Adrenal Case Review Flashcards

1
Q

Hypercortisolic patient, why do they have hypoK and HTN

why do they have polyuria/polydipsia

A

Cortisol has MC activity

seconday coms of diabetes/hyperGly

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2
Q

Etiologies of hypercortisol

A

Exogenous GC
Pituitary hypersecretion of ACTH
Ectopic ACTH from neoplasm
Hypersecretion of cortsiol by adrenal adenoma/carcinoma

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3
Q

Hypercortisolemia pt, ACTH levels <5 indicate

> 20 indicate

ACTH level that is normal o high can indivate

in the presence of high cortisol, normal indiv ACTH levels should be

A

Adrenal problem

ACTH secreting tumor

ACTH dependent cortisol excess

undetectable

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4
Q

Comps of Cushing’s syndrome

M
I
O
D
I
A
metabolic syndrome
Inc CV risk
Osteoporosis
Depression
Impaired gonad fxn
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5
Q

Suspected hypercortisol

1st step
2nd step

ACTH low means, next step
ACTH high/normal indivates

next step

A

confirm cortisol excess
Check ACTH

adrenal cause, imaging
pituitary/ectopic

HD DM suppression
suppressed- image pituitary
not- look for ca

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6
Q

Possible metabolic causes of Addisons dz

lab studies for Addisons

GC insufficiency

MC insufficiency

ACTH stim test w

A

CAH, enzyme inhibitors (metyrapone, keto, aminoglutethimide)

low AM cortisol, failed ACTH stim test, high ACTH (primary dz)

low Na, high K

cosyntropin

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7
Q

Addisons z

Pt w secondary/tertiary insufficiency are not

have near normal synth of ____, not markedly

A

hyperpigmented (low ACTH)

aldo, hypoNa/hyperK

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8
Q

Addison’s Crisis presentation

precipitated by

Tx w

A

Loss of adrenal fxn, N/V/ab pain, hypoTN, hypovolemic shock/death

sepsis, surgical stress

MC/GC replacement

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9
Q

Pt with suspected pheo, hyperCa can indicate

A

MEN 2A

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