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Lambert-Eaton Myasthenic Syndrome; Pathogenesis, Diagnosis, and Therapy

机译:Lambert-Eaton重症肌无力综合征;发病机制,诊断和治疗

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Lambert-Eaton Myasthenic Syndrome (LEMS) is a rare disease with a well-characterized pathogenesis. In 50% of the patients, LEMS is a paraneoplastic manifestation and caused by a small cell lung carcinoma (SCLC). Both LEMS patients with SCLC and those without this tumour have in 85% of cases pathogenetic antibodies of very high LEMS specificity against voltage-gated calcium channels (VGCCs) in the cell membrane of the presynaptic motor nerve terminal. Better understanding of LEMS pathogenesis has lead to targeted symptomatic therapy aimed at the neuromuscular junction and to semispecific immuno-suppression. For SCLC LEMS, tumour therapy is essential.
机译:Lambert-Eaton重症肌无力综合症(LEMS)是一种罕见的疾病,其发病机理十分明确。在50%的患者中,LEMS是副肿瘤性表现,由小细胞肺癌(SCLC)引起。患有SCLC的LEMS患者和未患有此肿瘤的LEMS患者,在突触前运动神经末梢的细胞膜中,对电压门控钙通道(VGCC)的LEMS特异性都很高,其中有85%的致病性抗体。对LEMS发病机制的更好理解已导致针对神经肌肉接头的靶向对症治疗和半特异性免疫抑制。对于SCLC LEMS,肿瘤治疗至关重要。

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