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Integrated Endocrine Pathology — Endocrine
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Integrated Endocrine Pathology
Endocrine · Integrated Endocrine Pathology · medium
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Integrated Endocrine Pathology MCQs: practice questions
Sample Integrated Endocrine Pathology multiple-choice questions from Endocrine.
A renal-adrenal mass in a patient with VHL syndrome is accompanied by a catecholamine-producing tumor. The adrenal tumor is:
- A. Pheochromocytoma
- B. Adrenal cortical carcinoma
- C. Ganglioneuroma
- D. Neuroblastoma
- E. Adrenal cortical adenoma
A patient with autoimmune adrenalitis has hyperpigmentation and hypotension. The diagnosis is:
- A. Pheochromocytoma
- B. Primary hyperaldosteronism
- C. Secondary adrenal insufficiency
- D. Cushing disease
- E. Primary adrenal insufficiency
A patient with severe hypothyroidism develops non-pitting edema. The diagnosis is:
- A. Thyroid storm
- B. Cushing syndrome
- C. Myxedema
- D. Acromegaly
- E. Addison disease
A patient develops acute adrenal insufficiency after bilateral adrenal hemorrhage. Which electrolyte pattern is expected?
- A. Normal electrolytes in every case
- B. Hypernatremia and hyperkalemia
- C. Hypercalcemia and hypokalemia
- D. Hyponatremia and hyperkalemia
- E. Hypernatremia and hypokalemia
An endocrine tumor syndrome featuring parathyroid, pituitary, and pancreatic neuroendocrine tumors is:
- A. MEN 2A
- B. MEN 2B
- C. VHL syndrome
- D. MEN 1
- E. Li-Fraumeni syndrome
An elderly patient has a rapidly enlarging thyroid mass causing dysphagia and airway compression. The most likely diagnosis is:
A patient with medullary thyroid carcinoma should be evaluated for a mutation in:
A patient has enlarged hands, coarse facial features, and increased IGF-1. The underlying pituitary lesion is most likely:
A patient has hyperthyroidism, diffuse thyroid enlargement, and exophthalmos. The diagnosis is:
A patient has hypertension, hypokalemia, and suppressed renin. Which adrenal disorder is most likely?
A patient with pancreatic neuroendocrine tumor develops diabetes and gallstones. The tumor is:
A patient with pancreatic neuroendocrine tumor develops watery diarrhea and hypokalemia. The tumor is:
A patient with polyuria has low ADH due to posterior pituitary dysfunction. The diagnosis is:
A large pituitary mass causes bitemporal hemianopia. The structure compressed is the:
Postpartum hemorrhage is followed by failure to lactate and amenorrhea. The likely diagnosis is:
A patient with a thyroid nodule has nuclear grooves and psammoma bodies. The diagnosis is:
A child with adrenal hyperplasia has virilization and elevated 17-hydroxyprogesterone. The defect is most likely:
A thyroid tumor invades its capsule and blood vessels. The most likely diagnosis is:
MEN 2B is distinguished from MEN 2A by the presence of:
A patient with autoimmune thyroiditis develops a thyroid mass. Which malignancy is particularly associated?
A patient with MEN 2A is most likely to have medullary thyroid carcinoma, pheochromocytoma, and:
A patient with a pituitary adenoma has markedly elevated prolactin and galactorrhea. The tumor is:
A patient has weight gain, proximal muscle weakness, hypertension, and hyperglycemia due to a pituitary ACTH adenoma. The diagnosis is:
A thyroid tumor contains calcitonin-producing cells and amyloid stroma. The diagnosis is:
A patient with pancreatic neuroendocrine tumor develops necrolytic migratory erythema. The tumor is:
A patient has episodic headache, sweating, palpitations, and severe hypertension. The most likely tumor is:
A patient with acromegaly has elevated GH and IGF-1. Which finding is expected pathologically?
A patient with fasting hypoglycemia has inappropriately elevated insulin and C-peptide. The likely tumor is:
A patient with recurrent peptic ulcers and markedly elevated gastrin has a pancreatic neuroendocrine tumor. The diagnosis is:
A patient with MEN 1 has hypercalcemia, a pituitary adenoma, and recurrent peptic ulcers. The pancreatic tumor is most likely: