Suppr超能文献

[伴或不伴支气管源性癌的伊顿 - 兰伯特型肌无力综合征患者神经肌肉传递状态与诱发皮肤交感神经电位的比较评估]

[Comparative evaluation of the status of neuromuscular transmission and evoked skin sympathetic potential in myasthenia syndrome of the Eaton-Lambert type in patients with and without bronchogenic carcinoma].

作者信息

Bzhilianskiĭ M A, Sanadze A G

出版信息

Zh Nevropatol Psikhiatr Im S S Korsakova. 1990;90(9):21-5.

PMID:2176034
Abstract

Neuromuscular transmission and evoked skin sympathetic potential (ESSP) were examined in 14 patients with Lambert-Eaton syndrome. Bronchogenous lung carcinoma was revealed in four of those patients. No correlation was found between the impairment of neuromuscular transmission and the parameters of ESSP. All the four patients suffering from Lambert-Eaton syndrome combined with bronchogenous lung carcinoma did not manifest ESSP. The reversibility of ESSP disorders established after amiridine and guanidine administration attest to the mediatory character of vegetative regulation impairment in patients with the myasthenic syndrome under discussion.

摘要

对14例兰伯特-伊顿综合征患者进行了神经肌肉传递和诱发性皮肤交感神经电位(ESSP)检查。其中4例患者发现有支气管源性肺癌。未发现神经肌肉传递损害与ESSP参数之间存在相关性。所有4例合并支气管源性肺癌的兰伯特-伊顿综合征患者均未表现出ESSP。给予阿米三嗪和胍后ESSP障碍的可逆性证明了所讨论的肌无力综合征患者自主调节损害的中介性质。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验