Cutaneous Manifestations of Systemic Disease Flashcards

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1
Q

cutaneous findings of AL amyloidosis

A

macroglossia (can lead to tongue trauma), pinch purpura, waxy thickening, nodules/ plaques in periorbital region

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2
Q

dx of AL amyloid

A

biopsy needed- apple green on congro red in papillary dermis

serum and urine electrophoresis can detect light chains

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3
Q

tx of amyloid

A

treat plasma cell dyscrasia

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4
Q

main systems affected by sacroid

A

lungs and skin, but can be any system

mostly AA and female

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5
Q

biopsy of sarcoid

A

non caseating granulomas

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6
Q

skin finding of sarcoid

A

symmetric red brown papules/ plaques

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7
Q

logfrens syndrome

A

sarcoid w/ erythema nodosum, hilar adenopathy, fever

better px

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8
Q

what lesion has predilection of scars and and tatoos

A

sarcoid

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9
Q

tx for sarcoid

A

should remit, no cure

CS, antimalarials, minocycline, immunomodulators help

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10
Q

describe necrobiosis lipoidica, tx

A

necrotiing skin w/ DM

primarily young and middle aged adults

topical steroids firts line

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11
Q

skin findings of necrobiosis lipoidica

A

yellow brown atrophic telangiectatic plaques w/ elevated rim,

usually pretibial, flame like appearance

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12
Q

sweets syndrome epi

A

aka acute febrile neutrophilic dermatosis

usually female, 30-60, acute onset

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13
Q

clin pres of sweet syndrome

A

fever, malaise, abrupt erythematous palques w/ some vesiculation (usualy on head and neck but can be anywhere)

elevated WBC and pmn count

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14
Q

etiology of sweets

A

half idiopathic, half trigger

URIs like strep, malignancy (AML), chronic inflammatory

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15
Q

tx of sweets

A

tx underlying infection, systemic CS causes rapid improvement

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16
Q

most common form of panniculitis

A

erythema nodosum- tender nodules on anterior lower legs, w/o ulceration

17
Q

etiology of erythema nodosum

A

half idopathic, half trigger

delayed hypersensitivity: infections, abx, OCP, pregnancy

18
Q

EN epi

A

usually women, 20-30

19
Q

systemic sx of erythema nodosum

A

arthritis, arthralgia, malaise, fever

20
Q

tx of EN

A

NSAIDs, underlying disease

21
Q

assoc of calcific uremic arteriolopathy

A

aka calciphylaxis

assoc w/ ESRD

22
Q

clin pres of calciphylaxis

A

starts w/ painful sub q nodules and plaques

forms chronic painful ulcers, typically lower extremities an dtrunk

23
Q

dx of calciphylaxis

A

biopsy shows arteriolar calcification

24
Q

tx of calciphylaxis

A

surgical debridement

meds inconsistent, sodium thiosulfate most common

need kidney transplant

stop vit D, Ca, warfarin

low 1 yr survival