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Microbiology · Immunology: scleroderma antibodies
Sample itemA 45-year-old woman has had Raynaud phenomenon for ten years, with subcutaneous calcinosis, facial telangiectasia and sclerodactyly. Skin thickening is limited to the fingers and face. There is no interstitial lung disease or renal crisis. Which autoantibody is most likely to be found?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
A. Anti-centromere antibody
Limited cutaneous systemic sclerosis (the CREST pattern) is strongly associated with anti-centromere antibodies and carries a risk of pulmonary arterial hypertension. Diffuse disease is linked to anti-topoisomerase I, which predicts interstitial lung disease, and to anti-RNA polymerase III, which predicts scleroderma renal crisis.
Option by option
A. Anti-centromere antibody (correct)
Anti-centromere antibody is the classic marker of limited cutaneous disease with a long Raynaud history.
B. Anti-Jo-1 antibody
Anti-Jo-1 is a marker of the antisynthetase syndrome with myositis and lung disease, not sclerosis.
C. Anti-RNA polymerase III antibody
Anti-RNA polymerase III is associated with rapidly progressive diffuse disease and renal crisis, which are absent here.
D. Anti-topoisomerase I (anti-Scl-70) antibody
Anti-Scl-70 is associated with diffuse skin involvement and pulmonary fibrosis, which are absent here.
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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