CTD: Lupus. Lecture review Qs Flashcards

1
Q

what medication unmasks true SLE

A

penicillamine

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2
Q

medications implicated in drug-induced SLE

A
MMC is HIP
Minocycline
Methyldopa
Chlorpromazine
Hydralazine
Isoniazid
Procainamide
Phenytoin
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3
Q

immunologic markers for renal disease in SLE

A

anti-dsDNA

anti-C1q

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4
Q

what is Sneddon syndrome

A

livedo reticularis, cerebrovascular infarcts and htn (may have SLE)

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5
Q

treatment of bullous SLE

A

dapsone

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6
Q

what does bullous SLE attack? HLA associated?

A

type 7 collagen

HLA-DR2

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7
Q

what does ASAP syndrome stand for and what is it

A

Acute Syndrome of Apoptotic Pan-Epidermolysis

TEN-like presentation in SLE

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8
Q

what is Rowell syndrome

A

EM-like lesions in lupus

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9
Q

11 criteria for SLE

A
SOAP BRAIN MD
Serositis
Oral ulcerations
Arthritis
Pleuritis
Blood abnormalities
Renal abnormalities
ANA +
Immunologic abnormalities
Neurologic abnromalities
Malar rash
Discoid lesions
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10
Q

who does SLE affect

A

young-middle age women (6:1) and African Americans (4:1)

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11
Q

clinical presentation of neonatal lupus

A

periocular edema and erythema (racoon’s eyes)

appear in first few weeks of life

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12
Q

associations in neonatal lupus

A

congenital heart block, thrombocytopenia, hepatobiliary ds

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13
Q

if only __ ab is present in neonatal lupus, then there is no risk of heart block

A

U1RNP

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14
Q

what medication can lower the risk of neonatal lupus to 7% if initiated prior to 10 wks gestation

A

hydroxychloroquine

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15
Q

what is the risk that a second child will have neonatal lupus

A

25%

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16
Q

neonatal lupus is due to transferring __ ab across the placenta

A

anti-Ro/SSa

17
Q

most important treatment for DLE and SCLE

A

sunscreen

18
Q

30% of SCLE cases are drug-induced. what drugs?

A
HANG NAIL
HCTZ
ACE-I and Antihistamines
NSAIDs
Griseofulvin
Nifedipine
Anticonvulsants
Interferon
Lamisil
19
Q

clinical description of SCLE

A

sun exposed scaly, annular plaques

20
Q

10-15% of SCLE pts develop internal symptoms. what are they?

A

arthritis, leukopenia, renal, CNS, vascular complications

21
Q

antibody in 70% SCLE pts

A

anti Ro/SSa

22
Q

percentage of pts with positive ANA in SCLE

A

80%

23
Q

percentage of pts with SCLE that will get SLE

A

30%

24
Q

anatomical area spared in lupus panniculitis

A

distal extremities

25
Q

percentage of pts with tumid lupus that will have overlying DLE

A

30%

26
Q

percentage of pts with tumid lupus that will develop SLE

A

50%

27
Q

tumid lupus overlaps with what entities

A

REM (reticular erythematous mucinosis)

jessner’s lymphocytic infiltrate

28
Q

how often does tumid lupus have overlying epidermal involvement

A

never

29
Q

mutation in familial form of chilblain lupus

A

TREX1

30
Q

LE-LP overlap syndrome most commonly affects what area

A

palmoplantar

also oral with scarring alopecia

31
Q

percentage of pts with DLE that have +DIF

A

75%

32
Q

percentage of SLE pts with DLE

A

25%

33
Q

percentage of DLE pts that develop SLE

A

5-15%

34
Q

childhood DLE has higher progression to?

A

SLE

35
Q

what do you need to worry about in long-standing DLE

A

SCC

36
Q

most common location DLE

A

above the neck - scalp and concha

37
Q

langue au chat refers to

A

cat’s tongue - follicular carpet tack like plugging in DLE

38
Q

forms of chronic cutaneous lupus

A

discoid, hypertrophic, LE-LP overlap, chilblain, tumid, lupus panniculitis

39
Q

other name for Sjogren syndrome

A

Sicca syndrome, Mikulicz ds