Adrenal Gland Pathology (Handorf) Flashcards

1
Q

What are the layers of the adrenal gl and what do they male

A

z. glomerulosa = mineralcorticoids - SALT
z. fasciuculata = glucocorticoids - SUGAR
reticulariz = estrogens and androgens - SEX

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2
Q

What determines the shape of the adrenals

A

configuration od surrounding organs

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3
Q

What shape would the adrenals be if a kidney was congenitally absent?

A

spherical

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4
Q

pituitary adenoma induced hypercorticalism

A

cushing’s disease

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5
Q

Distinguish cushing’s dz from cushing’s syndrome

A

syndrome is a state of ↑cortisol due to any cause

diseases is due to a pituitary adenoma that secretes ACTH

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6
Q

hypertension + hypokalemia

A

conn syndrome = excess aldosterone

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7
Q

conn syndrome can be caused by a aldosterone secreting…

A

cortical adrenal adenoma

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8
Q

precocious puberty in males

A

adrenogenital syndrome

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9
Q

pathophys of adrenogenital syndrome

A

21-hydroxylase or 11-beta-hydroxylase deficiency impairs the synthesis of cortisol and aldosterone, shunting precursors into androgen synthesis (no cortisol = no feedback inhibition to turn off pathway) → adrenal hyperplasia and increased testosterone

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10
Q

septic shock + DIC + adrenal hemorrhage =

A

Waterhouse-Friederichsen Syndrome

= acute adrenal insufficiency

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11
Q

what bug is most assc with Waterhouse-Friederichsen Syndrome

A

N. meningitis

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12
Q

etiologies of acute adrenal insufficiency

A
  1. Waterhouse-Friederichsen Syndrome
  2. sudden withdrawal of exogenous corticosteroids
  3. sudden stress + underlying chronic renal insufficiency
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13
Q

What is notable of H &E in a pt that suffered from Waterhouse-Friederichsen Syndrome

A

hemorrhages!! red everywhere!

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14
Q

widespread ecchymosis

A

DIC

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15
Q

Treatment for Waterhouse-Friederichsen Syndrome

A

abx and replacement of the hormones lost when the adrenals were wiped out—vasopressors

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16
Q
hyper-pigmentation 
hypotension (<110/70)
nausea
weight loss
appear emotional
A

chronic adrenal insufficiency disease… aka addisons

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17
Q

chronic adrenal insufficiency disease…

A

addisons

**primary or secondary

18
Q

notale electrolytes in acute adrenal insufficiency

A

hyperkalemia and hyponatremia

19
Q

why do pts with addison’s have hyperpigmentation?

A

↑ATCH = ↑MSH (melanocyte stimulating hormone)

20
Q

most common etiology of chronic adrenal insufficiency disease

A
US = autoimmune and hemachromatosis 
under-developed = TB
21
Q

notable labs in addisons

A

hyperkalemia, hyponatremia, metabolic acidosis, hypoglycemia

22
Q

treatment for addisons

A

hormone replacement therapy (catecholamines)

23
Q

causes of secondary chronic adrenal insufficiency disease

A
  • hypothalamic pituitary disease
  • neoplasm
  • infection
  • hypothalamic-pituitary suppression (long term steroid use, steroid producing neoplasms)
24
Q

What are the primary adrenal neoplasms of the cortex?

medulla?

A

cortex:

  • adrenal cortical ademoma
  • adrenal cortical carcinoma

medulla:

  • neuoblastoma
  • pheochromocytoma
25
Q

color or cortical neoplasms

A

yellow

26
Q

gross appearence of medullary neoplasms

A

redish with YELLOW RING

27
Q

grossly how can you tell if an adrenal cortical adenoma is functional? non-functional?

A

functional = the adjacent/oppostie gland is atrophic

non-functional = the adjacent/oppostie gland is hyperplastic

28
Q

most adrenal cortical carcinomas are (functional or non-functional)

A

functional… >90%

29
Q

what are clues to tell you that an adrenal cortical carcinoma is malignant?

A

> 5 cm in diameter
if there are mets…
they don’t really invade so thats not helpful

30
Q

characteristic histo of adrenal cortical carcinomas

A

bland, anaplastic, no mitoses

31
Q

most common extracranial solid tumor of childhood

A

neuroblastoma

32
Q

Where can neuoblastomas arise? What are the most common sites?

A

anywhere in the sympathetic nercous system or the brian

adrenals (medullary) and paraaotric ganglia

33
Q

neuroblastomas are (indolent, aggressive)

A

aggressive, they are rapidly dividing

34
Q

treatment for neurobalstoma

A

surger + chemo

35
Q

episodic HTN, palpitations

A

pheochromocytoma

36
Q

Where can pheochromocytomas arise?

A

paraganglionic system

37
Q

3 families of paraganglionic system (outside of the adrenals)

A

branchiometric, intravagal, aorticosympathetic

38
Q

adrenals are common sites of metastasis from

A

lung and breast

39
Q

___ and/or ___ tumors are almost certainly metastatic

A

multifocal and/or bilateral

40
Q

T or F: mets are the commonest malignant neoplasm in adrenals

A

true