Lee Jae-Hyeok, Shin Jin-Hong, Kim Dae-Seong, Jung Dae Soo, Park Kyu-Hyun, Lee Min-Ki, Kim Jee-Yeon
Department of Neurology, College of Medicine, Pusan National University, Busan, Korea.
J Korean Med Sci. 2004 Oct;19(5):753-5. doi: 10.3346/jkms.2004.19.5.753.
The Lambert-Eaton myasthenic syndrome (LEMS) is typically recognized as a paraneoplastic syndrome associated with a small cell lung carcinoma (SCLC), whereas LEMS with other neuroendocrine lung tumors, including carcinoids or large cell lung carcinoma, are highly unusual. Here, we report a rare case of LEMS with atypical bronchopulmonary carcinoid tumor: a 65-yr-old man presented with progressive leg weakness and a diagnosis of LEMS was made by serial repetitive nerve stimulation test. Chest CT revealed a lung nodule with enlargement of paratracheal lymph nodes, and surgically resected lesion showed pathological features of atypical carcinoid tumor. We concluded that LEMS could be associated with rare pulmonary neuroendocrine tumor other than SCLC, which necessitates pathologic confirmation followed by aggressive treatment for optimal management in these rare cases.
兰伯特-伊顿肌无力综合征(LEMS)通常被认为是一种与小细胞肺癌(SCLC)相关的副肿瘤综合征,而LEMS与其他神经内分泌性肺肿瘤(包括类癌或大细胞肺癌)相关的情况则极为罕见。在此,我们报告一例罕见的LEMS合并非典型支气管肺类癌肿瘤的病例:一名65岁男性出现进行性腿部无力,通过系列重复神经刺激试验确诊为LEMS。胸部CT显示肺部有结节伴气管旁淋巴结肿大,手术切除的病变显示为非典型类癌肿瘤的病理特征。我们得出结论,LEMS可能与SCLC以外的罕见肺神经内分泌肿瘤相关,在这些罕见病例中,需要进行病理确诊,随后积极治疗以实现最佳管理。