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12 Cards in this Set

  • Front
  • Back
Gene locus associated with congenital adrenal hypoplasia:

Addison's starts to occur when how much of the gland is gone?

Most of Dr. Addison's patients had what infection?

Fungal infections that can cause Addisons:
DAX1/NROB1

80%

bovine TB of the adrenals

histoplasmosis, coccidioidomycosis, blasto
Addisons patients usually have Ab's against what?

Schmidt's (autoimmune polyglandular) I:

Locus for Schmidts:

Addisons + autoimmune diabetes or thyroid:
21-hydroxylase

hypo-PTH, Addison's, mucosal candidiasis

AIRE

Schmidt's II
Causes of iatrogenic Addison's:

Clinical signs for Addison's:

Lyte changes in Addison's:
too-rapid withdrawal of steroids, post-adrenectomy, ketoconazole/fluconazole therapy

weakness, N/V, fatigue, hyperpigmentation

low Na+, high K+, metabolic acidosis, low BS, cortisol
What is the usual problem in selective hypoaldosteronism?

pathology of Addison's crisis:

hermorrhage, fibrin thrombi, necrosis of the adrenals usually due to sepsis:

Usualy bacterial causes?
JGA in kidney not producing enough renin

sudden collapse and shock with peripheral vasodilation, high CO

Waterhouse-Freidrichsen syndrome

Meningicoccus, staph, S pneumo, H flu
basophilic microadenoma in pituitary:

rapid enlargement of a pituitary adenoma leading to hyperpigmentation, blindness, death:

Other malignancies that classically can produce ectopic ACTH:
ACTh producing tumor (Cushing's)

Nelson's syndrome

oat-cell of lung, bronchial/thymic carcinoids, medullary thyroid carcinoma
Heavy negative feedback on pituitary basophilic ACTH cells produces what?

Why do patients with hyperaldosteronism usually not have edema?

These patients can die from use of what diuretic?
Crooke's hyaline change

aldosterone's effect overridden by ANP

Thiazides
What is the deficiency in apparent mineralocorticoid excess syndrome?

Secondary hyperaldosteronism is due to what?
11-B-hydroxylase dehydrogenase type 2 deficiency

CHF, cirrhosis, nephrotic syndrome, Goldblatt's HTN
CAH with no cortisol, aldosterone, or DOC - salt wasting:

CAH with high DOC, causing salt retention, HTN:

Classic mainstay of therapy for adrenal cortical carcinomas:

Two major tumors of the adrenal medulla:
21-hydroxylase deficiency

11-B-hydroxylase deficiency

mitotane - DDT analog

pheo, neuroblastoma
How did pheochromocytoma get its name?

Stain for pheo?

Classic screen for pheo?

Most sensitive?
colorful rxn in chromium salts

chromogranin, synaptophysin

24 hr urine VMA

plasma free metanephrine
Parathyroid, Pituitary, Pancreas:

Parathyroid, adrenal medullary tumor, thyroid carcinoma producing calcitonin:

Marfanoid body type, mucosal neuromas:
MEN I

MEN IIa

MEN IIb(III)
Unique facts about pheo/neuroblastoma frozen section:

reaction with formalin?
acid fast, autofluorescent

fluoresces yellow-green from catecholamines getting altered
"Blueberry muffin baby":

better-differentiated neuroblastomas stain for what?

classic test for neuroblastoma?
neuroblastoma patient with multiple skin mets

enolase, S-100, synaptophysin

urine HVA, VMA