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General Medicine · Rheumatology: IgA vasculitis
Sample itemA 20-year-old develops palpable purpura on the legs, colicky abdominal pain, arthralgia and haematuria after an upper respiratory infection. What does skin or renal biopsy immunofluorescence show?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
D. Predominant IgA deposition in vessel walls
IgA vasculitis (Henoch-Schonlein purpura) is a small-vessel leukocytoclastic vasculitis with IgA-dominant immune deposits. It presents with palpable purpura, abdominal pain, arthritis and nephritis. Most cases resolve spontaneously.
Option by option
A. Deposits of cryoglobulins only
Cryoglobulinaemic vasculitis involves hepatitis C and mixed cryoglobulins, not this picture.
B. Negative immunofluorescence (pauci-immune)
Pauci-immune pattern characterises ANCA-associated vasculitis.
C. Linear IgG along the basement membrane
Linear IgG is seen in anti-GBM disease.
D. Predominant IgA deposition in vessel walls (correct)
Correct. IgA-dominant deposits define the disease.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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