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
color or cortical neoplasms
yellow
26
gross appearence of medullary neoplasms
redish with YELLOW RING
27
grossly how can you tell if an adrenal cortical adenoma is functional? non-functional?
functional = the adjacent/oppostie gland is atrophic non-functional = the adjacent/oppostie gland is hyperplastic
28
most adrenal cortical carcinomas are (functional or non-functional)
functional... >90%
29
what are clues to tell you that an adrenal cortical carcinoma is malignant?
> 5 cm in diameter if there are mets... they don't really invade so thats not helpful
30
characteristic histo of adrenal cortical carcinomas
bland, anaplastic, no mitoses
31
most common extracranial solid tumor of childhood
neuroblastoma
32
Where can neuoblastomas arise? What are the most common sites?
anywhere in the sympathetic nercous system or the brian adrenals (medullary) and paraaotric ganglia
33
neuroblastomas are (indolent, aggressive)
aggressive, they are rapidly dividing
34
treatment for neurobalstoma
surger + chemo
35
episodic HTN, palpitations
pheochromocytoma
36
Where can pheochromocytomas arise?
paraganglionic system
37
3 families of paraganglionic system (outside of the adrenals)
branchiometric, intravagal, aorticosympathetic
38
adrenals are common sites of metastasis from
lung and breast
39
___ and/or ___ tumors are almost certainly metastatic
multifocal and/or bilateral
40
T or F: mets are the commonest malignant neoplasm in adrenals
true