2 - Anterior Pituitary 1 Flashcards

1
Q

which pituitary hormones are grouped together by differentiation pathways?

A

GH and prolactin
TSH and LH/FSH
ACTH and melanotropes

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2
Q

common alpha subunit is shared by what hormones?

A

TSH, LH, FSH, beta-HCG

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3
Q

size cutoff btwn micro and macroadenoma in pituitary

A

1 cm

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4
Q

4 MC pituitary adenoma cell types / secretion types

A

35% prolactin
28% “non functioning” (alpha subunit)
17% GH
9% ACTH

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5
Q

visual field defect assoc w/ pituitary tumor

A

superior temporal quadrantanopsia or temporal hemianopsia

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6
Q

sx of hyperprolactinemia

A

women: galactorrhea, amenorrhea
men: dec libido, impotence, rarely have galactorrhea

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7
Q

causes of hyperprolactinemia (fairly general)

A

PREGNANCY (must r/o before working up for prolactinoma)
hypothyroidism (TRH stimulates prolactin release)
prolactinoma
other pituitary masses interfering w/ DA inhibition
cosecretion w/ GH (ex in acromegaly)
anti dopaminergic drugs
chronic renal failure

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8
Q

Hook effect

A

immunoassays can give false negs if levels of target are too high - abs get covered by so much antigen that nothing can agglutinate

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9
Q

only pituitary adenoma where surg is not considered first line tx

A

prolactinoma

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10
Q

tx of prolactinoma

A

dopamine agonists - bromocriptine (used in pregnancy but causes nausea and orthostasis), cabergoline (better tolerated)

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11
Q

cabergoline

A

DA agonist used for hyperprolactinemia

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12
Q

normal stimuli for GH secretion

A

diurnal - inc during sleep

physical activity and emotional stress stimulate it

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13
Q

what molecule mediates most growth effects of GH?

A

insulin like growth factor 1 (IGF-1)

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14
Q

GH effects independent of IGF1

A

glucose homeostasis (insulin resistance), Ca metab (inc bone density), lipolysis

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15
Q

cause of GH excess

A

mostly sporatic adenomas

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16
Q

causes of sx in GH excess

A

neuropathy
enlarged visceral organs (heart important here)
glucose intolerance

17
Q

how to dx acromegaly

A

single serum GH > 100 ng/ml (rarely done b/c often dont catch it)
elevated IGF-1 (longer half life so more sensitive)

18
Q

medical therapy for acromegaly

A

somatostatin analogues - octreotide, etc
pegvisomant (GH-R antagonist)
dopamine agonist (bromocriptine, cabergoline)

19
Q

complications of acromegaly

A

inc mortality rate (2-3x)
often CV problems, respiratory, inc risk of malignancy
can develop overt DM

20
Q

McCune Albright

A

inherited cause of GH pituitary adenoma
G protein subunit mutation
cafe au lait spots, precocious puberty, acromegaly/gigantism, thyrotoxicosis

21
Q

Carney Complex

A

inherited cause of GH pituitary adenoma
PKA type 1 regulatory subunit problem
spotty skin pigmentation and blue nevi, cardiac myxomas, schwannomas, testicular/ovarian tumors

22
Q

Multiple endocrine neoplasia (MEN 1)

A

AD inheritance
menin gene mutation (tumor suppressor)
3 Ps - pituitary adenoma (mostly prolactin, next MC is GH), parathyroid hyperplasia, pancreatic neuroendocrine tumors (mostly gastrinoma, maybe insulinoma)