X linked agammaglobulinaemia and rheumatoid arthritis.
case_report · Level V
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- Record sourced from PubMed, PMID 15564308.
- Also identified by PMC identifier 1755569.
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Abstract
Much interest has been shown recently in the pathogenic role of B cells in rheumatoid arthritis (RA) owing to the marked clinical responses to anti-CD20 treatment in RA. A patient with X linked agammaglobulinaemia (XLA) presented with an erosive symmetric polyarthritis with histological features of RA, including formation of a destructive pannus. Furthermore, the patient developed subcutaneous nodules that were histologically indistinguishable from rheumatoid nodules. Surprisingly, lymphocytic infiltrates in both the synovium and nodule consisted almost exclusively of CD8+ T cells. Although some peculiar B cell subsets have been described in patients with XLA, no B cell subsets could be demonstrated in synovial tissue or the subcutaneous nodule. This case illustrates that classical RA can develop in the absence of mature B cells.
Medical subject headings
- Agammaglobulinemia
- Arthritis, Rheumatoid
- CD8-Positive T-Lymphocytes
- Genetic Diseases, X-Linked