Lambert-Eaton Syndrome

The Association of the Lambert-Eaton Myasthenic Syndrome with Carcinoma

Lambert-Eaton肌无力综合征与癌

Lambert-Eaton syndrome in patients with small cell lung cancer

小细胞肺癌合并Lambert-Eaton综合征

Carcinomatous Lambert-Eaton Myasthenic Syndrome: Clinical and Electrophysiological Study of 4 Cases

癌性Lambert-Eaton肌无力综合征四例临床及电生理研究

Lambert-Eaton myasthenic syndrome has a more progressive course in patients with lung cancer

肺癌患者Lambert-Eaton肌无力综合征的病程进展更快

Objective To report the clinical features of myasthenia gravis ( MG) combined with Lambert-Eaton myasthenic syndrome ( LEMS).

目的探讨重症肌无力（MG）合并Lambert Eaton肌无力综合征（LEMS）的临床特点。

Associated autoimmune diseases in patients with the Lambert-Eaton myasthenic syndrome and their families

与Lambert-Eaton肌无力综合征患者及其家庭成员相关的自身免疫性疾病

Its chief characteristics is on repetitive nerve stimulation with 5-50 frequencies. The amplitude increases progressively. It requires making differential diagnosis to Lambert-Eaton syndrome.

主要特点是用每秒5～50次连续电刺激神经，诱发肌肉动作电位波幅渐增，用此可协助确定肉毒中毒的诊断，但需和Lambert-Eaton综合征鉴别。

Objective To investigate the diagnosis of Lambert-Eaton syndrome and the relations between it and primary tumour.

目的　探讨Lambert - Eaton综合征的诊断,与原发癌肿的联系.

Conclusion The presence of oligoclonal bands and increased concentration of IgG in her spinal fluid suggests that a IgG antibodies mediated autoimmunity may play an important role in this patient's pathogenesis of acquired neuromyotonia and Lambert-Eaton myasthenic syndrome associated with lung cancer.

上述改变可能与肺癌有关，提示患者神经系统IgG介导的自身免疫异常在神经性肌强直的发病机理中起重要作用。

Objective To discuss the clinical features of Lambert-Eaton myasthenia syndrome ( LEMS) with the primary symptom of diplopia.

目的探讨以复视为首发症状的Lambert-Eaton肌无力综合征（LEMS）的临床特点。

Conclusion The diagnosis of Lambert-Eaton syndrome should rely on electromyogram and find carefully out the primary tumour.

结论Lambert－Eaton综合征确诊依靠肌电图，应进一步查找原发癌肿病变。