Matsumoto H, Sugiyama T, Ito M, Yachi A
J Neurol Sci. 1982 Nov-Dec;57(1):83-8. doi: 10.1016/0022-510x(82)90112-5.
Myasthenia gravis developed acutely in a 32-year-old woman, who incidentally was found to have myotonia congenita of the autosomal dominant mode of inheritance. The simultaneous occurrence of myasthenia gravis and myotonia congenita was established clinically, pharmacologically and electromyographically. There was no immunologic abnormality, whereas the thymus was detected by pneumomediastinographic tomograms. About 2 months after the onset of myasthenia gravis, thymectomy was performed resulting in progressive improvement of myasthenia without apparent change in the myotonia.
一名32岁女性急性发生重症肌无力,偶然发现其患有常染色体显性遗传模式的先天性肌强直。重症肌无力和先天性肌强直的同时出现通过临床、药理学和肌电图检查得以确诊。不存在免疫异常,而通过纵隔充气造影断层扫描检测到胸腺。重症肌无力发病约2个月后进行了胸腺切除术,结果重症肌无力逐渐改善,而肌强直无明显变化。