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General Medicine · Rheumatology: Felty syndrome
Sample itemA 58-year-old woman with long-standing seropositive rheumatoid arthritis with deformed hands, who takes only NSAIDs, has recurrent skin and chest infections. Examination shows splenomegaly, and her neutrophil count is 0.9 x 10^9/L with normal haemoglobin and platelets. What is the most likely diagnosis?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
C. Felty syndrome
Felty syndrome is the triad of rheumatoid arthritis, splenomegaly and neutropenia, occurring in severe, seropositive, long-standing disease, often with HLA-DR4. Neutropenia arises from immune destruction, splenic sequestration and marrow suppression, causing recurrent infections. Disease-modifying therapy, particularly methotrexate, is the mainstay, with splenectomy for refractory cases.
Option by option
A. Caplan syndrome
Caplan syndrome is rheumatoid arthritis with pneumoconiosis and lung nodules, with no splenomegaly or neutropenia.
B. Sjogren syndrome with lymphoma
Sjogren syndrome with lymphoma is possible, but nothing here points to sicca symptoms or a mass, and the triad fits better with Felty.
C. Felty syndrome (correct)
Correct. Rheumatoid arthritis with splenomegaly and neutropenia defines Felty syndrome.
D. Systemic lupus erythematosus
Lupus causes cytopenias but is not characterised by deforming seropositive arthritis with splenomegaly in this pattern.
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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