[A case of small cell lung cancer that presented with paraneoplastic syndrome].

Masatoshi Wakatsuki, Kiyoshi Matsuo, Hiroe Kayatani, Keiichi Fujiwara, Toshiro Yonei, Toshio Sato
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Abstract

A 65-year-old man had suffered from systemic erythema from November 2008 and had noticed gradually progressing weakness in the upper and lower limbs. He received medical treatment in another hospital but his symptoms did not improve. He was admitted to our hospital for treatment of diabetes in June 2009, and his chest X-ray images and CT scans showed a mass shadow in the right upper lobe with hilar and mediastinal lymphadenopathy. We performed bronchoscopy, and diagnosed small cell lung cancer (T2N2M1, stage IV). However, he had hand grip weakness and continuing upper and lower limb muscle weakness, and therefore electromyography was performed, which showed the presence of waxing in the right leg. Subsequently, a diagnosis of Lambert-Eaton myasthenic syndrome was made. As he also showed ataxia of the left lower extremity, we also diagnosed paraneoplastic cerebellar degeneration. We gave the patient chemotherapy consisting of carboplatin and etoposide which resulted in the disappearance of his waxing, and his grip strength and erythema immediately improved with regression of the tumor after 1 course of chemotherapy. We report a case of small cell lung cancer associated with Lambert-Eaton myasthenic syndrome, paraneoplastic cerebellar degeneration and erythema which presented as paraneoplastic syndrome, which improved with chemotherapy.

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[以副肿瘤综合征为表现的小细胞肺癌一例]。
65岁男性,自2008年11月起患有全身性红斑,上肢和下肢逐渐虚弱。他在另一家医院接受了治疗,但他的症状没有改善。2009年6月因糖尿病入院,胸部x线及CT示右上肺叶肿块影伴肺门及纵隔淋巴结病变。我们进行了支气管镜检查,诊断为小细胞肺癌(T2N2M1, IV期)。然而,患者手部握力无力,上肢和下肢肌肉持续无力,因此进行了肌电图检查,显示右腿有蜡样。随后,诊断为兰伯特-伊顿肌无力综合征。由于他也表现出左下肢共济失调,我们也诊断出副肿瘤小脑变性。我们给予患者卡铂加依托泊苷的化疗,使其脱蜡消失,化疗1个疗程后,其握力和红斑立即改善,肿瘤消退。我们报告一例小细胞肺癌合并兰伯特-伊顿肌无力综合征,副肿瘤小脑变性和红斑,表现为副肿瘤综合征,化疗后好转。
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