adrenal pathology Flashcards

1
Q

solitary, well-circumscribed, yellow-orange lesions within adrenal cortex or protrude into medulla

A

adrenal cortical adenoma

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2
Q

functional adenomas are____

A

atrophied

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3
Q

non-functional adenoma are____

A

normal thickness

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4
Q

vacuolated, lipid rich tumor cella, mild pleomorphism

A

adrenal cortical adenoma

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5
Q

lesions that are yellow on cut surface, but usu contain areas of hemorrhage, cystic change, and necrosis

A

adrenal cortical carcinomas

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6
Q

carcinoma or adenoma: invade vascular channel, with metastases

A

carcinoma

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7
Q

where do adrenal cortical carcinomas like to metastasize to?

A

lungs

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8
Q

if you see anaplasia on histo of adrenal cortex, it is likely_____

A

carcinoma

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9
Q

define anaplasia

A

lack of differentiation

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10
Q

how to differentiate adrenal cortical carcinoma from adenoma? (5)

A
  1. metastases
  2. large size
  3. necrosis
  4. mitotic figures
  5. vascular invasion
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11
Q

adrenal cortex that is yellow, thickened and multinodular

A

adrenal cortical hyperplasia

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12
Q

caused by elevation in glucocorticoid/cortisol levels

A

cushings

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13
Q

a solitary, small, encapsulated aldosterone secreting adenoma

A

Conn syndrome

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14
Q

what accounts for 65% of primary hyperaldosteronism?

A

conn syndrome

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15
Q

clinical signs of hyperaldosteronism (4)

A
  1. HTN
  2. hypokalemia
  3. high aldosterone
  4. low blood renin
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16
Q

addison disease is primary acute OR chronic adrenocortical insufficiency

A

primary chronic adrenocortical insufficiency

17
Q

septicemic infxn caused by N. meningitidis infxn that results in massive adrenal hemorrhage in children

A

waterhouse-friderichsen syndrome

18
Q

waterhouse-friderichsen syndrome is more common in ____ vs addison disease which is more common in _____

A

children; adults

19
Q

causes of addisons (3)

A
  1. TB
  2. fungi
  3. metastatic neoplasms
20
Q

morphology with small glands, lipid depletion, lymphocytic infiltrate in cortex

A

addison disease

21
Q

presentation: fatigue, hyperpigmentation, N/V, hypotension, high potassium, low Na, elevated ACTH

A

addison disease

22
Q

morphologically, sedonary adrenocortical insufficiency spares the ____ and _____

A

zona glomerulosa and medulla

23
Q

uncommon neoplasms assc’d with incr catecholamine production and HTN

A

pheochromocytomas

24
Q

the cut surface is pale gray/brown, assc’d with hemorrhage, necrosis, cystic change, highly vascular tumors

A

pheochromocytoma

25
Q

neuroendocrine markers for pheochromocytoma (2)

A
  1. synaptophysin

2. chromogranin

26
Q

clinical presentation: abrupt HTN, sweating, tremor, HA, tachycardia, palpitations

A

pheochromocytoma

27
Q

dx of pheochromocytoma (2)

A
  1. urinary & serum catecholamines

2. MIBG scan

28
Q

amplification of N-Myc oncogene

A

neuroblastoma

29
Q

neuroblastoma is characerized by ___HTN, incr urine ____

A

diastolic; VMA/HNA

30
Q

homer-wrigth rosettes

A

neuroblastoma