A Case of Myasthenia Gravis Diagnosed After Hospitalization in a Patient Receiving Home Oxygen Therapy for Respiratory Failure.

IF 1.4 Q2 MEDICINE, GENERAL & INTERNAL
Acute Medicine & Surgery Pub Date : 2026-04-26 eCollection Date: 2026-01-01 DOI:10.1002/ams2.70127
Yuki Yamamoto, Atsunori Onoe, Shohei Ono, Yoshihiro Nakamura, Takahiro Oishi, Fumiko Nakamura, Mari Nakajima, Kazuhito Sakuramoto, Takashi Muroya, Kentaro Kajino, Hitoshi Ikegawa, Yasuyuki Kuwagata
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引用次数: 0

Abstract

Introduction: Respiratory failure has various causes, including neuromuscular disorders. We report a case of myasthenic crisis requiring intensive care after a delayed diagnosis.

Case presentation: A woman in her 70s had been on home oxygen therapy for 10 months due to dyspnea. She was admitted with worsening dyspnea, type II respiratory failure, and pneumonia requiring mechanical ventilation. Although her pneumonia improved, ventilator weaning was unsuccessful. Muscle weakness raised suspicion of neuromuscular disease. Myasthenia gravis was a differential diagnosis, but she showed no thymoma, ocular symptoms, or abnormal findings on edrophonium or repetitive nerve stimulation tests. On Day 19, she tested positive for MuSK antibodies and myasthenia gravis was diagnosed. She was treated with prednisone, tacrolimus, intravenous immunoglobulin, and plasmapheresis. She was successfully weaned from mechanical ventilation and discharged home on hospital Day 81.

Conclusion: Myasthenia gravis should be considered as a differential diagnosis of unexplained respiratory failure.

因呼吸衰竭住院接受家庭吸氧治疗的重症肌无力1例。
呼吸衰竭有多种原因,包括神经肌肉疾病。我们报告一例肌无力危机需要重症监护后延迟诊断。病例介绍:一位70多岁的妇女因呼吸困难在家吸氧10个月。她入院时呼吸困难加重,II型呼吸衰竭,肺炎需要机械通气。虽然她的肺炎有所好转,但仍未成功脱下呼吸机。肌肉无力引起对神经肌肉疾病的怀疑。重症肌无力是一种鉴别诊断,但她没有胸腺瘤、眼部症状,也没有脑电波或重复神经刺激试验的异常发现。第19天,她的MuSK抗体检测呈阳性,被诊断为重症肌无力。她接受强的松、他克莫司、静脉注射免疫球蛋白和血浆置换治疗。她成功脱离机械通气,并于第81天出院回家。结论:重症肌无力应作为不明原因呼吸衰竭的鉴别诊断。
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
Acute Medicine & Surgery
Acute Medicine & Surgery MEDICINE, GENERAL & INTERNAL-
自引率
12.50%
发文量
87
审稿时长
53 weeks
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