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重症肌无力危象合并黏液性水肿,抗乙酰胆碱受体抗体和抗肌肉特异性酪氨酸激酶抗体均为阳性。

Myasthenic Crisis Complicated with Myxedema, Positive for Both Anti-acetylcholine Receptor and Anti-muscle-specific Tyrosine Kinase Antibodies.

作者信息

Horiuchi Kazuhiro, Nagai Azusa, Wakita Masahiro, Ito Shotaro, Takamura Kei, Houzen Hideki

机构信息

Department of Neurology, Obihiro Kosei General Hospital, Japan.

First Department of Medicine, Obihiro Kosei General Hospital, Japan.

出版信息

Intern Med. 2018 Jan 15;57(2):265-268. doi: 10.2169/internalmedicine.9291-17. Epub 2017 Nov 1.

Abstract

We herein report the case of myasthenic crisis occurring in a 51-year-old man. He had experienced ptosis, increased body weight with edema, and fatigue with dyspnea. He presented at our emergency department with disturbed consciousness. He was originally diagnosed with myxedema coma, and he required artificial respiration. Because his weakness persisted and he was positive for anti-acetylcholine receptor antibodies and anti-muscle-specific tyrosine kinase antibodies, we diagnosed myasthenic crisis after various examinations. His clinical response to treatment was good and he was discharged in an ambulatory status 3 months after admission. This case demonstrates that myasthenic crisis may occur in association with myxedema.

摘要

我们在此报告一例发生在一名51岁男性身上的重症肌无力危象。他曾经历上睑下垂、体重增加伴水肿以及疲劳和呼吸困难。他因意识障碍被送至我们的急诊科。他最初被诊断为黏液性水肿昏迷,需要人工呼吸。由于他的肌无力持续存在,且抗乙酰胆碱受体抗体和抗肌肉特异性酪氨酸激酶抗体呈阳性,经过各种检查后我们诊断为重症肌无力危象。他对治疗的临床反应良好,入院3个月后以非卧床状态出院。该病例表明重症肌无力危象可能与黏液性水肿相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/601c/5820048/09d4652a2373/1349-7235-57-0265-g001.jpg

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