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 |
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Format: | Artikel |
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. |
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ISSN: | 0828-282X 1916-7075 |
DOI: | 10.1016/j.cjca.2012.12.011 |