[A case of myasthenia gravis with coexistence of anti-acetylcholine receptor antibodies and anti-P/Q-type VGCC antibodies].

Q4 Medicine
Clinical Neurology Pub Date : 2024-04-24 Epub Date: 2024-03-20 DOI:10.5692/clinicalneurol.cn-001945
Yuki Takeda, Yoshikatsu Noda, Naohiko Seike, Hiroyuki Ishihara
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引用次数: 0

Abstract

A 79-year-old woman who presented ptosis and dysphagia were admitted to our hospital. Anti-acetylcholine receptor antibodies and anti-P/Q-type VGCC antibodies were both positive. Electrophysiological examination showed postsynaptic pattern which supported myasthenia gravis. She did not meet the diagnostic criteria for Lambert-Eaton myasthenic syndrome (LEMS). In cases which these antibodies coexist, careful electrophysiological evaluation is required for the diagnosis. In addition, although anti-P/Q-type VGCC antibodies have been specific to LEMS, patients with these antibodies represent various symptoms other than LEMS. Low and middle titer of the antibodies may be not specific to LEMS.

[一例同时存在抗乙酰胆碱受体抗体和抗 P/Q 型 VGCC 抗体的重症肌无力病例]。
本院收治了一名出现上睑下垂和吞咽困难的 79 岁女性。抗乙酰胆碱受体抗体和抗P/Q型VGCC抗体均呈阳性。电生理检查显示突触后模式支持重症肌无力。她不符合兰伯特-伊顿肌萎缩综合征(LEMS)的诊断标准。在这些抗体同时存在的情况下,需要进行仔细的电生理评估才能确诊。此外,虽然抗 P/Q 型 VGCC 抗体是 LEMS 的特异性抗体,但有这些抗体的患者会表现出 LEMS 以外的各种症状。低滴度和中等滴度的抗体可能对 LEMS 没有特异性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical Neurology
Clinical Neurology Medicine-Neurology (clinical)
CiteScore
0.30
自引率
0.00%
发文量
147
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