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胸腺瘤全切术后迟发性重症肌无力:2例报告

Late onset of myasthenia gravis after total resection of thymoma: report of two cases.

作者信息

Mineo T C, Biancari F, D'Andrea V

机构信息

Department of Thoracic Surgery, University Tor Vergata, Rome, Italy.

出版信息

J Cardiovasc Surg (Torino). 1996 Oct;37(5):531-3.

PMID:8941699
Abstract

The authors report two patients presenting myasthenia gravis, respectively, 4 years and 2 months, and 6 years and 7 months after total resection of thymoma. Computed tomographic scan and magnetic resonance imaging did not show any signs of recurrent or metastatic thymoma. Pyridostigmine bromide was successfully administered in both patients. The late onset of autoimmune disorders should be kept in mind as possible and, sometimes, fatal complications of surgical treatment for thymoma. In all cases, recurrent or metastatic thymoma should be ruled out because reoperation may be effective even in the treatment of myasthenia gravis.

摘要

作者报告了两名分别在胸腺瘤全切术后4年2个月和6年7个月出现重症肌无力的患者。计算机断层扫描和磁共振成像未显示复发性或转移性胸腺瘤的任何迹象。两名患者均成功使用了溴吡斯的明。应牢记自身免疫性疾病的迟发性可能是胸腺瘤手术治疗的致命并发症。在所有病例中,都应排除复发性或转移性胸腺瘤,因为再次手术甚至可能对重症肌无力的治疗有效。

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