Endocrinologie Flashcards

1
Q

The most common cause of hypothyroidism

A

Hashimoto thyroiditis

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2
Q

Lab findings in Hashimoto thyroiditis

A

High TSH, low T4 antibodies to thyroid peroxidase (TPO)

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3
Q

Exophtalmos, pretibial myxedema, an lowered TSH

A

Graves disease

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4
Q

The most common cause of Cushin syndrome

A

Iatrogenic corticosteroid administration. The second most common cause is Cushing desease

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5
Q

A patient post-thyroidectomiy presents with signs of hypocalcemia and raised phophorus

A

Hypoparathyroidism (iatrogenic)

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6
Q

Stones, bones, groans, psychiatric overtones

A

Signs and symptoms of hypercalcemia

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7
Q

Hypertension, hypokalemia, and metabolic alkalosis

A

1° hyperaldosteronism (due to Conn syndrome or bilateral adrenal hyperplasia)

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8
Q

A patient presents with tachycardia, wild swings in BP, headache, diaphoresis, altered mental status, and a sense of panic

A

Pheochromocytoma

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9
Q

Which should be used first in treating pheocrhomocytoma, alfa or beta-antagonists

A

alfa-antagonists (phenoxybenzamine)

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10
Q

A patient with a history of lithium use presents with copious amounts of dilute urine

A

nephrogenic diabetes insipidus (DI)

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11
Q

Treatment of central DI

A

Administration of DDAVP and free-water restriction

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12
Q

A postoperative patient with siginificant pain presents with hyponatremia and normal volume status

A

Syndrome of inappropriate antidiuretic hormone (SIADH) due to stress

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13
Q

An antidiabetic agent associated with lactic acidosis

A

Metformin

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14
Q

A patient presents wirh weakness, nausea, vomiting, weight loss, and new skin pigmentation. Lab results show hyponatremia and hyperkalemia. Treatment?

A

1° adrenal insufficiency (Addiso disease). Treat mith glucoqcorticoids, mineralocorticoids, en IV fluids.

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15
Q

Goal HbA1c for a patient with diabetes mellitus (DM)

A

<7.0%

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16
Q

Treatment of diabetic ketoacidosis (DKA)

A

Fluids, insulin, and electrolyte repletion (eg, K+)

17
Q

Bone pain, hearing loss, raise alkaline phosphatase

A

paget disease

18
Q

raised IGF-1

A

Acromegaly

19
Q

Galactorrhea, amenorrhea, bitemporal hemianopia

A

prolactinoma

20
Q

raised serum 17-hydroxyprogesterone

A

congenital adrenal hyperplasia (21-hydroxylase deficiency)

21
Q

pancreas pituitary parathyroid tumors

A

multiple endrocrine neoplasia type 1 (MEN 1)