to be correct, but formal com- tions for the first
fi 4 years were performed as research stud-
parison is pending. The sequence data at 3 T are fast spin ies. We did not have approval from our local research
echo T2-weighted, echo train length 10, TR 4000 ms, TE ethics committee to study women with normal pregnan-
200 ms, flip angle 90°, field of view 120 mm, with recon- cies because of the unknown effects of iuMR imaging on
structed matrix size 640 ⫻ 640. Thirty 2-mm-thick slices the fetus, so we investigated only those fetuses with
with no gap and two excitations take 16 minutes to ac- known or suspected abnormality on ultrasonography.
quire. The resulting images produce excellent delinea- This is still the case now, although we offered fetomater-
tion of normal and abnormal fetal brain anatomy, but nal and genetic centers an iuMR facility (with the support
we also obtained some early good results producing of our local research ethics committee) to study women
T1-weighted images at 3 T (Figure 2). whose fetus was at higher risk from brain and/or spine
malformation. Many of those fetuses were normal, and by
obtaining clinical follow-up of those children, we built up
In Utero MR Imaging of the Fetus
a library of normal cases, some of which are used to
Our group has performed iuMR studies of the fetal illustrate this book.
brain since 1999 when clinical MR scanners with suffi- fi Full written consent is obtained from the woman by
cient gradient power to perform ultrafast imaging were the attending radiologist after explanation of the proce-
being produced. Fetal MR imaging had been performed dure. She is screened for the known contraindications
before that time, but mechanisms for preventing the to MR, as is her partner or relative if he/she intends to
fetus from moving were needed. Some groups used go into the MR scanner room with the mother. A fl flexible
muscular blockade of the fetus with pancuronium ad- phased-array coil is placed around the lower abdomen,
ministration into the umbilical vessels, usually while the and a series of three plane scout views is made to locate
vessel was being cannulated for another reason. Good the fetal brain. Fetal imaging is first fi performed in
images were obtained using standard sequences, but the an attempt to image the brain in the three natural
procedure was highly invasive and was associated with orthogonal planes using single-shot fast spin echo
risk to the fetus. A less invasive approach used intrave- (SSFSE) sequences initially with 5-mm-thick sections.
nous benzodiazepines to sedate the fetus, but monitor- The sequence parameters are TR 20,000 ms, TE 93.6 ms,
ing the mother in the MR environment presented other field of view 250 mm, matrix size 232 ⫻ 256, echo train
problems. The introduction of ultrafast MR imaging length 128, and flip angle 90°. The studies then are
methods into clinical practice has made iuMR imaging repeated using 3-mm-thick sections with parameters
(potentially) widely accessible. TR 21,032 ms, TE 103.6 ms, field of view 250 mm,
Our approach to iuMR imaging has been published matrix size 256 ⫻ 256, echo train length 140, and flip fl
previously,8 as have our results showing many advantages angle 90°. The acquisition times typically are 20 and
A B
Figure 2 Axial images at 3.0 T from postmortem magnetic resonance examination of a fetus with ventriculomegaly and hypoplasia of the
corpus callosum (confi firmed on sagittal imaging). A, Routine T2-weighted image. B, Equivalent T1-weighted image. Note the high-signal germi-
nal matrix and cortical plate on the T1 image. This contrast is a great improvement over the 1.5-T imaging we performed earlier. Note that the
region superfificial to the left germinal matrix shows postmortem damage and artifactual signal disturbance.
I N T R O D U C TIO N 5
25 seconds, respectively. These sequences provide heav- standard in this book and attempt to match the MR
ily T2-weighted images. As part of our imaging protocol, images to the tissue sections. This is relatively easy
we also acquire T1-weighted images in at least one with pmMR imaging because scan time is not an issue
plane (usually axial). The sequence we currently use is and there are no problems with movement. In con-
T1 RFFAST with parameters TR 210 ms, TE 4.47 ms, trast, this is a major problem for iuMR because of the
flip angle 80°, bandwidth 41.67 kHz, field of view
fl small moving target and the limited amount of time
250 mm, and matrix size 256 ⫻ 140. Twenty 5-mm-thick we believe a pregnant woman should be kept on the
sections take 29 seconds to acquire. MR scanner.
The major problem with T1-weighted iuMR images There are, however, more fundamental differences
of the fetal brain is the lack of inherent tissue contrast between the methods. The fetal tissue sections used in
because of high water and low lipid content. This com- the study came from brains that had been removed from
bination produces a very “flat”
fl image that, in our experi- the calvarium and fixed prior to staining. This has cer-
ence, has poor delineation even of the normal high sig- tain obvious and inevitable consequences. First, a large
nal from the germinal matrices on T1-weighted images. proportion of the extraaxial anatomy is lost, unlike the
Therefore we use this sequence to look for abnormal in situ pmMR cases shown in this atlas and the iuMR
fat-containing structures or subacute hemorrhage. No cases. Second, the fixation process itself likely has some
T1-weighted fetal images are shown in this atlas. effect on the overall morphology of the brain as the al-
Although the individual acquisitions are only in the or- teration of protein elements and the removal of water
der of 20 to 30 seconds, the table occupancy time can be likely have differential effects on different parts of the
quite long because of fetal movement and the “chasing” brain. For example, in our experience (and that of other
required to obtain the orthogonal planes. Experienced workers), the cortical sulci appear more prominent on
radiographers are vital to reduce the overall examina- tissue sections than on pmMR images when fetuses of
tion time; in most cases we can obtain all of the se- the same gestational age are matched. It also is likely
quences described in less than 20 minutes. that the relative effacement of cortical sulci seen on
pmMR imaging compared to the other techniques re-
sults from premortem swelling of the brain prior to
Postnatal MR Imaging
abortion.
The five cases used to illustrate the postnatal section One of the major advantages of histologic studies of
are taken from children who were being investigated the brain is the ability to use different staining meth-
for possible head injuries but who had no focal neuro- ods to show different cellular elements to advantage.
logic problems, had normal X-ray CT and MR exami- The two categories of stains used in the Larroche atlas
nations, and were normal at clinical follow-up. All of were “histologic” (hematoxylin–eosin or cresyl violet)
the children were examined under general anesthesia and myelin stains (Loyez or Luxol fast blue). Although
using the following parameters: (1) Fast spin echo we can use different sequences and parameters in
T2-weighted, echo train length 8, TR 4500 ms, TE 94.5 pmMR imaging, we cannot hope to rival the tissue
ms, field of view 240 mm, matrix size 352 ⫻ 512, two contrast provided by histologic stains. In some cases
excitations. Sections 5 mm thick were taken with a this is of little detriment; for example, the germinal
1-mm gap, and 21 slices took 6 minutes 36 seconds to matrix has a signifi ficantly lower signal on T2-weighted
acquire. (2) Spin echo T1-weighted, TR 588 ms, TE images and is well demonstrated on both pmMR im-
15.2 ms, field of view 240 mm, matrix size 256 ⫻ 256, ages and stained tissue sections. On the other hand,
two excitations. Sections 5 mm thick were taken with the transient layers within the fetal white matter are
a 1-mm gap, and 21 slices took 5 minutes 2 seconds to present but are more difficult
fi to separate on pmMR
acquire. images than on histologic sections. It should also be
remembered that MR sections are much thicker than
histologic sections.
Differences Between the Techniques
Many other features seen in postmortem fetal brains
The three imaging methods used to illustrate fetal result either from the effects of the fetal demise itself or
brain anatomy in this atlas are not directly compara- as a complication of traumatic delivery. Some damage
ble for many reasons. The fi first and most obvious to normal brain anatomy is commonly seen on post-
problem is that the iuMR, pmMR, and histologic mortem studies (both autopsy and pmMR), and some
sections were obtained from different individuals. structures (e.g., fetal corpus callosum) show marked
Suffificient variation among individual fetal brains en- susceptibility to artifactual injury. This was discussed
sures that perfect matches can never be made. An in Larroche’s atlas and is seen on pmMR, such as the
added complication arises when trying to ensure the 19- to 20-week case used to illustrate this book. MR
sections have been taken from matched anatomic imaging is highly sensitive to early subacute hemor-
planes. This is a particular problem for axial and rhage, and intraventricular, germinal matrix, and/or
coronal images where the planes of section are arbi- choroid plexus hemorrhage are commonly seen on
trary, unlike sagittal/parasagittal images where the postmortem MR. We believe that, in many cases, this is
plane of section is easily defined.
fi We use the tissue an effect of the fetal loss per se and is not the cause of
sections in the original Larroche atlas as the reference the abortion.
6 ATL A S OF FE T A L A ND POS T NA T A L BR A IN M R
The adult human brain has a highly complex external one issue, and the mechanisms for estimating the dates
morphology, and this is particularly true of the cerebral of a pregnancy have wide margins of error. In addition,
hemispheres. The clinical neuroimager needs to know the possible signifi
ficant differences in the degree of sul-
the normal patterns of cortical gyri and their associated cation between the two hemispheres within the same
sulci in order to make accurate anatomic diagnoses that individual are well documented.
will assist in functional assessment and/or surgical plan- The purpose of this section is to show the development
ning. Someone looking at the surface of the adult brain of the surface cortical patterns of the fetal brain between
for the fi
first time likely would be convinced by the appar- 19 weeks’ gestational age and term. We recommend that
ent randomness of the convoluted surface. However, it you refer back to this section when studying the cross-
becomes apparent that the gyri/sulci form patterns that sectional images of the appropriate gestational age in
are common among individuals and, although variations Section 2 or the neonatal cases in Section 3 because an
exist, a large number of recurring themes can be found. understanding of sulcation both on cross-sectional imag-
It is important for anyone trying to understand the devel- ing and on representations of surfaces is necessary. This
opment of fetal cerebral hemispheres for diagnostic section begins with a discussion of the appearances of the
purposes to have a deep understanding of the finalfi adult major cortical sulci that may be described as mature” or
patterns and common variations. It is also necessary to adult pattern. This section uses the surface projections of
appreciate the gestalt of being able to understand the the developing fetal brain from the Larroche atlas.3
surface anatomy of the brain and applying that knowl-
edge when interpreting cross-sectional imaging studies.
Naidich et al.1,2 have provided many illuminating publi-
ANATOMY OF THE SULCI AND FISSURES
cations on the subject, and the interested reader is IN THE “MATURE” SUPRATENTORIAL
directed to their work. BRAIN
Before 16 weeks’ gestational age the fetal human ce-
rebral hemispheres are effectively smooth and feature- The cerebral hemispheres are separated from each
less. In contrast, the overall degree of sulcation at birth other in the midline by the median (great) longitudinal
is effectively the same as the adult pattern. The huge fissure and its contents: the pia and arachnoid mater
fi
changes in the external morphology of the brain that with the intervening subarachnoid space that overlie
occur between those two time points are due to the de- both cerebral hemispheres, and two layers of dura ma-
velopment of the cerebral cortex and the massive num- ter that are fused for the most part as the falx cerebri.
bers of neurons and glia that migrate there from the The inferior sagittal sinus is contained within the free
germinal matrices. The gyral convolutions produce a inferior border of the falx, whereas superiorly the two
greater surface area per unit volume compared with the leaves of dura separate to contain the superior sagittal
smooth, agyric cortex present in many other mammals. sinus (Figure 1-1). The falx is attached to the crista galli
Indeed, the gyric human cerebral cortex is estimated to anteriorly, where it is quite narrow, but it widens as it
have three times the surface area as an agyric brain of sweeps posteriorly and eventually attaches along the
the same volume. The major sulci of the brain tend to midline of the tentorium cerebelli. The drainage of ve-
appear in an ordered and predictable sequence, and the nous blood in the sagittal sinuses normally is from an-
person interpreting fetal magnetic resonance (MR) terior to posterior; therefore the structure increases in
images should be aware of the normal patterns and size passing posteriorly to accommodate for increasing
schedules of appearance. However, the patterns are only drainage from the cortical veins. These features are well
approximations, and one should not expect to be able to shown on coronal MR imaging.
defifine with any degree of accuracy the gestational age of The surfaces of the cerebral hemispheres show many
a fetus based on the sulcal patterns. Biologic variation is convolutions consisting of cortical gyri separated by
7
8 ATL A S OF FE T A L A ND POS T NA T A L BR A IN M R
Arachnoid
Venous Superior granulations
lacuna sagittal sinus
Venous
Emissary lacuna Dura matter
vein
Diploic
vein
Superior Superior
sagittal frontal
Falx sinus gyrus
cerebri
Cingulate
sulcus
Callosal
Inferior Cingulate sulcus
Branches sagittal gyrus
of the sinus
anterior
cerebral Corpus
artery callosum
B C
Figure 1-1 Anatomy of the median longitudinal fi fissure. A, Line diagram of the anatomy of the medial longitudinal fi fissure and its contents
in the coronal plane. (From Stranding S [ed]: Gray’s Anatomy, 39th ed. Edinburgh, Elsevier, 2005.) B, C, Coronal T2-weighted images from a
3-year-old child with mild atrophic changes due to an unknown, progressive degenerative process of the brain. Showing respectively the
contents of the median longitudinal fissure and the adjacent brain anatomy. The midline falx cerebri has low signal on this sequence
because of its high fibrous content. The superior and inferior sinuses related to either end of the falx have low signal because of flow
phenomena (as for the branches of the anterior cerebral artery). Free water has high signal on this sequence, which explains the high signal
in the cortical sulci and other cerebrospinal fluid–containing spaces.
SU R F A C E A N A T O M Y O F T H E BR A IN 9
sulci of varying sizes. Most of the sulci are prominent descending rami.4 Naidich et al. have shown that the
and easily delineated in whole brain preparations, and anatomy of the subcentral gyrus is well seen on MR, and
many of them are constant between individuals. The this topic is discussed in the section on locating the cen-
cerebral cortex and associated white matter form four tral sulcus.
lobes in each hemisphere (frontal, temporal, parietal, The insula is defi fined as the cortical surface in the
occipital), and those lobes are (incompletely) defifined by depth of the lateral fissure
fi and is considered to be the
prominent, relatively constant sulci. The appearances “fifth
fi cortical lobe” by some researchers. The mature
of sulci on imaging studies can be appreciated only if insula has a complicated surface structure, which is
the anatomy of the meninges is understood. The inner- best appreciated on whole brain preparations when the
most layer of the meninges, the pia mater, is closely opercula have been removed (similar “virtual” proce-
adherent to the surface of the brain at all sites. In con- dures can be performed on T1-weighted volume data;
trast, the thicker arachnoid mater encompasses the Figure 1-4). The insula is pyramidal in shape, with its
brain without extending into the recesses. The sub- apex directed inferiorly and anteriorly. The apex is the
arachnoid space lies between the two, contains cerebro- only portion of the insula that is not bounded by the
spinal fluid (CSF), and usually is quite thin. However, circular gyrus. The large central insular sulcus runs
some regions contain local dilatations of the subarach- from the apex, superiorly and posteriorly to form larger
noid space with large pools of CSF. One such region is anterior and smaller posterior surfaces. The posterior
the basal cisterns related to the inferior surface of the region usually is divided by a single sulcus to form two
brain; another is the space between adjacent cortical “gyri longi,” whereas the anterior area is inconsistently
gyri. Thus the cortical sulci have the same intensity as divided into three or four “gyri brevi.”
the fluid within the ventricles on all sequences (e.g.,
high signal on T2-weighted images), and their shape is
Central Sulcus
dependent solely on the shape of the adjacent gyri. The
major sulci and associated brain structures of a fetus of This prominent sulcus on the lateral aspect of the cere-
40 weeks gestational age are shown in Figure 1-2. bral hemisphere barely extends onto the medial surface,
if at all. The central sulcus separates the frontal and
parietal lobes, and the frontal lobe can be completely
MAJORR SULCI RESPONSIBLE delineated by the lateral and central sulci on the lateral
R DEFINING LOBAR
FOR R ANATOMY surface of the brain. It takes a curved course posteriorly
at approximately 70° towards the lateral sulcus but does
These consist of the lateral (sylvian) sulcus, central sul- not contact it. The postcentral sulcus lies approximately
cus, and parieto-occipital sulcus. For the most part the 1.5 cm posterior to the central sulcus and runs parallel
lobar anatomy is best defined
fi on the lateral surface of to it. The correct localization of the central sulcus is
the brain by the lateral and central sulci. hugely important on cross-sectional imaging as it de-
fines the primary motor cortex anteriorly and the pri-
mary sensorimotor cortex posteriorly. This can be diffi- fi
Lateral Sulcus
cult and is best achieved on axial imaging as described
The lateral sulcus is a deep fi
fissure that is first identifi
fied in the section on the cingulate sulcus.
on the inferior surface of the brain close to the anterior
perforated substance but becomes most visible on the
Parieto-occipital Sulcus
lateral surface where it separates the frontal and pari-
etal lobes from the temporal lobe. The frontal lobe is This is predominantly a feature of the posterior por-
separated completely from the temporal lobe, whereas tion of the medial hemispheric surface, although it
the posterior aspects of the parietal and temporal lobes can extend onto the lateral surface for a short way in
remain in continuity without a well-defined fi external some cases. It runs inferiorly and slightly anteriorly,
border. The parts of the frontal, temporal, and parietal separating the precuneus of the parietal lobe and the
lobes that protrude into and surround the lateral fissure
fi cuneus of the occipital lobe before joining the calca-
are called the opercula. The anatomy of the lateral sul- rine fi
fissure.
cus on the lateral surface of the brain is complicated as Note that a temporo-occipital sulcus exists on the
it divides into three rami: anterior horizontal, anterior inferior surface of the brain but has highly variable
ascending, and posterior. These can be seen well on MR appearances.
imaging that allows nonorthogonal plane reformation
of volume data (Figure 1-3). The anterior horizontal ra-
mus protrudes into the inferior frontal gyrus running OTHERR SULCI OF IMPORTANCE
horizontally and anteriorly. The anterior ascending ra-
R FETAL IMAGING
FOR
mus runs vertically into the same gyrus and definesfi the
pars triangularis portion of the inferior frontal gyrus
Superior and Inferior Frontal Sulci
anterior to the ascending ramus and the pars opercu-
laris posteriorly. The posterior ramus extends posteri- The lateral surface of the frontal lobe is indented by
orly and slightly superiorly for approximately 8 cm be- two sulci running in a broadly horizontal fashion, the
fore dividing into the posterior ascending and posterior superior and inferior frontal sulci. These demarcate
10 ATL A S OF FE T A L A ND POS T NA T A L BR A IN M R
Precentral gyrus
Central sulcus
Postcentral gyrus
A Parieto-occipital
P i i i l sulcus
l
Supramarginal gyrus
Superior frontal sulcus
Pa
arieto-occipital sulcus
Occipital lobe
La
ateral sulcus
Superior temporal gyrus
S
Superior
temporal
sulcus Inferior
temporal Inferior temporal gyrus
Middle
sulcus
temporal gyrus
B
Figure 1-2 Surface features of a 40-week gestational age fetus. A, Superior. B, Lateral.
SU R F A C E A N A T O M Y O F T H E BR A IN 11
Olfactory trac
ct
Optic chiasm
Pons
Inferior temporal gyrus
Medulla
Cerebellar hemisphere
Central sulcus
Callosal sulcus
Cing late gyrus
Cingulate g r s Pars marginalis of cingulate
c sulcus
Supe
erior frontal gyrus
Cingula
ate sulcus Precuneuss
Pa
arieto-occipital sulcus
Corpus callosum
m
Cuneus
Calcarine sulcus
Optic chiasm
Pons
Cerebellar verm
mis
Medulla
D
Figure 1-2, cont’d C, Inferior. D, Medial. The same annotation is used for these figures as in the developmental series at the end of the section.
12 ATL A S OF FE T A L A ND POS T NA T A L BR A IN M R
6
1
Anterior Central
ascending ramus sulcus
Posterior
ascending
ramus
Anterior
horizontal
ramus
Posterior
descending
ramus
Stem of
lateral
sulcus
Posterior
horizontal
ramus
B
Figure 1-3 Anatomy of the lateral sulcus and surrounding brain on magnetic resonance imaging. The anatomy of the lateral sulcus can be
studied on parasagittal sections of the brain but often is best shown using nonorthogonal curvilinear reformations of T1-weighted volume
data. A, Plane of reformation on axial section (same case as Figure 1-1). B, C Same curvilinear reformation showing the sulci and brain
structures, respectively. Note the pars orbitalis, pas triangularis, and pars opercularis all are subdivisions of the inferior frontal gyrus.
SU R F A C E A N A T O M Y O F T H E BR A IN 13
Precentral
gyrus
Postcentral
gyrus
Pars
opercularis
Subcentral
gyrus
Pars
triangularis
Pars
orbitalis
Superior
temporal
gyrus
C
Figure 1-3, cont’d
Central
al
sulcus
s
Circular sulcus
C
Central
insular sulcus
Gyrus brevi
G b i Gyrus
G
A longus
Central
insular sulcus
Gyri
brevi
Gyri
longi
Lateral
sulcus
B
Figure 1-4 Anatomy of the insula. A, Line diagram depicting the anatomy of the insula. (From Stranding S [ed]: Gray’s Anatomy, 39th ed.
Edinburgh, Elsevier, 2005.) B, Sagittal oblique reformation of T1-weighted volume images from a child with no structural brain abnormality.
The insula is divided into a larger anterior part (containing the gyri brevi) and a smaller posterior part (containing the gyri longi) by the
central insular sulcus.
A B
Central sulcus
Precentral
gyrus
Postcentral
sulcus
Postcentral
gyrus
Pars
marginalis C D
Figure 1-5 Effects of scan angulation on the anatomy of the paracentral lobule on axial imaging. All images from a T1-weighted volume data
set of a 4-year-old child with no structural brain abnormality. A, Sagittal image just off midline showing the cingulate sulcus (arrow) and its pars
marginalis portion (arrowhead). B is the equivalent image showing the approximate angulation used for X-ray computed tomographic proce-
dures. C shows the normal anatomy of the paracentral lobule on “MR angulation” whilst D shows the equivalent “CT angulation”. The position
of the pars marginalis is shown for comparison in D.
merely an oblique indentation in the lateral aspect of brain in the axial plane allows good assessment of devel-
the second-trimester hemisphere. Over time it deepens oping opercularization. The anterior and posterior lips
and develops secondary sulci on the insular cortex, and of the opercula are everted up to 20 weeks’ gestational
the opercula portions of the surrounding frontal, pari- age, but rapid cortical/subcortical growth causes the lips
etal, and temporal lobes completely cover the insula, as to grow toward each other, a process that is quite ad-
described previously. The insular sulci form late. Garel vanced by 26 weeks’ gestational age. Garel assessed this
did not see any evidence of the insular sulci before development by measuring the distance between the
31 weeks, and those structures were present in only 10% anterior and posterior opercula and found few cases
of 31-week fetuses. Insular sulci were present in all where the interopercular distance was less than 10 mm
36-week gestational age fetuses. Imaging of the fetal before 29 weeks. The distance then gradually reduced so
SU R F A C E A N A T O M Y O F T H E BR A IN 17
that at 36 weeks’ gestation, for example, 80% of values of fetuses had defifinable superior temporal sulci by
were between 4 and 8 mm. However, the opercula did 31 weeks and inferior temporal sulci by 30 weeks.
not close completely before birth in any of the cases, so
this event appears to occur postnatally. Cortical malfor-
Calcarine Sulcus
mations may disrupt this process, but underopercular-
ization without obvious structural abnormality is one of This feature of the medial portion of the occipital lobe
the “soft” neuroradiologic features seen with high fre- is well-visualized on both coronal and sagittal images
quency in children with developmental delay. close to the midline. It is seen in two thirds of 22-
The central and precentral sulci are early features on to 23-week fetuses and in all fetuses after 25 weeks’
the lateral surface of the developing hemispheres, with gestation.
the central sulcus appearing fi first. Both structures are
best assessed on axial imaging of the fetal brain. Garel
Collateral Sulcus
found that the central sulcus was seen in 20% of her
cases at 22 to 23 weeks, in 75% of cases at 26 weeks, and The coronal plane is optimal for assessing this sulcus,
in all cases thereafter. Our experience is broadly compa- although ensuring that some of the rhinal sulcus is not
rable, although we saw the central sulcus consistently in included, particularly on 5-mm-thick sections, may be
25- to 26-week fetuses on iuMR imaging. In contrast, diffi
ficult. This sulcus is visualized in more than 50% of
the precentral sulcus was not shown by Garel before cases at 26 weeks and in all normal fetuses at 28 weeks
26 weeks but was seen in 90% of 28-week fetuses and and later.
consistently after that time. The parieto-occipital sulcus The overall results of fetal sulcation are summarized
is best appreciated on sagittal images of the fetus. in Table 1-1. Much more work is needed in this field in
It is visible after 22 weeks’ gestational age in the vast order to obtain more robust data. Garel’s textbook did
majority of, if not all, fetuses. not extend back before 22 weeks’ gestational age, and
the number of cases under 25 weeks is limited. This is
unfortunate because of the great need to understand
normality in second-trimester fetuses so that robust
OTHERR SULCI OF IMPORTANCE interpretation of abnormal cases can be made. A corol-
R FETAL IMAGING
FOR lary of this in clinical practice is the urgent need for
research on the gestational age at which neocortical
Superior and Inferior Frontal Sulci formation abnormalities can be confi fidently diagnosed
or excluded. For example, lissencephaly is an uncom-
Both of these sulci are best assessed on coronal images mon malformation of cortical development, and the
of the fetal brain. The data from Garel suggest the two imaging features of lissencephaly are well described.
sulci appear at approximately the same time, although Most cases show an absence or paucity of sulci with
fetuses with superior frontal sulci without inferior fron- wide, abnormal gyri, which produce smooth hemi-
tal gyri, but not vice versa, are a common finding. Both spheric surfaces. If the only diagnostic feature of lis-
sulci are seen in a minority of fetuses at 26 weeks but in sencephaly is lack of sulcation, how can the condition
a majority at 27 weeks. Both sulci are consistently seen be diagnosed in the fetus when the normally developing
at 30 weeks and after.
early brain is agyric? Although many cases of pediatric studies appear to be the only chance for early detection
lissencephaly do have abnormal thickening of the cere- of abnormalities such as lissencephaly. This may be an
bral cortex, this may not be obvious while the cortex is overoptimistic view, however, remembering that pa-
still developing in utero. The accuracy of in utero imag- thologists have said for many years that accurate
ing in diagnosing lissencephaly at different stages of assessment of gestational age by inspection of fetal
pregnancy is not known. In our experience, the vast brains (certainly within 2 weeks) is not possible. The
majority of cases are not diagnosed by antenatal ultra- following figures
fi show the normal changes in the sur-
sound in the second trimester, and it seems that iuMR face appearance of the fetal brain between 19 and
also misses many cases of the subtler abnormalities of 37 weeks gestational age. Please note that there has
cortical formation in the second trimester. Therefore been no attempt to scale the images with respect to the
performing further studies of normal sulcation in the different gestational ages for purposes of anatomical
second-trimester fetus is vital because, for now, such clarity.
19
20 ATL A S OF FE T A L A ND POS T NA T A L BR A IN M R
Prece
entral sulcus
Central sullcus
Pre
ecentral gyrus
Parieto-occipital sulcus
Pre
ecentral gyrus
Central sulcus
Postcentral gyrus
Postcentral sulcus
Superior frontal
f sulcus
Pre
ecentral sulcus
Precentral gyrus
P
Central sulcus
C
Postcentral gyrus
Postcentral sulcus
SUPERIOR SURFAC
CE, 32–33 WEEKS Parieto-occipital sulcus
Median longitudinal
fissure
Precenttral gyrus
Ce
entral sulcus
Posttcentral gyrus
SUPERIOR SURFAC
CE, 36–37 WEEKS Occipital lobe
LATERAL SURFACE
23
24 ATL A S OF FE T A L A ND POS T NA T A L BR A IN M R
Lateral sulcus
Cerebelllar hemisphere
Insula
Cerebe
ellar hemisphere
Central sulcus
Precentral gyrus
gy
Postcentral gyrus
Lateral sulcus
Insula
Central sulcus
Precentral gyrus Postcentral gyrus
Supramarg
ginal gyrus
Sup
perior temporal gyrus
Insula
Lateral sulcus
Precentral sulcus
Supramargiinal gyrus
Occipital lobe
O
Insula
Precentral
gyrus Central sulcus
Superior frontal gyrus
Postcentral gyrus
Postcentral sulcus
Middle frontal gyrus
Supramarginal gyrus
Precentral sulcus
erior
Infe
fronntal Occcipital lobe
gyyrus
Insula
Lateral
sulcus Middle tempo
oral gyrus
Superior
temporal Superior
gyrus temporal Inferior Inferior temporal gyru
us
sulcus temporal
LATERAL SURFACE, 36–37 WEEKS sulcus
INFERIOR SURFACE
27
28 ATL A S OF FE T A L A ND POS T NA T A L BR A IN M R
Olfactory tract
Late
eral sulcus
Lateral sulcus
Pons
Olfactorry tract
Lateral sulc
cus
Po
ons
Cerebellar hemisphere
C
Medulla
Olfactory tract
Lateral sulcus
Op
ptic chiasm
Pons
M
Medulla
Median
longitudinal Olfactory sulcus
fissure
Olfactory tra
act
Laterral sulcus
Optic chiasm
Pons
Cerebellar hemisphere
Medulla
INFERIOR SURFACE, 32
2–33 WEEKS
Median longitudinal fissure
Olfacctory tract
Optic chia
asm
Cereb
bellar hemisphere
31
32 ATL A S OF FE T A L A ND POS T NA T A L BR A IN M R
Callosal sulcus
Corpus callosum
Parieto-occipital sulcus
Calcarine su
ulcus
Fornix
Thalamus Midbrain
Callosal sulcus
pus callosum
Corp
Parieto-occipital sulcus
Calcarine
e sulcus
Pineal gland
Midbrain
MEDIAL SURFACE, 22––23 WEEKS
SU R F A C E A N A T O M Y O F T H E BR A IN 33
Callosal
sulcus
Cingulate sulcus
Cingulate gyrus
Parieto-occipital sulcus
Corpus callosum
Cuneus
Calcarine sulcus
Midbrain
Thalamus
Cerebellar vermis
Cingulate
sulcus Central sulcus
Callosal sulcus
pars marginalis of
cingulate sulcus
Cingulate gyrus
Precuneus
Corpus callo
osum
Parieto-occipital sulcus
Cuneus
Calcarine sulcus
Olfactory tract
Thalamus
Cerebellar vermis
Corpus
Superior frontal gyrus callosum Central sulcus
Cingulate gyrus
Cingulate sulcus
Callosal
sulcus
Precuneus
Parieto-occipital sulcus
Cuneus
Olfactory tract
Thalamus
Pons Midbrain
Cerebellar vermis
Cingulate
pars marginalis of
sulcus
Superior frontal gyrus cingulate sulcus
Callosal sulcus
Precuneus
Cingulate gyrus
Parieto-occipital sulcu
us
Corrpus
callossum
Cuneus
Calcarine sulcuss
Thalamus Optic
chiasm
Midbrain
Pons Cerebellar vermis
Medulla
MEDIAL SURFACE, 36–37 WEEKS
section 2
SECTIONAL ANATOMY
OF THE FETAL BRAIN
The major part of this section is a pictorial review of future cortex and deep gray matter structures. Recently,
cross-sectional fetal brain anatomy using magnetic res- there has been considerable interest and research in
onance (MR) imaging matched as closely as possible the development of the cerebral cortex in the human
with postmortem histologic sections. It should be ap- fetus. The second trimester is an exceptionally active
preciated that by the time the fetal brain has reached period of neuronal/glial cell birth, proliferation, and
19 to 20 weeks (the earliest fetal images shown in this migration. MR imaging has played a role because it
text), all of the major structural components visible in allows visualization of the normal structures of the
routine neuroradiologic practice have formed and are developing cerebral hemispheres, which appear to cor-
clearly visible. Because of this, previous knowledge of respond to the features shown on histologic studies.4
adult neuroanatomy can be used to a large extent; in- This has had important clinical repercussions for clas-
deed, the basic neuroanatomy does not change during sifying neocortical brain malformations on pediatric
this period. The diffi ficulty in interpreting fetal and neo- neuroimaging.5,6
natal imaging arises in the evolving anatomic features of One of the striking macroscopic and histologic fea-
the brain. We discussed the evolution of the “sulcated tures of the fetal brain is the presence of large germinal
brain” at the start of Section 1 and myelination is dis- matrices adjacent to the ventricles, which are particu-
cussed in Section 3, which covers postnatal imaging. larly prominent in the second-trimester fetus.7 The pri-
The purpose of this section is to give an introduction to mary germinal matrix or neuroepithelium is a cell-dense
the transient structures in the wall of the developing structure that lines the cerebral ventricles. Those cells
fetal brain, that is, structures that are not found in the proliferate extensively and produce neurons, glia, and
adult, pediatric, or even the term newborn brain. the secondary germinal matrix. Bayer and Altman7
found that the secondary germinal matrix (or subven-
tricular zone) produces mainly neurons that are des-
TRANSIENT STRUCTURES IN THE FETAL tined to become cortical interneurons and astrocytes.
CEREBRAL HEMISPHERES Some of the secondary germinal matrices migrate away
from the ventricles and complete their cell-producing
The original Larroche atlas used anatomic terminology role at sites distant from the ventricles. Leading among
from the Nomina Anatomica of the International Ana- these are the matrices that form the granule, basket and
tomical Nomenclature Committee.1 As explained in the stellate cells of the cerebellar cortex, and granule cells in
introduction of the Larroche atlas, some anatomic fea- the dentate gyrus of the hippocampus.
tures are not fully covered by Nomina Anatomica, par- At some sites in the brain of the second-trimester
ticularly structures peculiar to the developing brain. fetus the germinal matrix is particularly large and is
The authors made reference to more specifi fic papers, named by the structures that ultimately will be pro-
such as the work of Rakic and Yakovlev2 and Angevine duced. For example, large neuroepithelial/subventricular
et al.3 in order to assist with nomenclature. The two zones are found around the lateral ventricles and are
main structures that are found in the fetus but not in called the striatal matrices because they will form the
the brain of adults or children are the subependymal putamen and caudate. Feess-Higgins and Larroche used
germinative zones (“germinal matrix”) and the tran- terms such as matrix rhombencephalica, matrix mesence-
sient laminated structures found in the developing phalica, and matrix telencephalica in their atlas (but
cerebral hemispheres. The latter arise from the ventri- labeled simply as matrix in the fi figures of the original
cofugal migration of neurons and glia toward the text) to distinguish the anatomic site of the germinal
35
36 ATL A S OF FE T A L A ND POS T NA T A L BR A IN M R
matrix and therefore imply the structures formed from more, Kostovic et al showed that those glial structures
those regions of neural/glial proliferation. In this atlas guide the migration of cells formed in the germinal
we simply use the term germinal matrix in our annota- matrix to a predetermined site in the developing cortex
tion in the hope that which portion of the ventricular by a process called fate mapping. Those radial fibers
fi can-
system is adjacent is obvious. This simplification
fi does not be resolved on MR imaging, although their presence
not undervalue the importance of the germinal matrix can be inferred in some developmental abnormalities
from either a developmental or an imaging point of such as focal cortical dysplasias and cortical tubers
view. On the contrary, the germinal matrix is a promi- associated with tuberous sclerosis complex.11 The obser-
nent landmark on fetal MR imaging, particularly in the vations by Bayer and Altman stress, however, that the
second trimester, and may hold the key to early detec- intermediate zone should not be viewed as a passive
tion of some disorders of cortical formation. structure, merely allowing the transit of neurons and
The germinal matrix is one of the few structures in glia en passant. Instead it is an important region where
the normal fetal brain that has very short T2 values (i.e., cell migration is arrested to allow stratification
fi and
appears dark on T2-weighted images). This feature pro- early synaptic contact. The authors suggest that “precor-
vides superb contrast between the high signal of the tical” interactions are vital for normal cortical develop-
cerebrospinal fluid
fl in the ventricles on its deep surface ment. By implication the intermediate zone must be an
and the intermediate signal of the developing brain su- important area of further imaging research in cases
perfificially. This tissue contrast is exceptionally well seen where the neocortex does not form properly.
on postmortem MR (pmMR) because of the lack of time Bland and Altman describe six different regions in
constraints that allow the use of sequences with low the intermediate zone: stratified
fi transitional fields 1 to 6
echo train lengths and high number of excitations. The (i.e., STF1 [superfi ficial] through to STF6 [abutting the
contrast resolution of the germinal matrix is sometimes germinal matrix]). These strata develop in the fi first tri-
poor on in utero MR (iuMR) using single-shot fast spin mester but undergo considerable growth in the second
echo (SSFSE) sequences. This is partly due to the low trimester and for the most part have undergone involu-
sensitivity to susceptibility changes because of the blur- tion in the third trimester, although some portions per-
ring brought about as a result of the high number of sist to become the established mature white matter.
echoes in the sequence (T2 decay k-space filtering). The Histologically, significant
fi differences between the STF
primary and secondary germinal matrices can be shown strata in regions will become “sensory regions,” with
and differentiated on histologic studies. On MR imag- large numbers of granular cells in layer IV (granular
ing, however, the two structures cannot be resolved even cortex) in the mature brain, and the “motor regions”
on high-resolution pmMR because they are so closely with greater numbers of pyramidal cells in layer V
opposed and have identical signal characteristics. The (agranular cortex). In principle, knowledge of the strata
pmMR images in this atlas show the primary and and their contents can help explain the regional differ-
secondary matrices clearly on 19- to 20-week, 22- to ences in MR signal seen in the second-trimester fetal
23-week, and 25- to 26-week fetuses, and the matrices brain on pmMR and, to a lesser extent, on iuMR.
can often be seen on iuMR at these gestational ages. STF1 lies just below the cortical plate and is a rela-
However, by 29 to 30 weeks, the germinal matrices are tively thick structure. It contains mainly fibrous
fi struc-
less distinct on pmMR, and by 32 to 33 weeks they can tures with a large proportion of free extra-cellular fluid
fl
be seen only in a minority of sites. and few cell bodies. It has high signal on T2-weighted
The other transient structures that are of great inter- images in contrast to the low-signal cortical plate
est to researchers in the field are the laminar, cellular superficially.
fi It is seen in both granular and agranular
compartments within the developing cerebral wall cortices and will become the subcortical white matter.
that ultimately will govern the organized formation of STF2 and STF3 are cell-rich regions and are the last
the cortex and other subcortical gray matter regions “sojourn” site before neurons and glia enter the cortical
of the cerebral hemispheres. Bayer and Altman7 discuss plate. STF2 is most prominent in agranular cortex; STF3
the historical approach to describing the developing is found only in granular cortical regions. Both of these
cerebral mantle and explain the new developments in structures have disappeared in the mature brain. STF4,
understanding the process. The classic description of STF5, and STF6 are fibrous, cellular, and fibrous, respec-
the second-trimester cerebral cortex involves only three tively. STF5 is thought to be the firstfi “sojourn” site of
layers: the deep, periventricular germinal matrix that migrating cells; STF4 will become the deep white matter;
forms the neurons and glia, the superfi ficial cortical plate and the last-to-form STF6 contributes primarily to cal-
(which will become layers 2–6 of the neocortex), and an losal fibers. These structures are seen well on histologic
intermediate zone. The intermediate zone recently has studies, and STF2 to STF6 can be clearly delineated from
come under particular scrutiny by some groups. Its mi- STF1 superfi ficially and the deeper germinal matrix on
croscopic anatomy reveals a highly complex, regionally pmMR. Areas of regional heterogeneity within STF2 to
specifific pattern called “stratifified transitional fields” by STF6 are seen on pmMR, but how they relate to the his-
Altman and Bayer7,8 and the “transient fetal zones” by tologically defi
fined regions has not yet been determined.
Kostovic et al.9,10 One component of the intermediate It would be of great value if the wealth of information
zone is the huge number of radial glial cells extending from histologic studies on human fetuses could be used to
through the full thickness of the hemisphere. Further- improve our understanding and interpretation of fetal
SE C T I O N A L A N A T O M Y O F T H E F E T A L B R A IN 37
TABLE 2-1 Rados et al. describe the early fetal brain (10–13
Overview of Stages of Development of the Cerebral weeks postovulatory weeks, therefore approximately
Cortex and White Matter 12–15 weeks post last menstrual period) as having the
standard three-layer structure, namely, cortical plate,
Gestational Age
intermediate zone, and ventricular zone. By the midfe-
(Converted to Post
Last Menstrual Period) Main Features
tal period (which they defi fined as 15–22 weeks postovu-
latory weeks, approximately 17–24 weeks post last
Embryonic Phase I: 6–9 weeks Universal embryonic zone menstrual period) the transient zones have developed,
Early fetal Phase II: 10–14 weeks Formation of cortical plate and the authors describe seven layers demonstrable on
Mid fetal Phase III: 15–17 weeks Formation of transient histologic studies. From superficial
fi to deep they are as
fetal zones follows (Figure 2-1):
Phase IV: 18–26 weeks Peak of subplate zone 1. Marginal zone: Not visible in neocortical regions
Late fetal Phase V: 27–38 weeks Dissolution of transient on pmMR studies
fetal zones 2. Cortical plate
Neonate Phase VI Immature six-layer cortex 3. Subplate zone
Modified from Rados M, Judas M, Kostvic I: In vitro MRI of brain development. 4. Intermediate zone
Eur J Radiol 57:187–198, 2006. 5. Subventricular zone
6. Fiber-rich periventricular zone
7. Ventricular zone: Equivalent to the primary
and secondary germinal matrices of Bayer and
imaging studies. Interpretation of MR images without Altman
direct comparison with histologic studies is fraught with Rados et al. place great importance on the subplate zone
problems; fortunately, Rados et al.4 have made significant
fi in the normal development of the cerebral cortex; it
inroads into the subject. Many of the details described reaches its developmental peak at 27 to 30 weeks post-
here are seen well on pmMR images, particularly on the ovulatory weeks (approximately 29–32 weeks post last
coronal sections of 19- to 20-week and 22- to 23-week fe- menstrual period). They note that the subplate is
tuses. Rados et al. used a different nomenclature system the largest single component of the cerebral wall in the
for the transient layers in the wall of the cerebral hemi- second-trimester fetus and that it is proportionally
spheres of the second- and third-trimester fetus than did much larger in human fetuses than in fetuses of other
Bayer and Altman, what might be considered a more mammalian species. Although the subplate does contain
“classic” system. They studied fetuses from all three cell bodies of both neurons and glia, Rados et al. con-
trimesters, and their overall view of the development of sider the subplate to be the major “waiting” compart-
the cerebral cortex is summarized in Table 2-1. ment for fibers that are destined to project to the future
CP
CP
SP
SP
IZ
IZ
SZ SZ
VZ
VZ
G G
TH IC P
A B
Figure 2-1 Transient fetal zones of the developing cerebral hemispheres. A, Coronal T1-weighted image of an 18-week postovulatory
week fixed fetal brain (20 weeks post last menstrual period). B, Histologic section from a 20- to 21-week postovulatory week fi fixed fetal brain
(22–23 weeks post last menstrual period). CP, Cortical plate; IC, internal capsule; IZ, intermediate zone; G, germinal matrix; P, putamen SP,
subplate, SZ, subventricular zone; TH, thalamus; VZ, ventricular zone. (From Rados M, Judas M, Kostovic I: In vitro MRI of brain development.
Eur J Radiol 57:187–198, 2006.)
38 ATL A S OF FE T A L A ND POS T NA T A L BR A IN M R
mature cerebral cortex. They detailed the major axonal and intense regional and temporal variations. Judging by
contributors to the subplate in earlier publications9, the images of the second-trimester fetus shown in the
which include thalamocortical projections, projections Rados paper, T1-weighted images of fixed fi tissue appear
from the basal forebrain, and ipsilateral and cortico– to discriminate between those structures better than T2-
cortical projections via the corpus callosum. It is sus- weighted images of unfixed fi tissue. However, the basic
pected that modeling and parcellation of the future principles appear to hold true: regions with high cellular-
cerebral cortex is instigated at this time. ity (e.g., cortical plate) have comparatively high signal on
The subplate zone also appears to have a signifi- fi T1-weighted images and low signal on T2-weighted
cant effect on the morphologic development of the images, whereas the reverse signal pattern is seen in cell-
sulcal/gyral pattern of the future cerebral cortex. Kos- sparse regions (subplate zone). These features are sum-
tovic cites the following supporting evidence: marized in Table 2-2.
• The subplate zone is much thinner in species that The reasons why the rapid SSFSE T2-weighted se-
have smooth oligogyric brains in mature animals. quences used for in utero fetal imaging discriminate
• Within the human brain, there is greater gyra- between germinal matrix and fetal brain with less clar-
tion in the regions that have the thickest subplate ity than do short echo train length FSE T2-weighted
zone. sequences used for pmMR have already been discussed.
• The frontal lobes continue to develop tertiary gyri Those arguments also hold true for the transient fetal
postnatally, and this is accompanied by persistence structures of the developing cerebral hemisphere. That
of the subplate zone in those regions. is not to say that they cannot be seen in utero, because
Rados et al. used their extensive experience in fetal in some cases they can, but in our experience not in a
histology to explain the signal characteristics of the robust fashion. The development of the germinal matrix
transient fetal layers on MR imaging. It should be and transient hemispheric structures must hold the key
appreciated that major differences exist between their to the abnormal development of many cortical malfor-
methods of pmMR and those we present in this atlas. mations, and this warrants further research and devel-
They performed pmMR on brains that had been fi fixed opment of imaging methods to show those structures
with aldehyde after removal from the body, whereas we with greater clarity. This is not a problem in fetuses
used pmMR on unfixed fi tissue with the fetal brain still postmortem, and interesting features can be shown in
in situ. In those circumstances, they found that T1- developmental abnormalities. An example is shown in
weighted images were best for second-trimester fetuses, Figure 2-2.
whereas T2-weighted images gave better results in Some improvements have been made in delineating
more mature fetuses. In contrast, we used T2-weighted the transient zones of the fetus using iuMR, particularly
sequences throughout the gestational age ranges stud- with refinements
fi of diffusion-weighted imaging (DWI).
ied. In spite of this, similar interpretation of the signal This is a difficult
fi sequence to use in utero but has been
characteristics likely is valid for our studies as well. The shown to be possible by many groups. Most frequently
two regions of the second-trimester fetal cerebral hemi- DWI is performed with an echoplanar imaging method
sphere that have the highest cellular density are the using its “ultrafast” capability. The signal contrast pro-
ventricular zone (germinal matrix) and the cortical duced on DWI and the associated apparent diffusion
plate. Those regions returned high signal on the T1- coefficient
fi (ADC) map is dependent on how freely water
weighted pmMR studies of Rados et al. and low signal can diffuse on a microscopic scale. In regions where
on our T2-weighted pmMR studies. This is not surpris- water diffusion is restricted, DWI shows very high sig-
ing because we know from other imaging studies that nal matched by low-signal (low-diffusion) regions on
regions that have high cellular density and high the ADC maps (Figure 2-3). It is possible that further
nuclear-to-cytoplasmic ratios (e.g., primitive neuroecto- refinement
fi of such techniques will contribute to im-
dermal tumors and lymphoma) have T1 and T2 short- proved early detection of subtle abnormalities of neo-
ening in comparison to normal brain. In contrast, the cortical development.
subplate zone has a high proportion of extracellular
components that are intensely hydrophilic. Therefore TABLE 2-2
the high water content in the subplate zone is respon-
Summary of Signal Characteristics of Different Regions
sible for the low signal on T1-weighted images and the of the Developing Cerebral Hemispheric Wall of the
high signal on T2-weighted images. This is true at least Fetus on Magnetic Resonance Imaging
in fetuses at 30 weeks’ gestation post last menstrual
period, but from then on the disappearance of the ex- Predominant T1W T2W
tracellular, hydrophilic matrix produces blurring be- Zone Histology Signal Signal
tween the subplate and intermediate zone (and to a Cortical plate Cell dense ↑ ↓
lesser extent between the subplate and cortical plate). Subplate Extracellular hydro- ↓ ↑
The appearance of the other transient layers of the philic matrix
second-trimester fetus (intermediate zone, fi fiber-rich peri- Intermediate Cellular ↑ ↓
ventricular zone, and subventricular zone) is more diffi- fi Subventricular Cell sparse ↓ ↑
cult to resolve on MR. This is because of the reduced in- Ventricular Cellular ↑ ↓
herent contrast resolution between the adjacent layers
SE C T I O N A L A N A T O M Y O F T H E F E T A L B R A IN 39
A B
Defect in
intermediate
zone
C
Figure 2-2 Postmortem magnetic resonance imaging of a fetus that underwent spontaneous abortion at 19 weeks’ gestational age. All
images are T2-weighted. A, B, Images in the axial plane at the level of the superior portions of the ventricles. Both hemispheres are abnormal,
showing ventriculomegaly, but the right hemisphere also has a parietal meningoencephalocystocele and an abnormal cleft with an anomalous
venous structure in it adjacent to the right frontal lobe. Note that the intermediate zone is markedly thinner in the right hemisphere which is
shown well on parasagittal imaging (C) along with a focal defect as indicated.
40 ATL A S OF FE T A L A ND POS T NA T A L BR A IN M R
A B
C D
Figure 2-3 Examples of diffusion-weighted imaging in a 22-week fetus with isolated ventriculomegaly. A, B, Single-shot fast spin echo images
in the axial plane through the ventricles. C, D, Equivalent diffusion-weighted images (b ⫽ 1000). Note that the germinal matrix has high signal
on diffusion-weighted images (arrows) indicating low diffusivity, and the subplate has low signal on diffusion-weighted imaging indicating high
diffusivity.
41
42 ATL A S OF FE T A L A ND POS T NA T A L BR A IN M R
Migrating
cells
Germinal
matrix
Caudeate
e Corpus
nucleus
s callossum
Choroid
plexus
Latera al
ventriclle
Corpu us
callossum
Caudeatte Ca
avum septi
nucleu
us pellucidi
La
amina of
Interna
al se
eptum
capsule pe
ellucidum
Putam
men
Thalamus
Corpus
callosum
Migrating
cells
Head of
caudate An
nterior horn
nucleu
us of lateral
ve
entricle
Putam
men A
Anterior thalamic
n
nucleus
Claustrrum V
Ventrolaeral thalamic
n
nuclei
Tail of C
Crus of
caudate the fornix
nucleus
Th
hird ventricle
Spleniumm of
Migrating
ting corpus ccallosum
cells
Genu of corpus
callosum
m
Reticular nucleus
of tthalamus
Glob bus
pallid
dus
Masssa intermedia
Centromedian
C
n
nucleus
Pu
ulvinar
Habenu
ula
Pine
eal gland
d
Hippocampus
Head of caudate
udate
nuccleus
Septal area
Putam
men
Co
olumn of fornix
Claustru
um
Zo
ona incerta
Globus pallid
dus Mammillothalamic tract
M
Centromedian nucleus
Habenulo-interpeduncular
tract
La
ateral geniculate body
Quad
drigeminal plate
Brachium m of
inferior co
colliculus
An
nterior
commiissure Column
n of fornix
Sub
bthalamic nucleus
Optic tract Optic tract
Cerebral peduncle
R
Red nucleus
Ha
abenulo-interpeduncular tract
Germinal Oculo
omotor nucleus
matrix Inferior colliculu
us
Migratting
cells
Migrating ccells
Olfactorry tract
Amygdala
Optic tract
Infund
dibular nucleus
Mamm
millary body
Cere
ebral peduncle
Subsstantia nigra
Su
uperior
ce
erebellar
pe
eduncle
Pons
Principal sensory
nucleus of
n
ttrigeminal nerve
Dentate nucleus
Vestibularr nuclei
Fourth ventricle
Cortex
Germinal
G
m
matrix
Lateral
ventricle
Mig
grating
cells
Corpus callosum
La
ateral ventricle
Caudeate
nucleus
Clausstrum
Puta
amen Germin nal
matrix
Rhinencep
phalic
Internal ca
apsule cavity
Olfactory tract
Cavum septi
pellucidi
Migrating cells
Germinal matrix
Latera
al
cerebra
al
foss
sa
T
Thalamus
Claustrum
m
Coolumn of
fornix
Putamen
Anterior
Third ven
ntricle
comm
missure
Globus pallidus
Caudeate nucleus
Germinal matrix
Interna
al Corp
pus callosum
capsule
e
Third ventricle
Thalamus
Mammillothalamic
tra
act
Column of
Optic
forn
nix
tract
Tela choroidea of
third ventricle
Choroid plexus La
ateral
ge
eniculate
bo
ody
Fimb
bria of
hippoca
ampus
Cerebral peduncle
Hippoca
ampus Pyramida
al tract
Pons
Sub
bstantia nigra
Basilar artery
Red nucleus
Interpeduncular
fossa
Superior
colliculus
Cerebral Inferio
or
aqueduct collicu
ulus
Su
uperior
ce
erebellar
pe
eduncle
Fourth Cerebellum
ventricle
Nuc
cleus of
abducent
nerv
ve
Superior
olive
Pyramid
d
Vertebral
artery
Inferior
olive
Internal capsule
Claustrrum
H
Hippocampus
Olfactorry region
Choroid fissure
Anterior co
ommissure
Lateral genicu
ulate body
Amygdala
Inferior
f horn off
lateral ventricle
Anterior horn of
lateral ventric
cle Posterior horn of
Caudate e lateral ventricle
nucleuss
M
Medial geniculate
b
body
Putamen
Inferior cerebellar
Globus pallidus peeduncle
Denttate nucleus
Flocculuss
Cerebral peduncle
Lateral recesss of
fourth ventricle
Ventrolateral
thalam
thalamic
nuclei
Externall Ce
entromedian
capsule
e nu
ucleus
Head of Pulvinar
caudate
nucleus
Medial
M
g
geniculate
Olfactorry b
body
trac
ct
Subth
halamic nucleus Fou
urth
ventricle
Substantia nigra
Pyramidal tract
Pons
Pariieto-occipital
sulccus
Anterior horn of
lateral ventricle
e Posterior horn of
lateral ventricle
Rhinencephalic Red nucleus
cavity
Infe
erior colliculus
Olfactory tra
act
Optic chiasm Ve
ermis
Cerebral peduncle
Gra
acile nucleus
Pyramidal tract Inferio
or olive
Migrating
cells
Centrum
semiovale
Co
ortex
Ge
erminal
matrix
Caudeate nucleus
Internal ca
apsule
Migrating
cells
Lateral
ventricle
e
Choroid plexus
Head of caudate
nucleus Annterior horn of
latteral ventricle
Puta
amen
La
amina of
septum
Claustrrum pe
ellucidum
Fornix
In
nterventricular
Globus pallidus fo
oramen
(of Monro)
Thhird ventricle
Tail of caudate
nucleus
Thalamus
Choroid plexus of
lateral ventricle
Germina
al matrix
Fascio
olar gyrus
Lamina
terminalis
Column of Third ventric
cle
forn
nix Putame en
Anterrior commissure
Mammillothalam
mic Gllobus pallidus
tra
act Subthalamic nucleus
Retrolenticular limb of
internal capsule
Lateral geniculate body
L
M
Medial geniculate body
Hippocampus
Cereb
bral aqueduct
Quadrigeeminal plate
Nucl. ruber et fasc. retroflexus
Optic
recess
Infundibular nucleus
Olfactory tract Optic tract
Mammillary b
body
Amygda
ala
Germinal matrixx Anterior
A
c
commissure
Cornu ammonis Fimbria of
hippocampus
Superior cere
ebellar
Limbus
s peduncle
Giacomin
ni
Inferior colliculus
Substanttia nigra Vermis
Pons
Superior
olive
Inferiorr
cerebellarr M
Middle cerebellar
peduncle e p
peduncle
Nucleus of
abducent nerve
a
Cochlear
nucleus
Dentate nucleus
Vestibular
nuclei
Fourth Cerebella
ar
ventricle Vermis hemisphere
Migrating
cells
Cortex
Germin
nal matrix
Bodyy of corpus
Head of caudate callossum
nuccleus
A
Anterior horn of
llateral ventricle
Internal capsule
Cavum septi
pellucidi
Putamen
n
Rosstrum of
corp
pus callosum
Claustru
um
Olfactory tract
Migrating cells
Caudate
e nucleus
Internal capsule
Putamen
Fornix
Insular corttex Anterior thalamic
nucleus
Claustru
um
Third ventricle
T
Globus pallidus
Co
olumn of fornix
Anterior commissure
Am
mygdala Hypotha
alamus
Optic tract
Thalamostriate vein
M
Migrating
Middle cerebrral ce
ells
artery
Subthalamic
us
Thalamu nucleus
Optic tract
Anterrior
commissu
ure
Globus pallidus
Germinal matriix
Reticcular nucleus
of thalamus
Internal capsule
Massa intermedia
Su
ubthalamic nucleus
Cerrebral peduncle
Germinal matrix
Mammillary body
Inferior horn of
lateral ventricle
l Hippocampus
Falx
Fourth ventricle
Vermis
Dentate nucleuss
Cerebellar
hemisphere
Lateral recess of
choroid plexu
us Floc
cculus
Laterral recess of
Pyramid fourth
h ventricle
Inferior olive Glossopharyngeal nerve
Glossophar
Internal capsule
Transverse ceerebral
Putamen fissure
Globus pallidus
Choroidal fissure
fissur
Inferior horn of
lateral ventricle
Ventrolateral thalamic
nuclei
Head of caudate nucleus G
Germinal
i l matrix
ti
Chorooid plexus of
lateral ventricle
M
Medial geniculate
bo
ody
Anterior horn of Posterior horn of
lateral ventricle lateral ventricle
Cerebellar hemisphere
Subthalam
mic nucleus
Denttate nucleus
Cerebral peduncle
Tentorium Flocculuus
Lateral recess off
Cochlear
C hl nucleus
l fourth ventricle
Interventricular foramen
((of Monro))
Cavum sep
pti pellucidi Internal cerebral vein
Column of fo
ornix Splenium of ccorpus callosum
Supprapineal recess
Greeat cerebral vein
Ante
erior (of Galen)
commisssure
Quadrigeminal
Q
pllate
Third ventricle Vermis
Red nucleus
Chhoroid plexus of
fou
urth ventricle
Pyramidal tract Cunea
ate nucleus
Inferior olive
Thalamus
Th
hird ventricle Velum interpositum
Cavum verrgae
Cavum se epti
pelluccidi Suprapineal recess
Genu of corp
pus Pinea
al gland
callosum
Poste
erior commissure
Ce
erebral aqueduct
Pyramidal tract
IInferior
f i olive
l
Co te
Cortex
Migra
ating cells
Germinal
G
m
matrix
Central
sulcus
Centrum
semiovale
Germinal matrix
Corpus callosum
Caudate nucleus
Internal
capsule Cavvum septi pellucidi
Radiation of
corpus callosum
Choroid plexus of
lateral ventricle Migrating
cells
Putamen Area se
eptalis
Glo
obus pallidus Colu
umn of fornix
Cla
austrum Massa intermedia
M
Mammillothalamic tract
Germinal
minal matrix
Anterior horn of latera
al ventricle
Internal capsule
Zona incerta
Ante
erior commissure
Co
olumn of fornix
Gangliothalamic body
Ma
ammillothalamic tract
Ventrolateral thalamic nuclei
Germinal matrixx Centromedian nucleus
C
Haabenulo-interpeduncular tract
Hippocampu
us Subccommissural organ
Pulvinar
Olfactory tract
Middle cerebra
al artery Optic re
ecess
Ante erior cerebral artery
Amygd
dala Optic tract
O
Hippocampu
us Mammillary body
Cerebral peduncle
Inferior horn off
lateral ventricle Basal vein
De
ecussation of
su
uperior cerebellar
pe
peduncle
Hippocampal sulcus
Pyramidal
y tract
Motoor nucleus of
Medial lemniscus trigeminal nerve
Principal sensory
nucleus of
trigeminal nerve
Dentate nucleus
Anterior hornn of
lateral ventricle
Head of caudate
e
nucleus Corpus
C
ca
allosum
Cavum
Internal caps
sule septi
pellucidi
Puta
amen
Germ
minal matrix
Olfactory tract
Germinal
rminal
matrix
Body of caudate
nucleus
Fo
ornix
Laterall Anterior thalamic nuclei
A
sulcuss
Ventrolateral thalamic nuclei
Claustrumm R
Reticular nucleus of thalamus
Globus pallidus
s Mammillothalamic tract
Hyypothalamus
Anterior commiss
sure
Coluumn of fornix
Amygdala Optic chiasm
c
Germinal
matrix
Migratting cells
Germinal matrix
Medullary stria
of thalamus
Medial thalamic nuclei
M
Ventrolateral thalamic
nucle
ei Massa intermedia
M
Centromedia an Z
Zona incerta
nucleus
Subthalamic nucleus
Germinal matrixx
Optic tract
O
Inferior horn of
lateral ventric
cle A
Amygdala
Hippocampus Mammillary
body
Cavum verrgae
Tail of caudatte
nucleu
us
Crus off the fornix
Lateral & Medial In
nternal cerebral vein
geniculate bodyy H
Habenula
Centromedian nucleus
C
Tail of caudatte
nucleu
us Lateral geniculate body
Fimbria of
Cornu ammonis
hippocampu us
D
Dentate fascia
Substantia nigra
Red
ed nucleus Oculomoto
or nerve
Cerebral
peduncle
Migratiing
ce
ells Sp
plenium of
co
orpus callosum
Germinall
matrixx Ce
erebral aqueduct
Chorooid
A
Alveus
plexxus
Cornu ammonis
M
Medial longitudinal
fa
asciculus
Pyramidal
y tract
Pons Trigeminal
nerve
Indusium griseum
Fasciolar gyrus De
entate gyrus
Hippocampus
Inferior colliculus
Lateral lemniscus
Fallx P
Posterior horn of
la
ateral ventricle
Calcarine sulcus
Globose nucle
eus
De
entate nucleus
Lateral
sulcus
Lateral
Germinal ventricle
matrix
Migrating
M
c
cells
Posterior
P
horn of
h
l
lateral
amen
Puta Pulvinar v
ventricle
Glob
bus pallidus Transverse cerebral fissure
Inferior horn of Lateral geniculate body
lateral ventricle
Lateral
ventricle Thalamus
Germinal
al
matrixx
Olfactory
Inferior
tract
colliculus
Optic tract F
Fibres of
Cerebral peduncle ffacial nerve
Pyramidal tract Choroid plexus of
Superior olive fourth ventricle
Fibres of abducent
nerve C
Cuneate nucleus
Inferior and fasciculus
olive
Corpus
us callosum
Third ventricle
Lateral ventricle
Pineal g
gland
Anterior commissure
Column of fornix Ce
erebral aqueduct
Mammmillary body Fourth ventricle
Pyramidal tract
Great longitudinal
fissurre Falx
fissure
Germin
nal
nal
matrix
Central
sulcus
Ce
entrum
entrum
sem
miovale
Anterior cere
ebral artery
Lateral
ve
entricle Indu
usium griseum
Corpus callosum
L
Lamina of
septum
p
pellucidum
Cavum septi
pelllucidi
Caudate
nucleus Co
orpus
callosum
Claustrum
Indussium
grise
eum
Germin nal
matrix
Splenium of
corpus callosum
Germ
minal
matrix
Anterior hhorn of
Insular lateral ven
ntricle
cortex
Area sep
ptalis
Globus Columnn of fornix
pallidus
Third ve
entricle
Mamm
millothalamic tract
Interna
al
capsule
e Ventrolateral thalamic nuclei
Cen
ntromedian nucleus
Pulvinar
Fimbria off
hippocampuss
Splenium of
Fasciolar corpus callosum
gyruss
Germinal
matrix
Puta
amen
Anterior com
mmissure
Lateral partt of
globus pallid
dus Column of
o fornix
Zona in
ncerta
Medial part of
globus pallidus
s Mamm
millothalamic tract
Ventro
olateral thalamic nuclei
Centtromedian nucleus
Head of caudate
e P
Pulvinar
nucleuss
H
Hippocampus
D
Dentate fascia
Germinal matrix
H
Habenula
Choroid plexus of
lateral ventric
cle
Uncus
Inferior horn of Gyrus rectus
lateral ventricle Olfactory tract
Anterior Germinal matrix
commissure
Optic radiation
Optic tract
Limbus Mammillary body
Giacomini
Cerebral peduncle
Cornu Substantia nigra
ammonis
Fibres of oculomotor nerve
Dentate
fascia Nucleus of trochlear nerve and
medial longitudinal fasciculus
Hippocampus Inferior colliculus
Posterior horn of
lateral ventricle
Medial longitudinal
Trigeminal nerve fasciculus
Middlee cerebellar
peduncle
Superior
vestibular
Inferior cerebellar
nuclei
peduncle
Noduluss
Uvula Dentate
D
n
nucleus
Pyramid
Globose
nucleus
In
nferior olive
Floccu
ulus
Glossopharyngeal
nerve
Spinal tract of
trigeminal nerve
N
Nucleus of
h
hypoglossal nerve
Area po
ostrema
Cuneate nucleus
Migrating cells
Germinal matrix
Germ
minal matrix
Corpus calllosum
H
Head of caudate
n
nucleus
IInternal capsule
Putamen
Anterior
thalamicc
nuclei
Ge
erminal matrix
Reticular nucleus
of thalamus Corpus callosum
C
Trigone of the
lateral ve
entricle
Tentorium
Hipp
pocampus
Inferior colliculus
Lateral lemnis
scus
hlear
Fibres of troch
nerve Medial longitud
dinal
fasciculus
Pyramida
al tract Trigeminal nerve
nerv
Pons
Fastigial
g nucleus
Vestibular nuclei
Denttate nucleus
Inferior cerebellar
peduncle
Germinal
matrix Crus of the ffornix
Caudate
e nucleus
Trigone of
o the
Internal cap
psule lateral ventricle
Centrum
m Calcaarine sulcus
semiovale
e Migrating cells
Posterior horn
of lateral ventricle
Putam
men Pulvinar
Globuss pallidus Lateral geniculatee body
Anterio
or commissure Hippocampus
Amygdala IInferior
f i horn
h off lateral
l t l ventricle
t
Centrum
semiovale
Thalamostriate vein
Head of cauddate
nuccleus Corpus callosu
um sulcus
Anterior Pa
arieto-occipital
horn s
sulcus
of lateral
ventricle
Calc
carine sulcus
Internal
capsule Pulvina
ar
Putam
men Centromedian nucleus
Subbstantia innominata
Ventrolate
eral thalamic nuclei
Middle cerebral artery Substantia n
nigra
Hippocampall Subthalamic n
Amygdala Hi nucleus
sulcus
Anterior
Vein of septum thalamic
nucleus Medial
pellucidum
thalamic
th l i
Cavum seepti nuclei
pelluccidi Cavum verga
ae
Spleniumm of
corpus ca allosum
Inferior colliculus
c
Germinal Latera
al lemniscus
matrix
Op
ptic tract
Dentate
Red nucleus
nucleus
Ce
erebral peduncle
Flo
occulus
Fibres of trigeminal nerve
Cavum
Lateral ventricle vergae
Cavum septi Sple
Splenium of
pellucidi corp
pus callosum
Genu of corpuss Postterior
callosumm commissure
Anterior commissure Medial
longiitudinal
Column of fornix fasciculus
Mammillary body
Red nucleus Choroid plexus of
Oculomotor nucleus ffourth ventricle
Pons
Pyramidal tract
Great longitudinal
fissure
Germ
minal
matrix
x
Late
eral
ven
ntricle
Post-
central
sulcus
Centrum
C t
semiovale
Germinal matrix
Latteral
venttricle
Caudate
e Inddusium
nucleus
s grriseum
Subependymaal
vein
n Corpus
callosum
In
ndusium
g
griseum
Germinal
matrix
Choroid plexus
Anterior horn of
lateral ventricle
Head of caud
date
nucle
eus Cavum septi pellucidi
Veinn of septum
Germinal pelllucidum
matrix
Lammina of septum
pellucidum
Lateral
sulcus
Internal cerebral
v
vein
Velum
Claustrum
m interpositum
Choroidal
fissure
Crus of
the fornix
en
Putame
Cavum vergae
Cavu
Thalamus
Posterior limb
b of Third ventricle
internal capssule Ma
assa intermedia
Ventrolaterral Thirrd ventricle
thalamic nuclei Meddullary stria of
thala
amus
Medial thalam
mic
nucclei Internal cerebral
Pulvinar vein
Crus of the fornix
C
Trigone of thee
lateral ventricle
e R
Radiation of
co
orpus callosum
Glomu us of
choroid plexus
Splenium of
corpus callosum
Fimbria of hippocamp
pus Sple
enium of
corp
pus callosum
Posterrior horn of
laterall ventricle
i l Fasciolar gyrus
Anterior commis
ssure
Germ
minal matrix
Lamina terminalis
Medial medullaryy
lamina of globuss Third ventricle
T
palliduss C
Column of fornix
Mammillothalamic
M
Subthalamiic trract
nucleuus
Lateral geniculate
body Posterior commissure
Subcommissural organ
S
Germinal matrix
Ce
entromedian nucleus
Hippocampu
us Pulvinar
Calcarine sulcus
Posterior horn of
lateral ve
entricle
Nucleus accumbens
Ansa lenticularis
Anterior perfora
ated Germin
nal matrix
substance
Substan
ntia
innomina
ata
Hypotthalamus
Anterrior
commissuure Column of fornix
C
Red nucleus
R
Putamen
n
Medial part of
globus pallidus
Cerebral
aqueduct
x
Germinal matrix Suuperior
co
olliculus
Subthalamic
nucleuss
Olfa
actory sulcus
Olfactory tract
Gyrus re
ectus
Middle cerebral
artery Optic
O ti chiasm
Optiic tract
Inferior horn of
lateral ventricle Hypothalamus
Mammillary body
M
Red nucleus
Hippocampus
Hippocampa al
sulcuss
Culme
en
Posterior horrn of
lateral ventricle
i l
Medial
longitudinal
fasciculus
Pons Vesttibulomesencephalic
Medial lemniscus tractt
Inferior
Lateral lemniscus
cerebellar
peduncle
Dentate
Fourth ven
ntricle nu
ucleus
Emboliform
Embo
Fastigial nucleus
nucleus
Inferior cerebella
ar
pedunclee
Medial lemniscus
Vestibulocochle
ear nerve Basilar artery
Fibress of
facial neerve
Ventral cochlea
ar
nucleuss
Flocculus
Inferior cerebella
ar
peduncle Cuneate
nucleus
Spinal tract of
trigeminal nerve
Migrating cells
Germin
nal matrix
Olfactory sulcus
Germinal matrix
Head of caudate
nucleus
Bo
ody of corpus
psule
Internal cap callosum
Anterior horn of
lateral ventricle
Putame
en
Cavum septi pellucidi
C
Claustru
um
Ro
ostrum of
co
orpus callosum
Internal Anteriior cerebral artery
capsule
Olfactory tract
Globus pallidus
Corp
pus callosum
Insular cortex
Lateral sulcus
s Interventricular
foramen
Column of fornix
C
Anterior commissure
A
T
Third ventricle
Optic chiasm
Amygdala Substantia
Uncus innominata
Body of caudate
nucleus Massa intermedia
Mas
Fornix
Third ventricle
Subthalamic nucleus
Medial medullary
Perfora
ating lamina of
fib
bres globus pallidus
Ansaa lenticularis
Inferio
or horn of
latera
al ventricle
Hippoca ampus
Posterior cerebral artery
Cerebral peduncle
Internal
cerebral
vein
Posterior commisssure Third vventricle
Medial longitudinaal
Cerebral
C
fasciculuss
a
aqueduct
Fibres of Medial lemniscus
oculomotor D
Decussation of
nerve ssuperior cerebellar
p
peduncle
Trigeminal ne
erve
Pyra
amidal tract
Pons
La
ateral
ven
ntricle
Calcarine sulcus
Vermis
Superior cerebellar
pedunncle
Denttate nucleus Infferior cerebellar
peeduncle
In
nferior olivary nucleus
Pyramid
Medial and dorsal
accessory olivary nucleus
Posterior horn
of lateral
al
ventricle
Calcarine sulcus
Calcar avis
Dentate nucleus
Horizontal fissure
Glomus of
choroid plexus
Pu
ulvinar
Medial medullaary lamina
us pallidus
of globu
Media
al geniculate body
Ansa lenticularis
Calcarine
Anterrior sulcus
commissuure
Glob
bus pallidus
Cerebral
Optic tract
peduncle
Subthalamic nucleus
Corpus
callosum
Cavum septi
epti
pelluccidi
Cavum vergae e
Pineal gland
Ante
erior
commiss
sure Cerebral aqueduct
Centrum semiovale
Central
sulcus
Somatosensoory
radiatio
on
Postcentral
su
ulcus
Germinal matrix
Lateral su
ulcus
Anterior cerebral artery
A
Lateral ventricle
e
Posterior limb of
internal capsule
Corpus callosum
C
Germinal matrrix
Head of caudate
udate nucleus Genu of corpus
p callosum
Anterior horn
Laterral sulcus of llateral ventricle
Ca
avum septi pellucidi
Vein of septum
Putam
men pellucidum
Inte
ernal cerebral vein
Germinal matriix
Velum interpositum
V
Cavum vergae
Thalamus
Choroid plexus of
lateral ventricle
Germinal matrix
Thalamostrriate vein
Annterior horn of
latteral ventricle
Anterior thala
amic
nucleus
Column of fornix
C
Insular cortex
Interventricular
foramen
Posterior limb of Third ventricle
internal capsuule
Choroid plexus
of third ventricle
o
Spllenium of
corrpus callosum
Choroidal fissurre
Germinal matrix
Puta
amen
Anterio
or commissure
Globus pa
allidus
Ventrolateral thala
amic
nu
uclei Co
olumn of fornix
Centromedian Massa
nuccleus intermedia
Habenula
Posterior limb of
internal capsule Internal cerebral
vein
Chhoroid plexus of
Pulvinar third ventricle
Splen
nium of
Glo
omus of corpu
us callosum
choroid
d plexus
l
Oculomotor
Amygddala nucleus
Inferior horn of Ce
erebral peduncle
lateral ventricle Superior cerebellar peduncle
S
Hippocampu us
Posterior ho
orn of Cere
ebellum
lateral venttricle
Basilar
artery Medial longitudinal
Trapezoid body fasciculus
Medial lemniscus Nucleuss of
abduceent nerve
Trigeminal nerve
Fibres of
Motor fibres of
ab
bducent
trigeminal nervve
ne
erve
Dentate nucleus
Inferior cerebellar
peduncle
Emb
boliform nucleus
Nodulus Horizo
ontal fissure
Uvula
Pyramid T b
Tuber
Migrating
g g cells
Germin
nal matrix
Olfactory sulcu
us
Olfactory tract
Corpus
p callosum
Germinal matrix
Head of cau
udate
nuccleus Cavum septi
s pellucidi
A
Anterior horn of
la
ateral ventricle
Lamina of septum
L
p
pellucidum
Putamen
External capsule
e
An
nterior commissure
Claustrum
m
Substantia innominata
Globus pallidus
Anterior perfo
orated
substtance Optic chiasm
Infundib
bulum
Amygdala Uncus
Middle cerebral artery
Germinal matrix
Medial medulla
ary Fornix
lamina of glob
bus
pallid
dus Cauda
ate nucleus
Lateral sulcus Th
hird ventricle
Lateral part of globuss C
Claustrum
palliduss
Medial part of globuss Putamen
palliduss
Anterior
A
Ansa lenticularis c
commissure
Supraop ptic Am
mygdala
commissu ure
Inferior horn of Optic tract Uncu
us
lateral
ateral ventricle Column
Mammillary of fornix
body
Third
ventricle Habenulo-interpeduncular
tract
Posterior commisssure Medial longitudinal
fascic
culus
Cerebral aqueductt
Medial and lateral
geniculate body
B
Brachium of
Superior cerebellar pedu
uncle inferior colliculus
Lateral lemniscus
Fibres of trigeminal nerve
Flocculus
Supe erior olive
Medial lemniscus
Suprapineal
pineal recess Coorona
andd pineal body rad
diata
Superior medu
ullary velum
Inferior colliculus
Superior cereb
bellar
pedu
uncle
Vestibular fibres of
vestibulocochlear nerve Inferior
cerebellaar
Ventral coch hlear nucleus peduncle e
Spinal tract of triigeminal nerve
Inferior olive
Pyramidal Medial
decussation longitudinal
fasciculus
Splenium of
corpus
callosum Cavum
m vergae
Cruss
of thee Pulvvinar
fornix
x
Infferior colliculus
Fimbria of Superior
hippocampuus cerebellar
peduncle
Inferior
Nodulus ccerebellar
ppeduncle
Den
ntate nucleus
Cuneate n
nucleus
Central sulcus
Somatosensory
nsory radiation
Posterior limb of
internal ca
apsule
Germ
minal matrix
Putame
en Tail of caudate
nucleus
Globus
pallidus
Posterior horn
of lateral
Anterio
or ventricle
commissure
Calcarine sulcus
Lateral genic
culate Hippocampus
body Inferior horn of
lateral ventricle
Perforating
Caudate fibres
nucleus Lateral ventricle
Germinal matrix
x Crus of the fornix
Thala amus
Lateral part of
globus pallidus
Putamen
Infe
erior cerebellar
Medial part of pedduncle
globus pallidus
Ansa lenticularis
Cerebellar
Optic tract hemisphere
Sub
bthalamic nucleus
Cerebral peduncle Dentate nucleus
Flocculus
Germinal
minal matrix Crus of the fornix
Lateral ventrricle
Head of caudate Thalamuss
nucleus
Quadrigeminal
plate
Anterior commissure Laterral
lemniscus
Red
d nucleus
Medial lemniscus Inferior
cerebellar
peduncle
Spinal tract of
trigeminal nerve
SECTIONAL ANATOMY
OF THE POSTNATAL BRAIN
This section discusses the normal magnetic resonance nigra have low T2 signal in older children and adults
(MR) imaging appearance of the brains of children but not in neonates or infants.
after term delivery up to the age of 18 months. We illus- A good example of the competing signal changes
trate this topic with anatomically matched T1- and brought about by these mechanisms is illustrated by the
T2-weighted images and the equivalent line diagrams T2 signal of the globus pallidus and putamen at differ-
taken from the 40-week fetus in the Larroche atlas. The ent ages. These structures provide useful comparison
most obvious macroscopic changes that occur at this because they are both deep gray matter nuclei and their
time relate to the normal, sequential changes in the close anatomic proximity allows direct comparison. The
degree of myelination of the brain structures. At its two structures would be predicted to have similar signal
simplest level, MR images can be thought of as maps of characteristics because they have similar neuronal/glial
body water and fat, and the changing proportions of composition. This is true for the first
fi 30 to 32 weeks of
water and lipid in brain resulting from myelination are gestation. However, myelination proceeds more rapidly
well seen on MR images. Several groups have pub- in the globus pallidus when compared with the putamen
lished data on the normal milestones of myelination (even in the posterior portion of the putamen that my-
and have shown how that knowledge can be used in the elinates first). This difference usually can be seen as
early detection of diseases characterized by abnormal lower signal in the globus pallidus on T2-weighted im-
amounts or forms of myelination.1,2 ages at 33 to 34 weeks’ gestational age. As myelination
In the light of several years of teaching trainee radi- proceeds in both structures, the signal differential re-
ologists, two signifi ficant, recurring misconceptions duces, and at 0 to 1 months post term little signal differ-
about brain myelination warrant further discussion. ence is seen, a characteristic that is maintained for a
First, most newcomers to the field fi believe that no number of years. The accumulation of iron in brain
myelin at all is present in the brain of the term neo- structures is exceptionally variable by region and con-
nate, but this is not correct. Second, most newcomers tinues throughout life. MR techniques that can quantify
do not appreciate that the deep brain nuclei or deep the amount of iron deposition are available.3 However,
“gray matter” regions of the mature brain such as the the globus pallidus accumulates iron particularly rap-
putamen and thalamus, contain a relatively high pro- idly and to high concentration. A higher concentration
portion of myelin as well as cell bodies. The myelin is of iron is present in the normal adult globus pallidus
mainly located on projectional axons and interneu- than in the liver. After 7 to 8 years of age, the globus
rons. As a result, gray matter regions change their MR pallidus usually has lower signal than the putamen on
signal intensities during prenatal and postnatal life T2-weighted images, a feature that is most marked on
because of accumulation of myelin in them as well as imaging at higher field strengths (e.g., 3 T).
in adjacent typical “white matter” structures. The sig- Macroscopic myelination before term has been stud-
nal characteristics in the deep gray matter structures ied using both fixed and appropriately stained fetal
are complicated further in later childhood as iron tissue and MR imaging. Good correlation between the
accumulates in the basal ganglia. These changes are two techniques has been observed, particularly if in-
often first seen around the age of 8 to 9 years, with creased signal on T1-weighted images is used to evalu-
rapid accumulation in the second decade of life. The ate early postnatal myelination. Evidence of supraten-
iron is stored in a form that has significant
fi effects on torial myelination is unusual in the 29- to 30-week
T2 (particularly T2′) relaxation, which explains why fetus/premature baby. Consistent evidence of supraten-
structures such as the globus pallidus and substantia torial myelination at any site is seen on MR imaging
153
154 ATL A S OF FE T A L A ND POS T NA T A L BR A IN M R
only at 33 to 34 weeks. High T1 signal at that stage low T2 signal due to myelin formation in the 38-week
is frequently seen in the thalamus (particularly ventro- fetus. It has been postulated that there is a selective vul-
lateral) and putamen (particularly posteriorly); the nerability for regions of the brain that are metabolically
lateral thalamic regions and globus pallidus may also active in the face of hypoxia/ischemia. In the brain of the
show reduced signal on T2-weighted images. By 37 to term neonate this does not necessarily imply neuronal
38 weeks, the high T1 signal intensity has increased activity; it is much more likely that myelination is the
generally in the basal ganglia and thalami, and evi- most energy-dependent process. This goes a significant fi
dence of myelination in the posterior limb of the inter- way towards explaining the pattern of injuries seen on
nal capsule and the corona radiata close to the ventri- neuroimaging and this has helped to explain why some
cles is seen. Most of those regions also return low less-well described regions of the brain, such as the ante-
signal on T2-weighted images around that maturity rior lobule of the cerebellar vermis3,4 and the subthalamic
(Figure 3-1). nucleus,5 are also involved in the process. Our interest in
Myelination is more advanced in the infratentorial the involvement of the subthalamic nucleus in cases of
brain structures. By 33 to 34 weeks, prominent signal profound hypoxic ischemic injury has come about
changes consistent with myelination on both T1 and because of the central role of that structure in suppressing
T2 sequences are seen in most of the dorsal pons and unwanted movements acting in parallel to volitional
medulla and in the deep cerebellar white matter. High- movement. It is no surprise to fi find that the subthalamic
resolution studies show myelination within the inferior nucleus myelinates close to term (Figure 3-4).
colliculus and medial lemniscus. By 37 to 38 weeks, Detailed descriptions of myelination can be reviewed
prominent myelination usually is seen in the superior in other more specific fi texts,1 but using the physical
cerebellar peduncle, most of the midbrain, and the explanations outlined earlier in the introduction we can
cerebellar white matter. A 38-week example is shown in produce a list of key features that may be useful in
Figure 3-2. clinical practice.
There is close correlation between the regions of the • Mature myelin has high signal on T1-weighted
brain injured close to term by profound, hypoxic ischemic images (compared to gray matter).
injury and the regions of the brain that are actively my- • Mature myelin has low signal on T2-weighted
elinating. For example, a typical textbook description of a images (compared to gray matter).
close-to-term profound ischemic injury includes involve- • T1-weighted images should show the expected high
ment of the lateral thalamus, posterior putamen, white signal in all white matter regions by the age of
matter of the paracentral lobule, and optic radiations 8 months (i.e., myelination is virtually adult pat-
(Figure 3-3).1,2 These are precisely the regions that show tern at 8 months).
A B
Figure 3-1 T2-weighted images of the supratentorial brain from a postmortem magnetic resonance imaging study of a 38-week fetus with
normal brain anatomy performed at 3 T. Note the low-signal regions that are most prominent within the lateral thalamus, globus pallidus,
putamen (A), and central corona radiata (B).
S E C T I O N A L A N A T O M Y O F T H E P O ST N A T A L BR A IN 155
A B
Figure 3-2 T2-weighted images of the infratentorial brain from a postmortem magnetic resonance imaging study of a 38-week fetus with
normal brain anatomy image performed at 3 T. Note the low-signal regions that are most prominent within the dorsal brainstem, superior
cerebellar peduncle (A), and anterior lobule of the cerebellar vermis (B).
A B
Figure 3-3 Three-year-old child with dyskinetic cerebral palsy due to profound hypoxic ischemic injury at birth (38 weeks’ gestation). A, Axial
T2-weighted image at the level of the basal ganglia/thalami showing gliosis (high signal) in the posterior putamen and ventral lateral thalamic
nuclei. B, Axial fluid attenuation inversion recovery (FLAIR) image toward the vertex showing gliosis in the paracentral white matter. The affected
regions were actively myelinating at the time of the injury, which may contribute to the selective vulnerability of those structures.
156 ATL A S OF FE T A L A ND POS T NA T A L BR A IN M R
A B
C
Figure 3-4 T2-weighted postmortem magnetic resonance images of a 38-week fetus at 3 T with no structural brain abnormality showing
myelination in the subthalamic nucleus (arrow) in the axial (A), coronal (B), and parasagittal (C) planes.
S E C T I O N A L A N A T O M Y O F T H E P O ST N A T A L BR A IN 157
TABLE 3-1
Checklist for Normal Myelination: Structures That Should Appear Myelinated by the Specified
fi Age
T1 T2
0–1 Month
Dorsal brainstem Dorsal brainstem
Inferior and middle cerebellar peduncles Inferior cerebellar peduncles
Superior cerebellar peduncles and decussation Superior cerebellar peduncles and decussation
Ventral lateral thalamus Ventral lateral thalamus
Posterior putamen Posterior putamen
White matter of pre and postcentral gyri White matter of pre- and postcentral gyri
Optic tracts Optic tracts
Posterior limb of internal capsule Posterior limb of internal capsule (patchy and limited to posterior region)
Central portion of centrum semiovale
Optic radiations
3–4 Months
All of the above All of the above
All of the cerebellum Middle cerebellar peduncle
Ventral brainstem Ventral brainstem
Calcarine fissure white matter Calcarine fifissure white matter
All subcortical motor pathways Optic radiations
Anterior limb of internal capsule
Splenium of corpus callosum
6 Months
All but subcortical white matter Centrum semiovale
All of posterior limb of internal capsule
Patchy changes in anterior limb of internal capsule
Splenium of corpus callosum
Patchy changes in genu of corpus callosum
9 Months
Adult pattern Genu of corpus callosum
Centrum semiovale
12 Months
Adult pattern All of internal capsule
All of corpus callosum
Paracentral and optic radiations/paracalcarine white matter
18 Months
Adult pattern Adult pattern except most peripheral cortical white matter
Peritrigonal white matter can return high signal until the fourth decade (terminal
myelination zones)
• T2-weighted images should show the expected • T1-weighted images are best for assessing my-
low signal in all white matter regions by the age of elination before the age of 8 months (except brain-
24 months (except peritrigonal “terminal myelina- stem and cerebellum) and T2-weighted images
tion” zones). thereafter, although both should be acquired and
• Myelination proceeds in an anatomically predict- compared.
able fashion in normal children, a process that must
The remainder of this chapter demonstrates T1- and
be understood by anyone reporting MR examina-
T2-weighted images from birth to 18 months in order to
tions in children at this age. See Table 3-1.
show the evolution of myelination.
Line Diagram
159
160 ATL A S OF FE T A L A ND POS T NA T A L BR A IN M R
Central
sulcuss
Body of lateral
ventricle
Centrrum
semiovvale
Head of caudate
nucleus
Great longitudinal fissure
Corpus callosum
Anteerior horn of
lateral ventricle
Thalamostriate
e
veinn Ca
avum septi pellucidi
Ve
ein of septum
pe
ellucidum
Thalamus
Corpu
us callosum
Tail of caudate
nucleus
Choroid plexus of
lateral ventricle
Colum
mn of fornix
Genu of corpus callosum
Interventricular foramen
(of Monro)
Ve
ein of septum pellucidum
T
Thalamostriate vein
Puttamen
Choroidal vein
C
us
Globus pallidu Ve
entrolateral thalamic nuclei
Me
edial thalamic nuclei
Claustrrum
P
Pulvinar
Internal capsule
Crrus of fornix
Cavum vvergae
Splenium oof
corpus callo
osum
Glomus of choroid
d plexus
Massa intermedia
Centromedian nucleus
Ventral posterolateral Internal capsule
nucleus of thalamus
Pulvinarr
Choroid plexus of
lateral ventriclle
Optic radiation
O
Fasciolar gyrus
Posterrior horn of
lateral ventricle
Habenula
Ansa lenticularis
sure
Anterior commiss
Subthalamic nucleus
Medial lemniscuss
Red nucle
eus
H
Hippocampus
Medial longitudinal fas
sciculus
De
entate fascia
Optic recess
Op
ptic tract
Infundibulum
Uncus
s Mammillary body
Dentate fascia
a
Nu
ucleus of trochlear nerve and
me
edial longitudinal fasciculus
Limbus Giiacomini
Substantia nigra Inferior colliculus
Optic chiasm
Cerebral peduncle Oc
culomotor nucleus
Pyramidal tract
Medial lemniscus
D
Decussation of superior
cerebellar peduncle
c
Lateral lemniscu
us
Mesencephalic tract
m)
Central lobule (of cerebellum
of ttrigeminal nerve
Decussation of sup
perior
cerebellar pedu
uncle Deccussation of
troc
chlear nerve
Pyramidal
y tract
Trigeminal nerve
Medial lemniscus
Late
eral lemniscus
Vestibulomesencephallic tract
Cen
ntral tegmental tract
Fourth ventriclle
Superior cerebellar peduncle
Uvula
a
Vermis
ermis Dentate nucleus
Medial longitudinal
g fasciculus Pons Pyramidal tract
Medial lem
mniscus
Trapezoiid body
Trige
eminal nerve
Princiipal sensory nucleus
Vestibular nu
uclei of trig
geminal nerve
In
nferior cerebellar
peduncle
Nodulus
Uvula
a Dentate nucleus
Pyram
mid
Medial lemniscus
Trapezoid body Pyramidal tra
act
Superrior olive
Floccculus
Sp
pinal tract of trigeminal nerve
Vestibular nucleii
Inferior cerebellar peduncle
Nodulus
Uvula Dentate nucleus
Pyram
mid
Centrum semiovale
Olfactory sulcus
Olfactory tract
Third venttricle C
Claustrum
Glo
obus pallidus
In
nfundibulum
Amygdala
Uncus
Supraoptic
ptic commissure O
Optic
ti Substantia
tract innominata
Subthalamic nuc
cleus
Inferior ho
orn of lateral ventricle
Cerebra
al peduncle
Hippocampus
Mammillary
M ill body
b d
Hippocampal
sulcus
P
Precentral
t l gyrus
Corpus callosum
Intternal capsule
Fornix
Subthalamic nu
ucleus
Red nucleus
Optic tract
Pyramidal tract
IInterpeduncular
t d l ffossa
Postcentral gy
gyrus
Cing
gulate gyrus
Corpus callosum
P
Pulvinar
Superior collliculus
Inferior collicu
ulus Optic radiation
Superior cerebellar peduncle
Dentate fascia
Subiculum
Spinal tract of Presubiculum
trigeminal nervee
Calcarine sulcus
Posterior horn of Decussation of inferior
laterral ventricle cerebellar pe
eduncle
Emboliform
m nucleus
Dentate nucleus
D
Lamina
a albae
Lateral sulcus
Corona rad
diata
Trrigone of
Posterior limb of latteral ventricle
internal capsulee
Claustrum
m
Ca
alcarine sulcus
Amygdala Collateral sulcus
Hippocampus
Inferior
ior horn of Dentate
lateral ventricle fascia
Subthalamic nucleus
Splenium
m of corpus
Anterior limb of callosum
m
internal capsuule
Pulvinar
Medial medullary lamina
of globus pallidus Ce
entromedian
nucleus
Ansa lenticcularis
Inferior cerebellar
peeduncle
Pyramidal decussation
Central
sulcuss
Body of lateral
ventricle
Centrum
semiov
vale
Head of caudate
nucleus
Great longitudinal fissure
Corpu
us callosum
Anterior horn of
la
ateral ventricle
Thalamostriate
vein Ca
avum septi pellucidi
Ve
ein of septum
Thalamus pe
ellucidum
Corpu
us callosum
Ta
ail of caudate
nucleus
Choroid plexus of
lateral ventricle
mn of fornix
Colum
Genu of corpus callosum
Interventricular fora
amen
(of Monro)
Vein of septum pellucidum
Puta
amen T
Thalamostriate vein
Choroidal vein
C
Globus pallidus Ve
entrolateral thalamic nuclei
Me
edial thalamic nuclei
Claustru
um
P
Pulvinar
Internal capsule
Crrus of fornix
Splenium oof
corpus calllosum
Glomus of choroid
d plexus
Ansa lenticularis
Perforating fibre
es of internal capsule
Third ventricle
Medial part off globus pallidus
Column of fornix
Laterral geniculate body
Anterior commissure
e
Subthalamic nucleus
s
Medial lemniscuss
Red nuclleus
H
Hippocampus
Medial longitudinal fas
sciculus
De
entate fascia
Optic rece
ess
Optic tract
Infundibulum
Uncuss Mammillary body
M
Dentate fascia
a
Nu
ucleus of trochlear nerve and
medial longitudinal fasciculus
Limbus Giacomini
Substantia nigra IInferior
f i colliculus
Trigeminal
nal nerve Pyramidal tract
tra
Medial le
emniscus
Laterral lemniscus
Vestibulomesencepha
alic tract
Centrral tegmental tract
Fourth ventric
cle
Superior cerebellar peduncle
Uvula
Dentate nucleus
Vermis
ermis
Medial
lemniscus
Trapezoid body Pyramidal tract
trac
Superio
or olive
Floc
cculus
Sp
pinal tract of trigeminal nerve
Vestibular nucleii
Inferior cerebellar peduncle
Nodulus
Uvu
ula Dentate nucleus
Pyra
amid
Centrum semiovale
Olfactory sulcus
Olfactory tract
Anterior commiss
sure Lateral sulcus
Third ventrricle C
Claustrum
Globus pallidus
Inffundibulum
Amygdala
Uncus
Supraoptic
ic commissure Optic
Substantia
tract innominata
Subthalamic nuccleus
Inferior ho
orn of lateral ventricle
Cerebra
al peduncle
Hippocampus
Mammillary body Hi
Hippocampal
l
sulcus
Precentral gyrus
gyr
Corpus callosum
Intternal capsule
Forrnix
Subthalamic nucleus
Red nu
ucleus
Optic tract
Pyramidal tract
Interpeduncular fossa
Postcentral gyrus
Cingu
ulate gyrus
Corpus callosum
P
Pulvinar
Superior co
olliculus
Dentate
e fascia
Subiculum
Spinal tract of trigeminal nerve
e Presubiculum
Med
dial lemniscus Flocculus
Calcarine sulcus
Posterior horn of Decussation of in
nferior
lateral ventricle cerebellar pedun
ncle
Emboliform nucleus
n
De
entate nucleus
Lamiina albae
Lateral sulcus
Corona ra
adiata
Putamen
Posterior horn of
Lateral geniculate bodyy lateral ventricle
Claustrum
Calcarine sulcus
Amygdala Collateral sulcus
Hippocampus
Dentate
Inferior horn of fascia
lateral ventricle
Denta
ate nucleus
Fl
Flocculus
l
Decussation of superior
cerebellar pe
eduncle
Medial longitudinal fasciculus
Medial lemniscus Graccile nucleus
Cune
eate nucleus
Pyramidal
id l decussation
d ti
Central
sulcuss
Body of lateral
ventricle
Centrum
semiovvale
Head of caudate
nucleus
Great lo
ongitudinal fissure
Corpus callosum
Anterior horn of
la
ateral ventricle
Thalamostriate
e
veinn Cavum septi pellucidi
Ve
ein of septum
Thalamus pe
ellucidum
Corpu
us callosum
Tail of caudate
nucleus
Choroid plexus of
lateral ventricle
Colum
mn of fornix
Genu
u of corpus callosum
Interventricular forramen
(of Monro)
Vein of septum pellucidum
Thalamostriate vein
T
Putamen
Choroidal vein
C
Globus pallidu
us Ve
entrolateral thalamic nuclei
Me
edial thalamic nuclei
Claustrrum
P
Pulvinar
Internal capsule
Crus of fornix
Splenium of
o
corpus calllosum
Glomus of choroid
d plexus
Optic recess
Optic tract
O
Infundibulum
Uncus
s Mammillary body
Dentate fascia
a Nuucleus of trochlear nerve and
Limbus Gia
acomini medial longitudinal fasciculus
Substantia nigra IInferior
f i colliculus
Uvula
a
Vermis
ermis Dentate nucleus
Medial lemniscus
Trapezoid body Pyramidal tracct
Superior olive
Floccculus
Sp
pinal tract of trigeminal nerve
Vestibular nuclei
Inferior cerebellar peduncle
Nodulus
Uvula Dentate nucleus
Pyramid
Centrum semiovale
Olfactory sulcus
Olfactory tract
Corpus
p callosum
Cavum septi pellucidi
Body of caudate nucleus
Anterior lim
mb of
internal cap
psule
Anterior horn off
lateral ventricle
e
Extternal capsule
Vein of septum P
Putamen
pellucidum
Third venttricle C
Claustrum
Globus pallidus
Infundibulum
Amygdala
Uncus
Supraoptic
ptic commissure Optic
tract Substantia
innominata
Optic tra
act Ansa lenticularis
A
Subthalamic nuccleus
Inferior ho
orn of lateral ventricle
Cerebra
al peduncle
Hippocampus
Mammillary body
Hippocampal
sulcus
Precentral gyrus
Corpus
s callosum
Intternal capsule
Forrnix
Subthalamic nu
ucleus
Red nu
ucleus
Optic tract
Pyramidal tract
IInterpeduncular
t d l fossa
f
Postcentral gyrus
Cingu
ulate gyrus
Corpus callosum
P
Pulvinar
Superior colliculus
Dentate
e fascia
Subiculum
Spinal tract of trigeminal nerve
e Presubiculum
Media
al lemniscus Flocculus
Calcarine sulcus
Po
osterior horn of Decussation of inferior
lateral ventricle cerebellar pedunccle
Emboliform nucleus
n
De
entate nucleus
Lam
mina albae
Lateral sulcus
Corona rad
diata
Posterior limb off
internal capsulee Trrigone of
lateral ventricle
Putamen
Posterior horn of
Lateral geniculate bodyy lateral ventricle
Claustrum
m
Caalcarine sulcus
Amygdala Collatera
al sulcus
Hippocampus
Inferior
or horn of Dentate
lateral ventricle fascia
Subthalam
mic nucleus
Anterior limb of Splenium of corpus callosum
internal capsuule
Pulvina
ar
Medial medullary laminaa
of globus palliduss Ce
entromedian nucleus
Ansa lentic
cularis
Infferior cerebellar peduncle
Cerebellar hemisphere
C
Optic tract
Cerebral peduncle
Denta
ate nucleus
Flocculus
Cavum septi
epti pellucidi Anterior thalamic nuclei
Lateral ventricle Medullary sstria of thalamus
Cavum vvergae
Genu of corpus Splenium of corpus callosum
callosum
Poste
erior commissure
Nucleeus of oculomotor nerve
Anterior commissure Cereebral aqueduct
Third ventriicle Commissure of inferior colliculus
Media
al lemniscus
Grac
cile nucleus
Cune
eate nucleus
Pyramidal
id l d
decussation
ti
Central
sulcuss
Body of lateral
ventricle
Centrrum
semiov
vale
Head of caudate
e nucleus
Great lon
ngitudinal fissure
Corpu
us callosum
Annterior horn of
latteral ventricle
Thalamostriate vein
n
Ca
avum septi pellucidi
Ve
ein of septum
Thalamus pe
ellucidum
Corpuss callosum
Tail of cau
udate nucleus
Choroid plexus of
lateral ventricle
Column of fornix
Genu of ccorpus callosum
Interventricular fo
oramen
(of Monro)
Ve
ein of septum pellucidum
Thalamostriate vein
T
Pu
utamen
Choroidal vein
C
Globus pallidu
us Ve
entrolateral thalamic nuclei
Me
edial thalamic nuclei
Claustrum
P
Pulvinar
Internal capsule
Crus of fornix
us
Tail of caudate nucleu Intern
nal cerebral vein
Cavum ve
ergae
Splenium of
corpus callossum
Glomus of choro
oid plexus
Optic rece
ess
Op
ptic tract
Infundibulum
Uncuss Mammillary body
Dentate fascia
a Nu
ucleus of trochlear nerve and
me
edial longitudinal fasciculus
Limbus Giiacomini
Substantia nigra Inferior col
colliculus
Pyramidal tract
Trigeminall nerve
Medial lemniscus
Lateral lemniscus
Vestibulomesencepha
alic tract
Centrral tegmental tract
Fourth ventric
cle
Superior cerebellar peduncle
S
Uvula
a
Vermis
ermis Dentate nucleus
Medial lemniscus
Trapezoid body Pyramidal trract
Superrior olive
Floccculus
Sp
pinal tract of trigeminal nerve
Vestibular nucleii
Inferior cerebellar peduncle
Nodulus
Uvulaa Dentate nucleus
Pyram
mid
Centrum semiovale
C
Olfactory sulcus
O
Olfactory tract
Cavum septi
p Corpus callosum
pellucidi Body of caudate
e nucleus
Anterior lim
mb of
internal capsule
Anterior horn of
lateral ventricle
Extternal capsule
Vein of septum P
Putamen
pellucidum
Lateral sulcus
Anterior commiss
sure
Third ventricle C
Claustrum
Glo
obus pallidus
In
nfundibulum
Amygdala
Uncus
Supraoptic
ptic commissure Optic
Substantia
tract
innominata
Optic tra
act Ansa lenticularis
A
Subthalamic nuc
cleus
Inferior horn of lateral ventricle
Cerebrral peduncle
Hippocampus
Mammillary body
Hippocampal
sulcus
Precentral gyrus
gyr
Corpus ca
allosum
Intternal capsule
Forrnix
Subthalamic nuccleus
Red nu
ucleus
Optic tract
Pyramidal tract
IInterpeduncular
d l fossa
f
Postcentral gyrus
gy
Cingu
ulate gyrus
Corpus callosum
P
Pulvinar
Superior collliculus
ulus
Inferior collicu Optic radiation
Superior cerebellar peduncle
Dentate
e fascia
Subiculum
Spinal tract of trigeminal nerve Presubiculum
Pyramid IInferior
f i olive
li
Calcarine sulcus
s lc s
Posterior horn of Decussation of infe
erior
lateral ventricle cerebellar peduncle
e
Emboliform nu
ucleus
De
entate nucleus
Lam
mina albae
Lateral sulcus
Corona ra
adiata
Putamen
Posterior horn of
Lateral geniculate bodyy lateral ventricle
Claustrum
m
Caalcarine sulcus
Amygdala Collateral sulcus
Hippocampus
Dentate
Inferior horn of fascia
lateral ventricle
Subthalamic nucleus
Splenium
m of corpus callosum
Anterior limb of
internal capsuule
Pulvinar
Medial medullary lamina
of globus pallidus
Ce
entromedian nucleus
Ansa lentic
cularis
In
nferior cerebellar peduncle
Cerebral peduncle
Denta
ate nucleus
Flocculus
Cavum septi
epti pellucidi Anterior thalamic nuclei
Lateral ventricle Medullary stria of thalamus
Cavum vergae
v
Genu of corpus Splenium of corpus callosum
callosum
Posterior commissure
Nucleeus of oculomotor nerve
Anterior commissure Cereebral aqueduct
Third ventriicle Commissure of inferior colliculus
Media
al lemniscus
Graccile nucleus
Cune
eate nucleus
Pyramidal
id l decussation
d ti
Central
sulcuss
Body of lateral
ventricle
Centrum
semiovvale
Head of caudate
nucleus
Great lo
ongitudinal fissure
Corpu
us callosum
Anterior horn of
la
ateral ventricle
Thalamostriate
e
veinn
Cavum septi pellucidi
C
Ve
ein of septum
pe
ellucidum
Thalamus
Corpu
us callosum
Ta
ail of caudate
nucleus
Choroid plexus of
lateral ventricle
Colum
mn of fornix
Genu of
o corpus callosum
Interventricular forramen
(of Monro)
Vein of septum pellucidum
T
Thalamostriate vein
Puttamen
C
Choroidal vein
Globus pallidu
us Ve
entrolateral thalamic nuclei
Me
edial thalamic nuclei
Claustrrum
P
Pulvinar
Internal capsule
Crrus of fornix
Cavum vvergae
Splenium of
corpus callosum
Glomus of choroid
d plexus
Optic reccess
O
Optic tract
Infundibulum
Uncuss Mammillary body
M
Pyramidal tract
Trigeminal
nal nerve
Medial le
emniscus
Lateral lemniscus
Vestibulomesencepha
alic tract
Centtral tegmental tract
Fourth ventric
cle
S
Superior cerebellar
peduncle
Uvula
a
Dentate
e nucleus
Pyramis vermis
ermis
Medial lemniscus
Trapezoid body Pyramidal tract
Superiorr olive
Flo
occulus
Sp
pinal tract of trigeminal nerve
Vestibular nuclei
Nodulus
Pyrramid
Centrum semiovale
Olfactory sulcus
Olfactory tract
Third ventrricle C
Claustrum
Gllobus pallidus
Inffundibulum
Amygdala
Uncus
Supraoptic commissure
i Optic Substantia
tract innominata
Subthalamic nucleus
Inferior horn
h of lateral ventricle
Cerebral peduncle
Hippocampus
Mammillary
ammillary body Hi
Hippocampal
l
sulcus
Precentral gyru
us
Corpus callosum
Intternal capsule
Forrnix
Subthalamic nu
ucleus
Red nu
ucleus
Optic tract
Pyramidal tract
Interpeduncular fossa
Postcentral gyrus
Cing
gulate gyrus
Corpus ca
allosum
P
Pulvinar
Superior colliculus
Superior cerebellar
peduncle
Dentate
e fascia
Subiculum
Spinal tract of
Presubiculum
trigeminal nerve e
Med
dial lemniscus Flocculus
P
Pyramid
id Inferior olive
Calcarine sulcus
osterior horn of
Po Decussation of in
nferior
la
ateral ventricle cerebellar pedunccle
Emboliform nu
ucleus
De
entate nucleus
Lamina albae
Lateral sulcus
Corona rad
diata
Posterior limb off Trrigone of
internal capsulee latteral ventricle
m
Claustrum
Caalcarine sulcus
Am
mygdala Collaterral sulcus
Hippocampus
Dentate
Inferior horn of fascia
lateral ventricle
Subthalamicc nucleus
Splenium
m of corpus
callosum
m
Anterior limb of
internal capsule
Pulvinar
Medial medullary laminaa
of globus palliduss Ce
entromedian
nu
ucleus
Ansa lentic
cularis
In
nferior cerebellar
pe
eduncle
Cerebellar
C
Optic tract h
hemisphere
Cerebral peduncle
Denta
ate nucleus
Flocculus
Cavum septi
epti pellucidi Anterior thalamic nuclei
Lateral venntricle Medullary stria
s of thalamus
Cavum vergae
v
Genu of corpus
Splenium of corpus callosum
callosum
Posterior commissure
Nucle
eus of oculomotor nerve
Anterior commissure Cereebral aqueduct
Third ventriicle Commmissure of inferior colliculus
Decussation of su
uperior
cerebellar pe
eduncle
Media al lemniscus
Gracile nucleus
Cune
eate nucleus
Pyramidal
id l d
decussation
i
Centrall
sulcus
s
Body of lateral
ventricle
Centrrum
semiov
vale
Head of caudate
nucleus
Great lo
ongitudinal fissure
Corp
pus callosum
A
Anterior horn of
la
ateral ventricle
Thalamostriate
e
veinn Cavum septi pellucidi
Ve
ein of septum
pe
ellucidum
Thalamus
Corp
pus callosum
Tail of caudate
nucleus
Choroid plexus of
lateral ventricle
Co
olumn of fornix
Genu off corpus callosum
Interventricular forramen
(of Monro)
Vein of septum pellucidum
V
Thalamostriate vein
T
Puttamen
C
Choroidal vein
us
Globus pallidu Ventrolateral thalamic nuclei
Me
edial thalamic nuclei
Claustrrum
P
Pulvinar
Internal capsule
Crrus of fornix
Cavum vergae
d plexus
Glomus of choroid
Optic re
ecess
O
Optic tract
Infundibulum
Uncus Mammillary body
Dentate fascia
a Nu
ucleus of trochlear nerve and
medial longitudinal fasciculus
Limbus Giaccomini
Substantia
t ti nigra
i Inferior colliculus
Inferio
Trigeminal
al nerve Pyramidal tract
trac
Medial le
emniscus
Laterral lemniscus
Vestibulomesencephalic tract
Centrral tegmental tract
Fourth ventric
cle
Superior cerebellar peduncle
Uvula
a
Dentate nucleus
Pyramis vermis
Medial lemniscus
Trapezoid body Pyramidal trac
ct
Superior olive
Floc
cculus
Sppinal tract of
Vestibular nuclei trigeminal nerve
Inferior cerebellar
peduncle
Nodulus
Uvula Dentate nucleus
Pyra
amid
Centrum semiovale
Olfactory sulcus
Olfactory tract
Third ventrricle C
Claustrum
Gllobus pallidus
Inffundibulum
Amygdala
Uncus
Optic
Supraoptic commissure Substantia
tract
innominata
Subthalamic nuccleus
Inferior horn of lateral ventricle
Cerebral peduncle
Hippocampus
Mammillary body
Hippocampal
sulcus
Precentral gyrus
gyru
Corpus callosum
Intternal capsule
Forrnix
Subthalamic nu
ucleus
Red nu
ucleus
Optic tract
Pyramidal tract
Interpeduncular fossa
Postcentral gyrus
Cing
gulate gyrus
Corpus callosum
P
Pulvinar
Superior collliculus
Dentatte fascia
Subiculum
m
Spinal tract of
Presubiculum
m
trigeminal nerve e
Calcarine sulcus
Posterior horn of Decussation of in
nferior
la
ateral ventricle cerebellar pedun
ncle
Emboliform nu
ucleus
De
entate nucleus
Lamina albae
Lateral sulcus
Corona radiata
Trrigone of
Posterior limb of latteral ventricle
internal capsulee
Ca
alcarine sulcus
Amygdala Collatera
al sulcus
Hippocampus
Dentate
Inferior horn of fascia
lateral ventricle
Subthalamic nucleus
Splenium
m of corpus callosum
Anterior limb of
internal capsuule
Pulvin
nar
Medial medullary lamina
of globus pallidus Ce
entromedian nucleus
Ansa lenticularis
In
nferior cerebellar peduncle
Cerebellar hemisphere
Optic tract
Cerebral peduncle
Dentate nucleus
Denta
Flocculus
Decussation of superior
cerebellar peduncle
dial lemniscus
Med
Graccile nucleus
Cunea ate nucleus
Pyramidal decussation
261
262 SUBJ EC T IN D E X
Fetal brain (Continued) Glossopharyngeal nerve, 73f, 103f, 109f Inferior frontal sulcus, 9, 13, 17
stages of development, 37t Gracile nucleus Inferior olivary nucleus, 130f
transient structures, 35–38 fetus (coronal), 131f Inferior olive
Fetal sulcation milestones, 17t fetus (sagittal), 60f, 134f, 151f fetus (axial), 103f
Fimbria of hippocampus postnatal (sagittal), 179f, 196f, 212f, fetus (coronal), 56f, 73f, 91f, 146f, 223f
fetus (axial), 66f, 99f, 118f 228f, 244f, 260f fetus (sagittal), 60f, 76f, 77f, 94f, 113f
fetus (coronal), 55f, 88f, 147f Great cerebral vein, 118f postnatal (coronal), 174f, 191f, 207f,
fetus (sagittal), 93f Great cerebral vein (of Galen), 76f 239f, 255f
First year of life. See Postnatal brain Great longitudinal fissure
fi Inferior sagittal sinus, 8f
FLAIR image, 155f fetus (axial), 96f, 114f Inferior surface, 27–30
Flocculus postnatal (axial), 181f, 198f, 214f, 230f, Inferior temporal gyrus, 10f, 11f, 26f
fetus (axial), 103f, 124f 246f Inferior temporal sulcus, 10f, 13, 17, 26f
fetus (coronal), 73f, 109f, 130f, 145f Gyrus brevi, 9, 14f Infratentorial brain, 155f
fetus (sagittal), 58f, 75f, 112f, 149f Gyrus longus, 9, 14f Infundibular nucleus, 49f, 66f
postnatal (axial), 169f, 186f, 202f, 218f, Gyrus rectus, 101f, 121f Infundibular recess, 134f
234f, 250f Infundibulum
postnatal (coronal), 174f, 191f, 207f, fetus (axial), 83f
223f, 239f, 255f H fetus (coronal), 143f
postnatal (sagittal), 178f, 195f, 211f, Habenula postnatal (axial), 165f, 184f, 188f, 200f,
227f, 243f, 259f fetus (axial), 46f, 64f, 80f, 100f, 118f, 216f, 232f, 248f
Fornix. See also Column of fornix; Crus of 139f postnatal (coronal), 171f, 204f, 220f,
the fornix fetus (coronal), 88f 236f, 252f
fetus (axial), 63f Habenulo-interpeduncular tract Insula, 9, 14f, 24f, 25f, 26f
fetus (coronal), 70f, 86f, 128f, 144f fetus (axial), 47f, 48f, 81f, 119f, 120f Insular cortex
medial surface, 32f fetus (coronal), 55f, 88f, 129f, 145f fetus (axial), 99f, 117f, 138f
postnatal (axial), 161f, 162f, 163f, 164f, Hippocampal sulcus fetus (coronal), 70f, 106f, 127f
181f, 182f, 183f, 189f, 198f, 199f, fetus (axial), 83f, 121f postnatal (axial), 189f
214f, 230f, 246f fetus (coronal), 221f postnatal (coronal), 172f, 221f, 237f,
postnatal (coronal), 172f, 173f, 190f, fetus (sagittal), 111f 253f
205f, 206f, 221f, 222f, 237f, 238f, postnatal (axial), 189f Intermediate zone, 36, 37f, 38t
253f, 254f postnatal (coronal), 172f, 205f, 237f, Internal capsule, 37f
Fourth ventricle 253f fetus (axial), 44f, 62f, 79f, 81f, 99f, 117f,
fetus (axial), 50f, 67f, 103f, 122f Hippocampus 119f, 136f, 137f, 138f, 139f
fetus (coronal), 56f, 73f, 90f, 130f, 147f fetus (axial), 46f, 65f, 81f, 82f, 83f, 100f, fetus (coronal), 52f, 54f, 69f, 70f, 72f,
fetus (sagittal), 58f, 59f, 75f, 76f, 77f, 101f, 119f, 121f, 140f 85f, 105f, 106f, 126f
94f, 95f, 113f, 134f, 151f fetus (coronal), 55f, 72f, 87f, 90f, 107f, fetus (sagittal), 57f, 74f, 110f, 111f, 148f
postnatal (axial), 167f, 185f, 201f, 217f, 108f, 128f postnatal (axial), 161f, 162f, 163f, 164f,
233f, 249f fetus (sagittal), 57f, 110f, 148f 181f, 182f, 183f, 188f, 198f, 199f,
Funiculus anterior, 131f postnatal (axial), 164f, 165f, 183f, 184f, 214f, 215f, 230f, 231f, 246f, 247f
189f, 200f, 216f, 232f, 248f postnatal (coronal), 171f, 173f, 190f,
postnatal (coronal), 172f, 194f, 205f, 194f, 204f, 206f, 220f, 222f, 236f,
G 221f, 237f, 253f 238f, 252f, 254f
Gangliothalamic body, 81f postnatal (sagittal), 177f, 210f, 226f, postnatal (sagittal), 177f, 178f, 195f,
Garel, Catherine, 15 242f, 258f 210f, 211f, 226f, 227f, 242f, 243f,
Geniculate body, 120f Holoprosencephaly, 15 258f, 259f
Gennari’s band, 119f Horizontal fissure, 131f, 141f Internal cerebral vein
Germinal matrix, 35, 36, 37f Hypoglossal nerve, 91f, 109f, 151f fetus (axial), 116f, 117f, 137f, 139f
fetus (axial), 48f, 51f, 52f, 53f, 54f, Hypothalamus, 70f, 86f, 106f, 120f, 121f fetus (coronal), 88f, 129f
62f, 64f, 66f, 78f, 79f, 81f, 82f, fetus (sagittal), 76f
96f, 97f, 98f, 99f, 100f, 101f, postnatal (axial), 162f, 182f, 199f, 215f,
114f, 115f, 116f, 119f, 120f, 136f, I 231f, 247f
137f, 138f, 139f In utero imaging of fetus, 4–5 Interpeduncular fossa
fetus (coronal), 69f, 72f, 85f, 86f, 87f, Indusium griseum, 90f, 97f, 115f fetus (coronal), 55f
89f, 104f, 105f, 106f, 107f, 125f, Infant. See Postnatal brain postnatal (coronal), 173f, 190f, 206f,
126f, 142f, 143f, 144f Inferior cerebellar peduncle 222f, 238f, 254f
fetus (sagittal), 58f, 75f, 92f, 93f, 94f, fetus (axial), 67f, 102f, 122f, 123f, 124f, Interventricular foramen, 117f, 127f, 138f
110f, 112f, 132f, 148f, 149f, 150f 141f Interventricular foramen (of Monro)
Gestational age. See Fetal brain fetus (coronal), 109f, 130f, 146f, 147f fetus (axial), 63f, 98f
Gliosis, 155f fetus (sagittal), 58f, 149f, 150f fetus (sagittal), 76f
Globose nucleus, 91f, 102f postnatal (axial), 168f, 169f, 186f, 202f, postnatal (axial), 162f, 182f, 199f, 215f,
Globus pallidus 218f, 234f, 250f 231f, 247f
fetus (axial), 46f, 47f, 63f, 65f, 80f, 99f, postnatal (coronal), 208f iuMR, 2
100f, 117f, 118f, 119f, 120f, 139f postnatal (sagittal), 175f, 195f, 211f,
fetus (coronal), 53f, 70f, 71f, 86f, 106f, 227f, 243f, 259f
127f, 128f, 143f, 144f Inferior colliculus J
fetus (sagittal), 58f, 74f, 93f, 110f, 132f, fetus (axial), 48f, 66f, 101f, 140f Juxtarestiform body, 123f
133f, 148f, 149f fetus (coronal), 56f, 73f, 90f, 108f, 145f,
postnatal (axial), 162f, 163f, 164f, 182f, 146f, 147f
183f, 188f, 189, 189f, 199f, 215f, fetus (sagittal), 60f, 94f, 112f L
231f, 247f postnatal (axial), 165f, 184f, 200f, 216f, Lamina albae
postnatal (coronal), 171f, 172f, 204f, 205f, 232f, 248f postnatal (coronal), 192f, 208f, 224f,
220f, 221f, 236f, 237f, 252f, 253f postnatal (coronal), 174f, 191f, 207f, 240f, 256f
postnatal (sagittal), 178f, 195f, 211f, 223f, 239f, 255f postnatal (sagittal), 175f
227f, 243f, 259f Inferior frontal gyrus, 10f, 26f Lamina terminalis, 65f, 119f
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Orbital sulcus, 30f Precentral sulcus, 10f, 21f, 22f, 26f Sagittal section, fetal brain (Continued)
Overview of atlas, 2 Precuneus, 11f, 33f, 34f 25–26 weeks, 92–95
Presubiculum, 174f, 191f, 207f, 223f, 239f, 28–29 weeks, 110–113
255f 32–33 weeks, 132–134
P Primary germinal matrix, 35, 36 36–37 weeks, 148–151
Parieto-occipital sulcus, 9, 10f, 11f Pulvinar Sagittal section, postnatal brain
fetus (sagittal), 60f, 111f, 133f fetus (axial), 46f, 64f, 80f, 81f, 99f, 100f, 0–1 month, 175–179
medial surface, 32f, 33f, 34f 117f, 118f, 119f, 139f 3–4 months, 195–196
superior surface, 20f, 21f, 22f fetus (coronal), 147f 6 months, 209–212
Pars marginalis, 16f fetus (sagittal), 59f, 93f, 110f, 111f, 9 months, 225–228
Pars marginalis of cingulate sulcus, 11f, 132f, 133f 12 months, 241–244
33f, 34f postnatal (axial), 162f, 163f, 182f, 199f, 18 months, 257–260
Pars opercularis, 13f 215f, 231f, 247f Secondary germinal matrix, 35, 36
Pars orbitalis, 13f postnatal (coronal), 174f, 191f, 207f, Sectional anatomy. See Fetal brain;
Pars triangularis, 13f 223f, 239f, 255f Postnatal brain
Pedunculus cerebellaris inferior, 112f postnatal (sagittal), 178f, 195f, 211f, Septum pellucidum. See also Vein of
Perforating fibres
fi 227f, 243f, 259f septum pellucidum
fetus (coronal), 128f Putamen, 37f fetus (axial), 44f, 63f, 97f, 98f, 116f
fetus (sagittal), 132f, 133f, 149f fetus (axial), 44f, 45f, 47f, 63f, 65f, 80f, fetus (coronal), 143f
postnatal (axial), 189f 100f, 116f, 120f, 137f, 139f fetus (sagittal), 112f
postnatal (coronal), 172f, 205f, 221f, fetus (coronal), 52f, 53f, 69f, 70f, 85f, Somatosensory radiation, 135f, 148f
237f, 253f 105f, 126f, 143f, 144f STF1, 36
Pia meter, 8f fetus (sagittal), 57f, 58f, 74f, 93f, 110f, STF2, 36
Pineal body, 146f 111f, 148f, 149f STF3, 36
Pineal gland postnatal (axial), 162f, 182f, 188f, 199f, STF4, 36
fetus (axial), 46f, 64f, 118f 215f, 231f, 247f STF5, 36
fetus (sagittal), 77f, 95f, 134f, 151f postnatal (coronal), 171f, 194f, 204f, STF6, 36
medial surface, 32f 220f, 236f, 252f Stratified
fi transitional field (STF), 36
pmMR, 2 postnatal (sagittal), 177f, 210f, 226f, Striatal matrix, 35
Pons, 11f 242f, 258f Subarachnoid space, 8f
fetus (axial), 50f, 67f, 122f Pyramid Subcentral gyrus, 13f
fetus (coronal), 55f, 89f, 108f, 129f fetus (axial), 102f, 103f, 141f Subcommissural organ, 81f, 119f
fetus (sagittal), 59f, 113f, 134f fetus (coronal), 56f, 73f, 130f Subependymal vein, 115f, 144f
inferior surface, 28f, 29f, 30f postnatal (axial), 169f, 186f, 202f, 218f, Subiculum, 174f, 191f, 207f, 223f, 239f,
medial surface, 34f 234f, 250f 255f
Postcentral gyrus, 10f, 16f postnatal (coronal), 174f, 191f, 207f, Subplate, 37f, 38, 38t
lateral surface, 25f, 26f 223f, 239f, 255f Substantia innominata
postnatal (coronal), 174f, 191f, 207f, Pyramidal decussation postnatal (axial), 188f
223f, 239f fetus (coronal), 146f postnatal (coronal), 171f, 204f
superior surface, 21f, 22f fetus (sagittal), 134f, 151f Substantia innominata
Postcentral sulcus, 10f, 16f postnatal (sagittal), 179f, 196f, 212f, fetus (axial), 120f
fetus (axial), 114f, 135f 228f, 244f, 260f fetus (coronal), 127f, 143f
lateral surface, 26f Pyramidal tract fetus (sagittal), 111f
superior surface, 21f, 22f fetus (axial), 50f, 84f postnatal (coronal), 220f, 236f, 252f
Posterior ascending ramus, 12f fetus (coronal), 55f, 89f, 90f, 108f, 129f Substantia nigra
Posterior cerebral artery, 83f, 128f fetus (sagittal), 59f, 60f, 76f, 77f, 94f, fetus (axial), 49f, 66f, 83f, 101f
Posterior commissure 95f, 113f fetus (coronal), 55f, 88f
fetus (axial), 119f postnatal (axial), 166f, 167f, 168f, 169f, fetus (sagittal), 59f, 111f
fetus (coronal), 129f, 145f 185f, 186f, 201f, 202f, 217f, 218f, postnatal (axial), 165f, 184f, 200f, 216f,
fetus (sagittal), 77f, 113f 233f, 234f, 249f, 250f 232f, 248f
postnatal (sagittal), 179f, 196f, 212f, postnatal (coronal), 173f, 190f, 206f, Subthalamic nucleus
228f, 244f, 260f 222f, 254f fetus (axial), 48f, 65f, 119f, 120f
Posterior descending ramus, 12f Pyramis vermis, 233f, 249f fetus (coronal), 54f, 71f, 72f, 87f, 107f,
Posterior horizontal ramus, 12f 128f
Posterior perforated substance, 134f fetus (sagittal), 59f, 75f, 111f, 133f, 149f
Posterior ramus, 9 Q postnatal (axial), 164f, 183f, 189f
Posterior spinocerebellar tracts, 131f Quadrigeminal plate, 47f, 65f, 76f, 150f postnatal (coronal), 172f, 173f, 190f,
Postmortem fetal tissue sections, 2 205f, 206f, 221f, 222f, 237f, 238f,
Postmortem MR imaging of fetus, 2–4 253f, 254f
Postnatal brain, 153–260 R postnatal (sagittal), 178f, 195f, 211f,
axial section. See Axial section, Red nucleus 227f, 243f, 259f
postnatal brain fetus (axial), 48f, 120f, 121f Subventricular zone, 35, 37f, 38t
coronal section. See Coronal section, fetus (coronal), 55f, 88f Sulcus hypothalamicus, 106f
postnatal brain fetus (sagittal), 60f, 76f, 112f, 113f, 150f Sulcus visualization, 17t
myelination, 153–154, 157t postnatal (axial), 164f, 183f Superficial
fi cerebral vein, 8f
overview, 153–157 postnatal (coronal), 173f, 190f, 206f, Superior cerebellar peduncle
sagittal section. See Sagittal section, 222f, 238f, 254f fetus (axial), 49f, 66f, 122f, 140f
postnatal brain Rhinencephalic cavity, 52f, 60f fetus (coronal), 56f, 130f, 145f, 146f,
Postnatal MR imaging, 5 147f
Precentral gyrus, 10f, 13f, 16f postnatal (axial), 164f, 166f, 167f, 183f,
lateral surface, 25f, 26f S 185f, 201f, 217f, 233f, 249f
postnatal (coronal), 173f, 190f, 206f, Sagittal section, fetal brain postnatal (coronal), 173f, 174f, 190f,
222f, 238f, 254f 19–20 weeks, 57–60 191f, 206f, 207f, 222f, 223f, 238f,
superior surface, 21f, 22f 22–23 weeks, 74–77 239f, 254f, 255f
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