Giant Cell Myocarditis Attributable to Myositis: Therapeutic Management under the Guidance of Serial Endomyocardial Biopsy. A case report

Marina Arai, Yu Kataoka, Y. Tsukamoto, Keiko Ohta-Ogo
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Abstract

Giant cell myocarditis is a fatal disease which could be rapidly progressive if not properly managed. However, the role of immunosuppressive therapy, especially in refractory cases, remains unclear. 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. 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.
肌炎引起的巨细胞心肌炎:心内膜活检指导下的治疗管理。病例报告
巨细胞心肌炎是一种致命疾病,如果处理不当,病情可能会迅速恶化。然而,免疫抑制疗法的作用,尤其是在难治性病例中的作用仍不明确。 一名 76 岁的男子因背部疼痛伴有心肌酶升高而就诊。骨骼肌和心内膜活检发现了巨细胞性肌炎和巨细胞性心肌炎。尽管最初进行了免疫抑制治疗,但心肌酶仍持续升高。通过连续的心内膜活检,可以根据组织学炎症活动情况联合使用泼尼松龙、环孢素和霉酚酸酯治疗。 我们介绍了一例先兆有巨细胞性肌炎的难治性巨细胞性心肌炎病例。虽然心内膜活检是一种有手术并发症风险的方法,但它可以在初始免疫抑制疗法无效时指导巨细胞心肌炎的治疗。
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