Lobzin V S, Kosachev V D, Sidorova T G, Rudenko D I
Zh Nevropatol Psikhiatr Im S S Korsakova. 1990;90(9):91-4.
Six patients with Lambert-Eaton myasthenic syndrome were analyzed for the character of the initial symptoms, the clinical course and typical lesions on electrophysiological and x-ray studies. The given myasthenic syndrome often anticipates tumor symptoms and patients, as a rule, are seen for a long time by neuropathologists with a diagnosis of myasthenia. The data of ours indicate a real opportunity of the use of neurological and electromyographic criteria for goal-oriented search of bronchogenic carcinoma at the earlier stages of its development.
对6例兰伯特-伊顿肌无力综合征患者的初始症状特征、临床病程以及电生理和X线研究中的典型病变进行了分析。所提及的肌无力综合征常常先于肿瘤症状出现，并且通常神经病理学家会在很长一段时间内将患者诊断为肌无力。我们的数据表明，在支气管源性癌发展的早期阶段，利用神经学和肌电图标准进行有针对性的搜索具有切实的可能性。
