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Cagampan Date of Lecture: January 30, 2012 Transcriptionist: Gluttonoids Editor: Gluttonoids Pages: 4
Congenital hydroureter reflect some neurogenic defect in the inndervation of the ureteral musculature Makes ureter more prone to kinking and obstruction
URETERS
I. CONGENITAL ANOMALIES (2%-3%)
Main Significance: may contribute to obstruction
5. Megaloureter Massive enlargement of the ureter May be due to a functional defect of ereteral mmuscle My also occur in severe cases of obstruction
Most common cause of hydronephrosis in infants and children; In infants- more common in boys, usually on the left ureter and more commonly unilteral In adults, more common among women and most often unilateral Abnormal organization of smooth muscle bundles excess collagen deposition between smooth muscle bundles ureteropelvic junction becomes small obstruction hydronephrosis of the involved kidney
appear as protrusions or undulations on the surface of the ureteral mucosa and produce a fine granular mucosal surface b. Ureteritis cystica small cysts on the surface of the ureter
SY 2011-2012
composed of loose vascularized connective tissue mass beneath the mucosa may also appear in the bladder, urethra, and renal pelvis
2. Leiomyoma - another
very common benign tumor of the ureter 3. Urothelial carcinoma
th
pouchlike evangination of the bladder wall <1 cm 10 cm Congenital: focal failure of development of normal musculature Urinary tract obstruction during fetal development Acquired: Seen with prostatic enlargement Obstruction to urine outflow and muscle thickening in urinary bladder intravesical pressure formation of outpouchings or divertucula Clinical significance:
Sites of urinary stasis infection Impinge on the ureter & cause vesivulo-ureteral reflux May give rise to cancers
2. Exstrophy
Anterior wall of the abdomen fails to develop bladder communicates directly with the surface of the body or it lies as an open sac Exposed mucosa undergoes metaplasia More prone to infection Increased risk of developing adenocarcinoma Amenable to surgeical correction
Leads to
hydroureter/hydronephro sis and sometime pyelonephritis Unilateral obstruction results from proximal causes Bilateral obstruction arises from distal causes (e.g. nodular hyperplasia of the prostate)
Sclerosing
Retroperitoneal Fibrosis
Forms of Cystitis:
URINARY BLADDER
I. CONGENITAL ANOMALIES 1. Diverticula
Non-specific acute (&chronic) inflammation Types: a. Hemorrhagic cystitis after radiation treatment or antitumor treatment b. Suppurative cystitis c. Ulcerative cystitis 2. Chronic Cystitis Morphology: Predominance of chronic inflammatory cells Heaping up of the epithelium & granular surface Fibrous thickening of the muscularis propria bladder wall become less elastic Morphologic variants: a. Follicular cystitis ~ lymphoid follicles within the bladder mucosa and wall ~ not necessarily associated with infection b. Eosinophilic cystitis ~ submucosal eosinophils, fibrosis, occasionally giant cells ~ nonspecific subacute inflamamtion
Fibrosis may ensue, leading to a contracted bladder Unknown etiology Early Phase(nonclassic, non-ulcerative) ~ recent submucosal haemorrhages
~ Inflammation & granulation tissue in mucosa, lamina propria & muscularis ~ Mast cells may be prominent
b.
Malacoplakia Vesical inflammatory reaction 3 cm 4cm slightly raised, soft, yellow, mucosal plaques Large foamy macrophages with occ. Multinucleated giant cells, interspersed with lymphocytes Michaelis-Gutmannbodies laminated mineralized concretions (calcium) in macrophages and between cells
a. Frequency urination
every 15 to 20 minutes b. Lower abdominal Pain over the bladder region or in the suprapubic region c. Dysuria pain 0r rburning urination Systemic Manifestation: fever, chills body malaise 3. Cystitis Special variants a. Interstitial Cystitis (Chronic pelvic pain syndrome) Persistent, painful chronic cystitis associated with inflammation and fibrosis of all layers of the bladder wall Fissures and punctuate haemorrhages (cystoscopy) Most frequent among women Intermittent, severe suprapubic pain, urinary frequency, urgency, hematuria, dysuria
c. Polypoid Cystitis
undego transformation of central epithelial cells Central epithelial cells become Cystitis glanduralis cuboidal or columnar
If untreated, 50% - 70% invade the underlying muscle b. Invasive Urothelial Cancer Extent of invasion is of prognostic significance
Cystitis cystica cystic spaces lined by urothelium 2. Squamous Metaplasia As a response to injury, the urothelium converts to a squamous epithelium which is a more durable lining. 3. Nephrogenic Adenoma Shed renal tubular cells implant at sites of injured urothelium Resembles renal tubules histologically Overlying urothelium may become cuboidal and papillary Tubular proliferation in the lamina propria
c.
Papilloma (1% or fewer) Small; superficially attached to the mucosa (exophythic papilloma) Lining is similar to normal urothelium Inverted papilloma extends into the lamina propria
d. Papillary Urothelial Neoplasm of Low Malignant Potential (PUNLMP) Histologically similar to papilloma but with thicker urothelium OR with diffuse nuclear enlargement Larger than papillomas; may grossly look like the low-grade & high-grade lesions
A. Urothelial (transitional Cell) Tumors 90% of bladder tumors Benign to malignant Precursor lesions of invasive urothelial carcinoma a. Non-invasive papillary tumors most common precursor which originates from papillary urothelial hyperplasia b. Carcinoma-in-situ Flat non-invasive urothelial carcinoma
Morphologi c patterns: Papilloma Invcasive papillary carcinoma Flat non-invasive carcinoma Flat invasive carcinoma Classificati on Carcinoma-in-situ
e.
Low-Grade Papillary Urothelial Carcinoma Cells are orderly and cohesive Mild nuclear atypia Infrequent mitosis High-Grade Papillary Urothelial Carcinoma Dyscohesive cells with large, hyperchromatic nuclei Loss of polarity (disorganized architecture) Frequent mitotic figures 80% are invasive
f.
B. Other Epethelial Tumors 1. Squamous Cell Carcinoma (3% - 7%) Pure or Mixed (Urothelial + squamous cell) Usually invasive and fungating or ulcerative Usually seen in cases of schistosoma haematobium infection
2. Adenocarcinoma Rare
Identical to adenocarcinomas seen in GIT Some arise from urachal remnants or in association with extensive intestinal metaplasia 3. Small-cell carcinoma
Indstinguihshable fom lung small cell carcinoma Arise in the bladder Associated with urothelial, squamous, or adenocarcinoma
Prostatic enlargement (men) Cystocele of the bladder (women) Urethral narrowing or stricture Inflammatory fibrosis and contractions in the bladder after cystitis Bladder tumors Calculi or other foreign bodies Neurogenic bladder
URETHRA
I. Urethritis
Gonococcal or Non-gonococcal
TIS carcinoma-in-situ T1 lamina propria invasion T2 muscularis propria invasion T3a microscopic extravesicle invasion T3b grossly apparent extravesicle invasion T4 invasion of adjacent structures
Embryonal rhabdomyosarcoma n ~ most common sarcoma in the bladder in infants and children ~ Manifest asa sarcoma botyroides (polypoid grapelike mass) Leiomyosarcoma most common sarcoma in the bladder adults
3. Peyronie disease
Fibrous bands involving corpus cavenosum of the penis
4. Urethral carccinoma
primary urethral carcinoma is uncommon Proximal urothelial