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Pathology · Vasculitis: eosinophilic granulomatosis with polyangiitis
Sample itemA 38-year-old man with long-standing asthma develops mononeuritis multiplex, a peripheral eosinophil count of 2,500 per microlitre and palpable purpura. Which antibody is most likely to be present?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
A. p-ANCA directed against myeloperoxidase
Eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome) is a small-vessel vasculitis with asthma, eosinophilia and extravascular granulomas, and about 40% are p-ANCA (MPO) positive. Biopsy shows eosinophil-rich necrotising vasculitis. Granulomatosis with polyangiitis typically has c-ANCA.
Option by option
A. p-ANCA directed against myeloperoxidase (correct)
MPO-directed p-ANCA is found in a proportion of patients with this eosinophil-rich vasculitis.
B. c-ANCA directed against proteinase 3
c-ANCA with PR3 specificity is typical of granulomatosis with polyangiitis, without asthma-driven eosinophilia.
C. Anti-dsDNA antibody
Anti-dsDNA is a marker of lupus.
D. Anti-GBM antibody
Anti-GBM antibody causes Goodpasture 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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