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General Medicine · Rheumatology: cryoglobulinaemic vasculitis
Sample itemA 55-year-old man with untreated chronic hepatitis C has palpable purpura on the legs, arthralgia and new haematuria with proteinuria. Which laboratory pattern is most expected?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
C. Very low C4 with a positive rheumatoid factor and detectable cryoglobulins
Chronic hepatitis C drives mixed (type II) cryoglobulinaemia, in which a monoclonal IgM with rheumatoid factor activity binds polyclonal IgG, forming immune complexes that fix complement through the classical pathway. C4 is typically markedly low, and the typical manifestations are purpura, arthralgia, neuropathy and membranoproliferative glomerulonephritis. Treatment is antiviral therapy, with rituximab for severe vasculitis.
Option by option
A. Raised C4 with positive anti-CCP antibodies
Anti-CCP marks rheumatoid arthritis and a raised C4 would not accompany immune complex consumption.
B. Normal complement levels with positive PR3-ANCA
PR3-ANCA with normal complement describes granulomatosis with polyangiitis, a pauci-immune vasculitis.
C. Very low C4 with a positive rheumatoid factor and detectable cryoglobulins (correct)
Correct. Classical pathway consumption with an IgM rheumatoid factor characterises hepatitis C cryoglobulinaemia.
D. Low C3 with high-titre anti-dsDNA antibodies
Low C3 with anti-dsDNA suggests lupus nephritis rather than a virus-driven cryoglobulinaemic syndrome.
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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