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表现为多发性肌炎的恶性胸腺瘤和重症肌无力:一例报告

Malignant thymoma and myasthenia gravis presenting as polymyositis: a case report.

作者信息

Lee Anh B, Thurston R Scott

机构信息

Louisiana State University Health Sciences Center, Department of Surgery, New Orleans, USA.

出版信息

J La State Med Soc. 2008 Sep-Oct;160(5):286-8.

Abstract

Polymyositis revealing myasthenia gravis and malignant thymoma: a case report. The increased frequency of thymoma associated with autoimmune diseases has been well documented in the literature. However the association of polymyositis (PM) and myasthenia gravis (MG) revealing a malignant thymoma is rare. We report a case of a gentleman whose presenting symptoms were those of polymyositis.

摘要

多发性肌炎并发重症肌无力及恶性胸腺瘤

一例报告。文献中已充分记载了胸腺瘤与自身免疫性疾病相关的频率增加。然而,多发性肌炎(PM)与重症肌无力(MG)并发恶性胸腺瘤的情况较为罕见。我们报告一例男性患者,其首发症状为多发性肌炎症状。

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