Giant Cell Myocarditis in a Patient With a Spondyloarthropathy After a Drug Hypersensitivity Reaction

Abstract A young woman thought to have seronegative rheumatoid arthritis developed Stevens-Johnson syndrome after treatment with sulfasalazine; this resolved with prednisone. Later she was found to be HLA-B27-positive in keeping with a spondyloarthropathy. Soon afterward, she developed clinical myop...

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Veröffentlicht in:Canadian journal of cardiology 2013-09, Vol.29 (9), p.1138.e7-1138.e8
Hauptverfasser: Mitoff, Peter R., MD, Mesana, Thierry G., MD, Mielniczuk, Lisa M., MD, Grenon, Jackie, MSN, Veinot, John P., MD, Cooper, Leslie T., MD, Davies, Ross A., MD
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Sprache:eng
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Zusammenfassung:Abstract A young woman thought to have seronegative rheumatoid arthritis developed Stevens-Johnson syndrome after treatment with sulfasalazine; this resolved with prednisone. Later she was found to be HLA-B27-positive in keeping with a spondyloarthropathy. Soon afterward, she developed clinical myopericarditis and cardiogenic shock that responded initially to methylprednisolone and intravenous immunoglobulin, but recurred. An endomyocardial biopsy demonstrated active myocarditis with a mixed cell composition including rare giant cells, but not enough to classify it as giant cell myocarditis. Heart failure symptoms returned and she eventually required a heart transplant; the explanted heart showed giant cell myocarditis.
ISSN:0828-282X
1916-7075
DOI:10.1016/j.cjca.2012.12.011