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Chronic graft-versus-host disease (CGVHD),* a multisystemic syndrome that develops 80–400 days after allogenic marrow transplantation, affects 25–45% of long-term survivors (1, 2). With early medical treatment using prednisone with either azathioprine and/or cyclosporine, scleroderma and joint contractures now rarely occur. Nevertheless, a small proportion of patients will eventually develop dermal thickening, joint contractures, and sicca syndrome (3), which may be resistant to therapy with standard immunosuppressive agents (4).
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Socié et al. (1990) studied this question.
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