Professional Documents
Culture Documents
Endocrine
Questions
EMBRYOLOGY
1. Which structure connects the thyroid gland with the tongue in early embryos? (p 320) __________
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2. How can you differentiate a thyroglossal duct cyst from a branchial cleft cyst? (p 320) __________
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ANATOMY
3. What are the three major zones of the adrenal cortex? Name the hormone secreted by each zone.
(p 320) ________________________________________________________________________
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4. What are the two divisions of the pituitary gland? List the hormones secreted by each division?
(p 321) ________________________________________________________________________
5. Where are the cell bodies that produce the hormones released by the posterior pituitary gland?
(p 321) _______________________________________________________________________
6. What are the three major cell types in the Islets of Langerhans? Name the hormone secreted by
______________________________________________________________________________
PHYSIOLOGY
7. Which two cell types have their glucose transport primarily controlled by insulin? By which specific
8. What test will allow you to distinguish between high endogenous and high exogenous insulin?
(p 322) ________________________________________________________________________
9. Fill in the blanks and choose the correct answers to complete the mechanism by which β cells secrete
insulin. (p 322)
10. Which two molecules control the secretion of prolactin? Which hormone does prolactin control the
secretion of? (p 323) _____________________________________________________________
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11. What are the effects of antidiuretic hormone (vasopressin) on fluid volume and serum sodium con-
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12. For each of the congenital bilateral adrenal hyperplasias in the chart, indicate whether blood
pressure and sex hormone levels are increased or decreased. (p 326)
13. What enzyme catalyzes the conversion of testosterone to estradiol? What enzyme catalyzes the
14. Describe the regulation of cortisol secretion, including the relevant anatomic locations, cell types,
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15. Where does the inactive form of vitamin D come from? Where do the two hydroxylation steps
serum calcium level and _______________ (increases/decreases) serum phosphate levels. (p 328)
17. How do T3 and T4 control the body’s metabolic rate? (p 329) ______________________________
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18. What is the difference between thyroid-binding globulin and thyroglobulin? (p 329) _____________
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PATHOLOGY
20. What is the most common cause of Cushing syndrome? (p 331) __________________________
21. For a patient who is not taking steroids, what are other potential causes of Cushing syndrome?
(p 331) ________________________________________________________________________
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22. What are the common clinical manifestations of Cushing syndrome? (p 331) _________________
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25. What are the three common causes of Waterhouse-Friderichsen syndrome? (p 332) ___________
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26. What is the “rule of 10’s” for pheochromocytoma? What is the cell of origin for this tumor? (p 334)
______________________________________________________________________________
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27. What are the signs and symptoms of pheochromocytoma? (p 334) _________________________
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28. What is the primary symptom of the VIPoma neuroendocrine tumor, which secretes vasoactive
29. Compare and contrast the characteristics of hypothyroidism vs hyperthyroidism, using the chart.
(p 335)
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31. What is the difference between de Quervain thyroiditis and Riedel thyroiditis? (p 336) __________
______________________________________________________________________________
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33. Name four types of thyroid cancer. Which is most common? (p 338) ________________________
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36. What does the mnemonic “stones, thrones, bones, groans, and psychiatric overtones” stand for?
(p 340) ________________________________________________________________________
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39. What are the differences between DI and SIADH? (p 342) ________________________________
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40. What are the acute manifestations of diabetes mellitus type 1? (p 344) ______________________
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41. What are the chronic manifestations of poorly controlled diabetes? (p 344) ___________________
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42. Compare and contrast the characteristics of type 1 vs type 2 diabetes, using the chart. (p 345)
Type 1 Type 2
Associated with obesity
Genetic predisposition
Glucose intolerance
Ketoacidosis
Need for insulin
Primary defect
Sensitivity to insulin
Typical age of onset
43. How can patients with diabetic ketoacidosis be recognized by their breath? (p 345) ____________
______________________________________________________________________________
44. What are the signs and symptoms of carcinoid syndrome? (p 346) _________________________
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45. In the chart, check which components are involved in the multiple endocrine neoplasias. (p 347)
PHARMACOLOGY
46. Name the three varieties of fast-acting insulin. What is the main use of fast-acting insulin compared
to long-acting insulin? (p 348) ______________________________________________________
______________________________________________________________________________
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47. What is the most feared complication of metformin? Which patients have the highest risk? (p 348)
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48. Among insulin, metformin, sulfonylureas, and glitazones/thiazolidinediones, which can cause
Answers
EMBRYOLOGY
1. Thyroglossal duct (a common site of ectopic thyroid tissue).
2. A thyroglossal duct cyst will move with swallowing whereas a branchial cleft cyst will not.
ANATOMY
3. Zona glomerulosa produces aldosterone, zona fasciculata produces cortisol, and zona reticularis
produces sex hormones.
4. Posterior pituitary: ADH (vasopressin), oxytocin. Anterior pituitary: FSH, LH, ACTH, TSH, prolactin,
GH, and β-endorphin. MSH is secreted from intermediate lobe of pituitary.
5. The hypothalamus.
6. β cells produce insulin. α cells produce glucagon, and δ cells produce somatostatin.
PHYSIOLOGY
7. Skeletal myocytes and adipocytes; by the GLUT4 transporter.
8. C-peptide is absent if the source of insulin is exogenous and present in high levels if the patient has
an insulinoma.
9.
III. ATP dependent potassium channels close, causing depolarization of the cell membrane.
V. Calcium enters the cell, disinhibiting the release of insulin-containing vesicles docked at
the cell membrane.
10. Dopamine inhibits prolactin release; TRH stimulates. Prolactin inhibits GnRH, thus inhibiting the
hypothalamic-pituitary-gonadal axis.
11. ADH leads to increased fluid volume and decreased serum sodium concentration. Of the two,
decreased serum sodium concentration and osmolality is more unique to ADH (aldosterone also
increases fluid volume).
12.
14. CRH stimulates release of ACTH in anterior pituitary, which prompts cortisol production in the zona
fasciculata of the adrenal cortex.
15. Inactive Vitamin D is absorbed from the diet or is synthesized in the skin when exposed to sunlight.
Activation of Vitamin D requires hydroxylation in the liver, then the kidney.
17. By increasing Na+/K+-ATPase activity, which increases oxygen consumption, respiratory rate, and
body temperature.
18. Thyroid-binding globulin is a transport protein that carries T4 and T3 through the bloodstream
(because they’re lipophilic). Thyroglobulin is a large precursor molecule synthesized by thyroid
follicles that is used to generate multiple T4 and T3 molecules.
PATHOLOGY
20. Exogenous corticosteroids.
21. Cushing disease (pituitary adenoma): 70%; ectopic ACTH (eg, small cell lung cancer): 15%;
adrenal tumor: 15%.
22. Weight gain (truncal obesity), moon facies, buffalo hump, skin thinning, striae, hypertension,
hyperglycemia, osteoporosis, amenorrhea, and immunosuppression.
26. 10% are malignant, 10% are bilateral, 10% are extra-adrenal, 10% calcify, and 10% occur in kids.
Chromaffin cells are the cells of origin for pheochromocytoma.
27. Elevated blood Pressure, Pain (headache), Perspiration, Palpitations (tachycardia), and Pallor.
These “5 P’s” are episodic.
29.
Chest pain,
Bradycardia; dyspnea
Cardiovascular changes palpitations,
on exertion
arrhythmias
T3 uptake ↓ ↑
30. Hashimoto thyroiditis, postpartum thyroiditis, cretinism, de Quervain thyroiditis, and Riedel
thyroiditis.
31. de Quervain (subacute) thyroiditis is a self-limited type of hypothyroidism that follows a flu-like
illness. Riedel thyroiditis involves fibrous replacement of the thyroid.
33. Papillary thyroid carcinoma (most common), follicular, medullary, and anaplastic.
34. In hypoparathyroid patients, tapping of the facial nerve causes the facial muscles to contract.
36. Renal calcium stones, polyuria (thrones), osteitis fibrosa cystica of bones, neuropsychiatric
disturbances (“psychiatric overtones”), and abdominal complaints (groans due to constipation).
37. Water deprivation test: urine osmolality doesn’t increase in response to water deprivation.
Response to desmopressin can distinguish between central and nephrogenic DI.
38. Ectopic ADH (eg, small cell lung cancer), CNS disorder/head trauma, pulmonary disease, and
drugs such as cyclophosphamide.
39. DI denotes lack of ADH; SIADH denotes too much ADH. DI is characterized by intense thirst and
polyuria, with high serum osmolarity and low urine concentration. SIADH is characterized by
excessive water retention, with high urine osmolarity and low serum osmolarity.
40. Polydipsia, polyuria, polyphagia, weight loss, DKA (type 1), and hyperosmolar hyperglycemic state
(type 2).
42.
Type 1 Type 2
Associated with obesity No Yes
Genetic predisposition Weak Strong
Glucose intolerance Severe Mild to moderate
Ketoacidosis Common Uncommon
Need for insulin Always Sometimes
Primary defect Destruction of β cells Increased resistance to insulin
Sensitivity to insulin High Low
Typical age of onset <30 years >40 years
43. Increased ketogenesis results in accumulation of acetone and other ketones; when exhaled,
acetone gives breath a fruity odor.
44. Diarrhea, cutaneous flushing, asthmatic wheezing, and right-sided valvular disease.
45.
PHARMACOLOGY
46. Insulin aspart, lispro, and glulisine. Unlike long-acting insulin, which is used to maintain a normal
basal insulin level, fast-acting insulin is taken with meals to address abnormally elevated
postprandial glucose.
47. Lactic acidosis, especially in patients with renal insufficiency) or B12 deficiency.
51. Sevelamer.