Fulminant myocarditis in polymyositis.

K. Yukiiri, K. Mizushige, T. Ueda, T. Nanba, K. Tanimoto, Y. Wada, Y. Takagi, K. Ohmori, M. Kohno
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引用次数: 8

Abstract

Cardiac involvement in patients with polymyositis is usually asymptomatic and associated with a mild clinical course. A female patient with muscle weakness and cardiogenic shock, who was diagnosed with polymyositis and fulminant myocarditis, is described. A large amount of methylprednisolone, in addition to intra-aortic balloon pumping and percutaneous cardiopulmonary support, led to the recovery of her cardiac function. However, a massive cerebral embolism occurred and she died. Postmortem histopathological examination showed necroses of muscles and diffuse invasion of mononuclear cells in both the myocardium and the biceps muscle of her arm. Although the mechanism of cardiac dysfunction is not clear, immunosuppressive therapy was effective for fulminant myocarditis in the present case.
多发性肌炎并发暴发性心肌炎。
多肌炎患者的心脏受累通常无症状,并伴有轻微的临床病程。一位女性患者的肌肉无力和心源性休克,谁被诊断为多肌炎和暴发性心肌炎,是描述。大量甲基强的松龙,加上主动脉内球囊泵送和经皮心肺支持,使其心功能恢复。然而,发生了严重的脑栓塞,她死了。死后组织病理学检查显示,其手臂的心肌和二头肌均有肌肉坏死和单核细胞弥漫性浸润。虽然心功能障碍的机制尚不清楚,但免疫抑制治疗对本例暴发性心肌炎有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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