Endocrine syndromes and diseases Flashcards

1
Q

glucocorticoids in cushing’s disease and cushing’s syndrome come from where

A

zona fasiculata

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2
Q

hypercortisolism occurs as result of hypersecretion of ACTH from pituitary adenoma

A

cushing’s disease

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3
Q

MC cause of cushing’s syndrome is what

A

administration of exogenous steroid hormones

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4
Q

70% of cushing’s syndrome caused by what

A

cushing’s disease

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5
Q

excess glucocorticoids for reason other than pituitary

A

cushing’s syndrome

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6
Q

MC source of ectopically secreted ACTH

A

extrapituitary tumors like SCLC

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7
Q

S&S of cushing’s

A
moon face
buffalo hump
red face
HTN
thin skin (abdominal striae)
glucose intolerance
DM
mentally unstable
fatigue/weakness
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8
Q

S&S of conn’s syndrome

A

retention of sodium
loss of potassium
retention fo water
hypernatremic hypokalemic HTN

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9
Q

adenoma of zona glomerulosa

A

primary hyperaldosteronism

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10
Q

what stimulates secretion of aldosterone

A

angiotensin

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11
Q

associated with hyperreninemia

A

secondary hyperaldosteronism

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12
Q

21-hydroxylase deficiency in neonates

A

adrenogenital syndrome

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13
Q

adrenogenital syndrome in females experience what

A

virilization due to excess adrenogenic hormones

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14
Q

what are the S&S of adrenogenital syndrome in adults females

A

hirsutism, deepening of the voice, loss of menstruation

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15
Q

adrenocortical hypofunction is a consequence of what

A

adrenal destruction

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16
Q

what infections and malignancies cause adrenal insufficiency

A

TB
histoplasmosis
lung or breast cancer

17
Q

bilateral adrenal rupture

A

waterhouse friedrichsen syndrome

18
Q

what causes waterhouse friedrichsen syndrome

A

neisseria meningitides

19
Q

what is the MC disease of adrenal insufficiency

A

addison’s disease

20
Q

infiltration of lymphocytes and plasma cells in the cortex

A

addison’s disease

21
Q

what S&S do addison’s disease pts have

A

fatigue
weight loss
nausea
hypotension

22
Q

neoplasms of the adrenal medulla that synthesize and release catecholamines (Epi and NE)

A

pheochromocytoma

23
Q

pheochromocytomas that arise from other sites are called what

A

paragnagliomas

24
Q

dominant clinical manifestation of pheochromocytomas

A

HTN abrupt with tachycardia, palpitations, H/A, sweating, and tremor

25
Q

2/3 of pheochromocytoma pts have what

A

chronic, sustained elevations in BP

26
Q

in another 1/3 of pheochromocytoma pts, paroxysms may be precipitated by what

A

stress, exercise, and change in posture

27
Q

elevations in BP induced by sudden release of what

A

catecholamines

28
Q

pheochromocytomas may secrete what other hormones

A

ACTH and somatostatin

29
Q

lab dx of pheochromocytomas is based on increased urinary excretion of what

A

VMAs and metanephrines