Endocrine 2 practice Flashcards

(30 cards)

1
Q

What is the most common cause of hyperprolactinemia?
a) Prolactinoma
b) Hypothyroidism
c) Acromegaly
d) Renal failure
e) Pregnancy

A

a) Prolactinoma

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2
Q

What is the first line treatment for adenoma-induced hyperprolactinemia? Select two
a) Cabergoline
b) Metoclopramide
c) Bromocriptine
d) Promethazine
e) Prochlorperazine
f) Octreotide
g) Lanreotide
h) Phenoxybenzamine
i) Phentolamine

A

a) Cabergoline
c) Bromocriptine

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3
Q

What is NOT one of the three tests you do to diagnose a GH tumor?
a) Insulin-like growth factor test
b) Low-dose dexamethasone suppression test
c) Prolactin levels
d) Oral glucose suppression test

A

b) Low-dose dexamethasone suppression test

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4
Q

What is the first line Tx for GH tumors that cannot be resected? Select two
a) Cabergoline
b) Metoclopramide
c) Bromocriptine
d) Promethazine
e) Prochlorperazine
f) Octreotide
g) Lanreotide
h) Phenoxybenzamine
i) Phentolamine

A

f) Octreotide
g) Lanreotide

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5
Q

Those with post partum hemorrhage may experience what?
a) GH deficiency
b) Hyperprolactinemia
c) Hypopituitarism
d) Hypocortisolism
e) Hypercortisolism
f) SIADH
g) DI

A

c) Hypopituitarism

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6
Q

What is the correct order of the 4 tests for hypercortisolism?

A

1) Late night cortisol or 24-hour urine (most specific)
2) Low-dose dexamethasone suppression test
3) ACTH
4) High-dose dexamethasone suppression test

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7
Q

Define Addison’s disease (choose the best answer).
a) Primary adrenal insufficiency (low aldosterone and cortisol, high ACTH)
b) Secondary adrenal insufficiency (low cortisol, normal aldosterone and ACTH)

A

a) Primary adrenal insufficiency (low aldosterone and cortisol, high ACTH)

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8
Q

What two things should you use to Tx Addison’s disease?
a) Dexamethasone
b) Hydrocortisone
c) Prochlorperazine
d) Fludrocortisone
e) Lanreotide

A

b) Hydrocortisone
d) Fludrocortisone

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9
Q

You get a patient’s 8am renin and cortisol levels because you think they have Addison’s. Their renin is high. You then do a high-dose ACTH cosyntropin stim test and their cortisol does not rise.
What is the suspected diagnosis?
a) Addison’s
b) Secondary hypocortisolism

A

a) Addison’s

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10
Q

Which of the following is NOT a part of the triad of hyperaldosteronism?
a) Hypokalemia
b) Hypertension
c) Hypotension
d) Metabolic alkalosis

A

c) Hypotension

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11
Q

Renal hypoperfusion, like in CKD, may cause what?
a) Hypercortisolism
b) Hypocortisolism
c) Hyperaldosteronism
d) Hypoaldosteronism
e) SIADH

A

c) Hyperaldosteronism

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12
Q

How is hyperaldosteronism treated? (1st line and 2nd line Txs)

A

1st line = Spironolactone
2nd line = ACE inhibitors, CCBs

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13
Q

Subarachnoid hemorrhage and small cell lung cancer may cause what?
a) Hypercortisolism
b) Hypocortisolism
c) Hyperaldosteronism
d) Hypoaldosteronism
e) SIADH
f) DI

A

e) SIADH

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14
Q

A patient has euvolemic hypoosmolar hyponatremia. What condition should you suspect?
a) Hypercortisolism
b) Hypocortisolism
c) Hyperaldosteronism
d) Hypoaldosteronism
e) SIADH
f) DI
g) Pheochromocytoma

A

e) SIADH

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15
Q

Conivaptan and tolvaptan can correct moderate-severe what?
a) Hyponatremia
b) Hypernatremia
c) Hypovolemia
d) Hypervolemia

A

a) Hyponatremia

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16
Q

You give a patient you suspect has DI ADH. Their urine osmolality rises. What is the result of this test?
a) They have psychogenic polydipsia
b) They have DI

A

a) They have psychogenic polydipsia

17
Q

Which of the following is a catecholamine-secreting adrenal tumor of chromaffin cells?
a) Pituitary adenoma
b) Pheochromocytoma
c) Adrenocortical Carcinoma (ACC)
d) Paraganglioma

A

b) Pheochromocytoma

18
Q

Phenoxybenzamine and Phentolamine, then beta blockers/ CCBs, are the treatment for what?
a) Hypercortisolism
b) Hypocortisolism
c) Hyperaldosteronism
d) Hypoaldosteronism
e) SIADH
f) DI
g) Pheochromocytoma

A

g) Pheochromocytoma

19
Q

Which is matched appropriately?

1) MEN 1 = assoc with RET proto-oncogene .
-MEN 2 = aka Wermer’s syndrome, assoc with Menin gene defect.

2) MEN 1 = aka Wermer’s syndrome, assoc with Menin gene defect.
-MEN 2 = assoc. with RET proto-oncogene

A

2) MEN 1 = aka Wermer’s syndrome, assoc with Menin gene defect.
MEN 2 = assoc. with RET proto-oncogene

20
Q

T/F: With the oral glucose suppression test, growth hormone levels increase in acromegaly.

21
Q

T/F: Most pituitary tumors are posterior.

A

False (anterior)

22
Q

T/F: Cabergoline is successful for tumors that secrete prolactin and/or GH.

A

True (but surgery is first line Tx)

23
Q

T/F: Amenorrhea, infertility, vaginal dryness, galactorrhea, and hypogonadism are all Sx of hyperprolactinemia.

24
Q

T/F: Secondary hypercortisolism is an ACTH dependent illness.

25
T/F: Ketoconazole may cause hypercortisolism
False (may cause Addison’s)
26
T/F: Hyperkalemia may occur due to low cortisol
False (may be due to low aldosterone)
27
T/F: Normally, giving salt would decrease aldosterone
True
28
T/F: In SIADH, pts have concentrated blood, dilute urine, and high sodium
False (it’s the opposite)
29
T/F: For Central DI, desmopressin is first line Tx, and carbamazepine is second line
True
30
T/F: Parathyroid, pancreas, and pituitary can all be affected by MEN I
True