Endocrine Flashcards

1
Q

PDT for primary hyperaldosteronism

A

Etiology: Bilateral Adrenal Hyperplasia or unilateral adrenal adenoma
P:hypertension (tx resistant), hypokalemic alkalosis (reslting in muscle weakness + parasthesias)
Dx: Elevated plasma aldosterone, low plasma renin, aldosterone remains elevated following oral salinel load

Work up: CT to ID b/l adrenal hyperpalasia vs. adrenal adenoma.

Tx: For pts w b/l adrenal hyperplasia: aldosterone antagonists such as sipronolacone, eplerenone)

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2
Q

Diabetic foot ulcer caused by?

A

peripheral sensory neuropathy (microvascular damage is secondary)

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3
Q

Most common cause of hypothyroidism and lab findings?

A

hashimoto thyroditis. High TSH, low T4, anti-TPO

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4
Q

Most common cause of Cushing syndrome

A

Corticosteroids. Second most common is Cushing dz

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5
Q

HTN, hypoK, and metabolic alkalosis

A

Primary hyperaldosteronism (due to Conn syndrome or b/l adrenal hyperplasi)

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6
Q

Which anti-adrenergic (alpha or beta) drugs come first in treating pheochromocytoma?

A

alpha-antagonists first (phenoxybenzamine)

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7
Q

Treatment for central DI

A

DDAVP and free-water restriction

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8
Q

Postop patient with significant pain p/w hyponatremia and normal volume status

A

SIADH 2/2 stress of surgery

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9
Q

DM II w Lactic acidosis. what drug?

A

metformn

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10
Q

Pt with weakness, nausea, vomiting, weight loss, and skin hyperpigmentation. Lab results show HypoNa and HyperK, Tx?

A

Primary adrenal insufficiency (Addison disease). Tx w glucocorticoids, mineralocorticoids, and IV fluids.

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11
Q

Goal HbA1c in Type II DM?

A

Less than 7%

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12
Q

Bone pain, hearing loss, and increased AlkPhos. Dx?

A

Paget disease

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13
Q

Increased insulin-like growth factor-1. Dx?

A

Acromegaly

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14
Q

Classic CAH. What enzyme is deficient?

A

21-OH deficiency. 17-hydroxyprogesterone is elevated. 46, XX baby will show ambiguous genitalia and have hypotension
46, XY may have normal genitalia at birth or enlarged phallus

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15
Q

MEN 1 syndrome

A

3 Ps: pancreas, pituitary, and parathyroid tumors

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16
Q

Men 2A

A

2 Ps: Medullary thyroid cancer, parathyroid tumors, pheochromocytoma,

17
Q

MEN 2B

A

1P: MNoP: Medullary thyroid cancer, Neuromas, Pheochromcyomas

18
Q

4 types of thyroid cancer

A

Papillary (most Popular, Psammoma bodies, Orphan Annie Nuclei, lymphatic spread)
Follicular (hematologic spread)
Medullary (associated with MEN2A/B)
Anaplastic

19
Q

Hypercalcemia causes: CHIMPANZEES

A
Calcium supplementation, Hyperparathyroidism/hyperthyroidism
Iatrogenic - thiazides, parenteral nutrition OR Immobility
Milk-Alkali
Paget Dz of Bone
Adrenal Insufficiency  OR Acromegaly
Neoplasia
Zollinger Ellison Syndrome (MEN1)
Excess Vitamin D
Excess Vitmain A
Sarcoidosis (and TB)
20
Q

SIADH PDT+ Path

A

Too much ADH (can come from posterior pituitary lesion or brain injury) = too much water = hypotonic serum
D: Euvolemic Hyponatremia
Decreased serum Osms
Increased Urine Na and Urine Osms
Tx: H2O restriction, demclocycline or Vaptan

21
Q

Central DI PDT+ Path

A

No ADH production
P: polyuria, polydipsia, NL Blood glucose
D: H2O restrict, then if corrects with desmopressin (DDAVP), then it’s central
T:DDAVP

22
Q

Nephrogenic DI PDT+ Path

A

Kidney resistant to ADH
P: polyuria, polydipsia, NL Blood glucose
D: H2O restrict,
if doesn’t correct with desmopressin (DDAVP), then it’s nephrogenic
T: Gentle diuresis w loop diuretic

23
Q

PDT for Secondary hyperaldosteronism

A
Path: young woman, fibromuscular dysplasia OR old man w renal artery stenosis
P: HTn + hypoK
D: Aldo/Renin<10
Angiogram
Tx: RAS=medical management
Fibromuscular dysplasia=stent
24
Q

Multinodular goiter scan will show?

A

The thyroid scan is now demonstrating an enlarged gland with multiple nodules (“areas”), some avid/hyperfunctioning and other relatively depressed (either not “hyper”-functioning and thus relatively cold or actually cold, most commonly filled with colloid).

25
Q

ca and vit. D levels in sarcoidosis

A

Chronic sarcoidosis
↑ Calcium due to elevated levels of 1,25-(OH)2-vitamin D3
↓ CD4+ T cells: T helper cells are consumed during granuloma formation → CD4+ levels are low in serum and high in bronchoalveolar lavage.