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Lambert-Eaton Myasthenic Syndrome Caused by Nivolumab in a Patient with Squamous Cell Lung Cancer

机译:Nivolumab引起鳞状细胞肺癌患者的Lambert-Eaton重症肌无力综合征

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Lambert-Eaton myasthenic syndrome (LEMS) is a representative paraneoplastic neurological syndrome. Recently, nivolumab, an anti-programmed cell death 1 inhibitor, has been approved for advanced non-small-cell lung cancer. Careful attention should be paid to immune-related adverse events (irAEs), including neurotoxicity. We herein report a 73-year-old woman with LEMS that occurred during nivolumab treatment for pulmonary squamous cell carcinoma. After the 20th week of nivolumab, she experienced various neurological symptoms such as ptosis, lower limb weakness, and photophobia. Findings from a nerve conduction study and a positive anti-P/Q-type voltage-gated calcium channel antibody made a diagnosis of LEMS. Pyridostigmine and 3,4-diaminopyridine temporarily improved her symptoms. This was the first case of LEMS as a neurological irAE. LEMS should be considered as a possible neurological irAE.
机译:兰伯特-伊顿肌无力综合症(LEMS)是代表性的副肿瘤性神经系统综合症。最近,抗编程性细胞死亡1抑制剂nivolumab已被批准用于晚期非小细胞肺癌。应特别注意免疫相关的不良事件(irAE),包括神经毒性。我们在此报告了一名73岁的LEMS患者,该患者在肺部鳞状细胞癌的nivolumab治疗期间发生。尼古鲁单抗治疗第20周后,她经历了各种神经系统症状,如上睑下垂,下肢无力和畏光。从神经传导研究和抗P / Q型电压门控钙通道抗体阳性的发现可以诊断LEMS。吡啶斯的明和3,4-二氨基吡啶可暂时改善症状。这是LEMS作为神经性irAE的第一例。应将LEMS视为可能的神经学irAE。

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