Giant cell myocarditis attributable to myositis: therapeutic management under the guidance of serial endomyocardial biopsy—a case report

Author:

Arai Marina123ORCID,Kataoka Yu1ORCID,Tsukamoto Yasumasa2ORCID,Ohta-Ogo Keiko4ORCID

Affiliation:

1. Department of Cardiovascular Medicine, National Cerebral and Cardiovascular Center , 6-1 Kishibeshinmachi, Suita, Osaka 564-8565 , Japan

2. Department of Transplant Medicine, National Cerebral and Cardiovascular Center , Suita , Japan

3. Department of Cardiovascular Medicine, Graduate School of Medicine, Tohoku University , Sendai , Japan

4. Department of Pathology, National Cerebral and Cardiovascular Center , Suita , Japan

Abstract

Abstract Background Giant cell myocarditis is a fatal disease that could be rapidly progressive if not properly managed. However, the role of immunosuppressive therapy, especially in refractory cases, remains unclear. Case summary A 76-year-old man presented with back pain with elevated cardiac enzymes. Skeletal muscle and endomyocardial biopsies revealed giant cell myositis and giant cell myocarditis. Despite the initial immunosuppressive therapy, cardiac enzymes continued to rise. Serial endomyocardial biopsies enabled combination treatment of prednisolone, cyclosporine, and mycophenolate mofetil according to histological inflammatory activity. Discussion We presented a case of refractory giant cell myocarditis preceded by giant cell myositis. While endomyocardial biopsy is an approach with risk of procedural complications, it can guide giant cell myocarditis management when the initial immunosuppressive therapy is ineffective.

Publisher

Oxford University Press (OUP)

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1. Ciclosporin/Methylprednisolone;Reactions Weekly;2024-08-10

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