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引用次数: 23

摘要

重症肌无力是一种常见的自身免疫性疾病,其特征是存在针对乙酰胆碱受体的致病性抗体。患者表现为不同程度和分布的波动性虚弱,有时危及生命。临床表现,建立诊断,重症肌无力的自然史,和治疗方案在此进行综述。兰伯特-伊顿综合征(肌无力综合征)则不常见,这是另一种自身免疫性疾病,由于存在针对pq型电压门控钙通道的抗体。总结临床特点及治疗方案。
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Myasthenia gravis and Lambert-Eaton syndrome.
Myasthenia gravis is a common autoimmune disorder characterized by the presence of pathogenic antibodies directed against the acetylcholine receptor. Patients present with variable degrees and distribution of fluctuating weakness at times life threatening. Clinical manifestations, establishment of diagnosis, the natural history of myasthenia gravis, and therapeutic options are herein reviewed. Far less common is Lambert-Eaton syndrome (the myasthenic syndrome), another autoimmune disorder due to the presence of antibodies directed against the PQ-type voltage-gated calcium channels. Clinical features and treatment options are summarized.
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