endo Flashcards

1
Q

increased cortisol, decreased ACTH and B/L adrenal atrophy?

A

exogenous steroid use –> Cushing syndrome

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2
Q

increased cortisol, decreased ACTH, unilateral adrenal atrophy?

A

1ary adrenal adenoma, hyperplasia, or carcinoma

** can also present with pseudohyperaldo

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3
Q

increased cortisol, increased ACTH, B/L adrenal hyperplasia?

A

ACTH-secreting adenoma = Cushing disease

or ectopic ACTH - e.g. paraneoplastic

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4
Q

diagnostic method for hypercortisolism?

A

1) serum ACTH - if low, adrenal tumor –> MRI
2) if high –> high dose dex suppression and CRH stim tests

    • adequate dex suppression and increase in ACTH/cortisol with CRH –> Cushing disease
    • no suppression and no change in ACTH/cortisol with CRH –> ectopic ACTH
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5
Q

weakness, fatigue, orthostasis, muscle aches, weight loss, GI disturbances, sugar/salt cravings?

A

adrenal insufficiency

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6
Q

dx of adrenal insufficiency?

A

serum electrolytes, serum cortisol and ACHT, ACTH stim test

** metyrapone stim test (blocks 11deoxycortisol –> cortisol) - normal response = decreased cortisol and increased ACTH; if ACTH remains low then dx = adrenal insuff

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7
Q

hypotension, hyperkalemia, metabolic acidosis, skin and mucosal hyperpigmentation?

A

primary adrenal insufficiency
(MCC in West = autoimmune)

** hyperpigmentation 2/2 MSH = byproduct of increased ACTH production

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8
Q

Waterhouse Friedrichsen?

A

acute 1ary adrenal insufficiency from adrenal hemorrhage

2/2 septicemia (usually N meningitidis), DIC, endotoxic shock

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9
Q

adrenal insufficiency w/o hyperpigmentation or hyperkalemia?

A

secondary adrenal insufficiency
from decreased pituitary ACTH secretion
aldosterone preserved

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10
Q

kid with abdominal distension and firm irregular mass that crosses midline?

A

neuroblastoma - adrenal medulla (from neural crest cells)
HVA and MVA in urine
bombesin and neuron specific enolase +
overexpression of N-myc oncogene

** Homer-Wright rosettes on biopsy

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11
Q

dancing eyes, dancing feet?

A

opsoclonus-myoclonus

seen in neuroblastoma

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12
Q

rule of 10s in pheo?

A
10% malignant
10% B/L
10% extra adrenal
10% calcify
10% kids
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13
Q

what cells do pheos come from?

A

chromaffin cells - neural crest origin

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14
Q

changes in cholesterol in thyroid dz?

A

hypothyroid –> increased cholesterol 2/2 decreased LDL receptor expression
hyperthyroid –> decreased cholesterol 2/2 increased LDL receptor expression

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15
Q

thyroid biopsy: Hurthle cells, lymphoid aggregate with germinal centers?

A

Hashimoto
HLA DR5 assoc
thyroid non-tender

** increased risk of NHL

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16
Q

pot bellied baby with pale skin, puffy face, protruding umbilicus and tongue?

A

congenital hypothyroidism = cretinism

2/2 maternal hypothyroidism, thyroid agenesis, thyroid dysgenesis, iodine deficiency, dyshormogenetic goiter
MCC in US = thyroid dysgenesis

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17
Q

tender thyroid, jaw pain following flu-like illness?

A

subacute thyroiditis = de Quervain
increased ESR

** biopsy: granulomatous inflammation

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18
Q

fixed, rock hard, painless goiter?

A

Riedel thyroiditis
replacement of thyroid by fibrous tissue; may extend to local structures

** 2/2 IgG4-related dz - e.g. autoimmune pancreatitis, retroperitoneal fibrosis, noninfectious aortitis

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19
Q

Wolff-Chaikoff effect?

A

downregulation of thyroid gland in response to increased iodide

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20
Q

pathogenesis of toxic multinodular goiter?

A

mutation of TSH receptor –> hyperfunctioning follicular cells

21
Q

cause of death in thyroid storm?

A

tachyarrhythmia

22
Q

tx of thyroid storm?

A

BBs
PTU
steroids

23
Q

Jod Basedow phenomenon?

A

thyrotoxicosis following iodine repletion in pt with iodine-deficiency goiter

24
Q

thyroid biopsy: Orphan Annie eyes, psammoma bodies, nuclear grooves?

A

papillary thyroid carcinoma - MC, good prog
increased risk with RET and BRAF mutations, hx of childhood irradiation

** lymphatic invasion common

25
thyroid biopsy: uniform follicles, thyroid capsule invasion?
follicular carcinoma | good prognosis
26
thyroid biopsy: sheets of cells in amyloid stroma?
medullary carcinoma - from parafollicular "C cells" assoc with MEN2A and 2B produces calcitonin ** hematogenous spread common
27
thyroid cancer in older patients?
undifferentiated/anaplastic ** invades local structures
28
hypocalcemia, shortened 4th/5th digits, short stature?
pseudohypoparathyroidism = Albright hereditary osteodystrophy AD kidney unresponsive to PTH
29
familial hypocalciuric hypercalcemia?
defective Ca-sensing rcptr on parathyroid cells | --> mild hypercalcemia, normal to increased PTH levels
30
MCC of 1ary hyperparathyroidism?
parathyroid adenoma or hyperplasia
31
findings in 1ary hyperparathyroidism?
``` hyperCa hypercalciuria --> stones hypoPh increased PTH increased ALP increased cAMP in urine ```
32
findings in 2ary hyperparathyroidism?
hypoCa hyperPh increased PTH increased ALP
33
cancer risk in acromegaly?
increased risk of colorectal polyps/cancer
34
MCC of death in acromegaly?
HF
35
causes of nephrogenic DI?
hereditary - ADH receptor mutation hypercalcemia lithium demeclocycline (ADH antag)
36
tx of central DI?
intranasal desmopressin acetate
37
tx of nephrogenic DI?
HCTZ indomethacin amiloride
38
causes of SIADH?
paraneoplastic - SCLC CNS/trauma pulmonary disease cyclophosphamide
39
tx of SIADH?
``` fluid restriction IV hypertonic saline (be caaaaareful!) ADH antag (conivaptan, tolvaptan, demeclocyline) ```
40
empty sella syndrome?
atrophy or compression of pituitary | common in obese women
41
MCC of death in diabetes?
MI
42
DM1 vs DM2: genetic predisposition?
DM1 - weaker | DM2 - stronger
43
why don't type 2 DM pts usually get DKA?
endogenous insulin usually prevents lipolysis
44
dermatitis, hyperglycemia, DVTs, depression?
glucagonoma | - necrolytic migratory erythema
45
recurrent diarrhea, cutaneous flushing, asthmatic wheezing?
carcinoid syndrome - MC malignancy in SI only get sx if mets - if in GI tract, 5HT metabolized in liver dx: 5HIAA in urine, niacin deficiency ** causes R sided valvular heart disease
46
MEN 1?
MEN1 mutation - menin = tumor suppressor parathyroid tumors pituitary tumors pancreatic endocrine tumors (Zollinger Ellison, insulinoma, VIPoma, glucagonoma)
47
MEN 2A?
RET mutation (tyr kinase) parathyroid hyperplasia pheo medullary thyroid carcinoma
48
MEN 2B?
RET mutation (tyr kinase) pheo medullary thyroid carcinoma marfanoid habitus mucosal neuromas - oral/intestinal