Adrenal Case Review Flashcards
Hypercortisolic patient, why do they have hypoK and HTN
why do they have polyuria/polydipsia
Cortisol has MC activity
seconday coms of diabetes/hyperGly
Etiologies of hypercortisol
Exogenous GC
Pituitary hypersecretion of ACTH
Ectopic ACTH from neoplasm
Hypersecretion of cortsiol by adrenal adenoma/carcinoma
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
Adrenal problem
ACTH secreting tumor
ACTH dependent cortisol excess
undetectable
Comps of Cushing’s syndrome
M I O D I
metabolic syndrome Inc CV risk Osteoporosis Depression Impaired gonad fxn
Suspected hypercortisol
1st step
2nd step
ACTH low means, next step
ACTH high/normal indivates
next step
confirm cortisol excess
Check ACTH
adrenal cause, imaging
pituitary/ectopic
HD DM suppression
suppressed- image pituitary
not- look for ca
Possible metabolic causes of Addisons dz
lab studies for Addisons
GC insufficiency
MC insufficiency
ACTH stim test w
CAH, enzyme inhibitors (metyrapone, keto, aminoglutethimide)
low AM cortisol, failed ACTH stim test, high ACTH (primary dz)
low Na, high K
cosyntropin
Addisons z
Pt w secondary/tertiary insufficiency are not
have near normal synth of ____, not markedly
hyperpigmented (low ACTH)
aldo, hypoNa/hyperK
Addison’s Crisis presentation
precipitated by
Tx w
Loss of adrenal fxn, N/V/ab pain, hypoTN, hypovolemic shock/death
sepsis, surgical stress
MC/GC replacement
Pt with suspected pheo, hyperCa can indicate
MEN 2A