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一名小细胞肺癌患者的兰伯特-伊顿肌无力综合征

Lambert-eaton myasthenic syndrome in a patient with small-cell lung cancer.

作者信息

Wang Shulian, Bruzzi John, Rodriguez-Garza Veronica P, Komaki Ritsuko R

机构信息

Department of Radiation Oncology, Cancer Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China.

出版信息

Clin Lung Cancer. 2006 Jan;7(4):282-4. doi: 10.3816/CLC.2006.n.008.

Abstract

Lambert-Eaton myasthenic syndrome (LEMS), an autoimmune neuromuscular disorder, often has underlying small-cell lung cancer (SCLC). Thorough search for SCLC in patients with LEMS can result in early detection of limited-stage SCLC, one quarter of which can be successfully treated with chemotherapy and radiation therapy. To elucidate the pathogenesis, diagnosis, treatment, and prognosis of patients with SCLC and LEMS, we present a 51-year-old man who was diagnosed with LEMS and limited-stage SCLC after an 18-month history of weakness in the lower extremities. The patient exhibited a complete response in lung tumors and a resolution in LEMS symptoms after chemotherapy and radiation therapy.

摘要

兰伯特-伊顿肌无力综合征(LEMS)是一种自身免疫性神经肌肉疾病,常伴有潜在的小细胞肺癌(SCLC)。对LEMS患者进行全面的SCLC筛查可实现局限期SCLC的早期发现,其中四分之一的患者可通过化疗和放疗成功治疗。为阐明SCLC合并LEMS患者的发病机制、诊断、治疗及预后,我们报告一名51岁男性,其在出现下肢无力18个月后被诊断为LEMS合并局限期SCLC。该患者在接受化疗和放疗后,肺部肿瘤完全缓解,LEMS症状消失。

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