Vasculitides and Vaso-occlusive diseases Flashcards

1
Q

what are the 4 CSVV

A

Henoch–Schönlein purpura
Acute hemorrhagic edema of infancy
Urticarial vasculitis
Erythema elevatum diutinum

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2
Q

what drugs can cuase CSVV

A

NSAIDs
COX-2 inhibitors
PCNs
quinolones

(also, ACEi, allopurinol, lasix)

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3
Q

how long after exposure to infection or drug does CSVV appear?

A

7-10 days

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4
Q

describe appearance of CSVV

A

palpable purpuric to erythematous papules, vesicles, and macules on lower extremities/dependent areas

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5
Q

urticaria that lasts > 24 hrs

A

urticarial vasculitis

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6
Q

labs in urticarial vasculitis

A

** majority w/o these findings (75%)
low complement levels
anti-C1q Ab

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7
Q

what is Schnitzerler’s syndrome

A

uritcarial vasculitis with monoclonal IgM gammopathy with at least 2 of the following

  • fever
  • arthralgias
  • LAD
  • HSM
  • elevated ESR
  • leukocytosis
  • bone pain/abnormality
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8
Q

when you see urticarial vasculitis, think about

A
autoimmune connective tissue disease (SLE)
infection (HBV, HCV, EBV)
serum sickness 
malignancy 
meds (KI, NSAIDs, fluoxetine)
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9
Q

treatment of urticarial vasculitis

A

anti-histamines, NSAIDs, cholchicine, dapsone, antimalarials, oral steroids

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10
Q

sites of HSP lesions

A

lower ext and butt

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11
Q

other findings you can see with HSP

A

abdominal pain (colicky), GI bleeding, vomiting
arthritis
hematuria
**usu follows URI

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12
Q

histology + DIF of HSP

A
LCV
perivascular IgA (and C3 and fibrin)
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13
Q

% HSP pts that can develop permanent renal dz

A

2%

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14
Q

describe lesions on EED

A

red, violaceous, brown papules and plques on extensor surfaces

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15
Q

what is EED a/w

A

autoimmune dz
infx (hemolytic strep, HBV, HIV)
IBD
IgA monoclonal gammopathy

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16
Q

treatment of EED

A

dapsone

17
Q

what does EED stand for

A

erythema elevatum diutinum

18
Q

describe lesions of granuloma faciale

A

smooth violaceous to re-brown plaque on face, usu solitary

19
Q

tx for granuloma faciale

A

ILK, dapsone, tacrolimus

* often tx resistant