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重症监护病房获得性肌无力的神经生理学与肌肉组织病理学:从 COVID-19 中吸取的教训

Neurophysiology and muscle histopathology in ICU-acquired muscle weakness: Lessons learned from COVID-19.

作者信息

Hejbøl Eva K, Lomstein Atle V, Schrøder Henrik D, Khan Benjamin, Harbo Thomas, Tankisi Hatice

机构信息

Department of Pathology, Odense University Hospital, Odense, Denmark.

Department of Neurology, Aarhus University Hospital, Aarhus, Denmark.

出版信息

Clin Neurophysiol Pract. 2025 May 7;10:172-180. doi: 10.1016/j.cnp.2025.05.001. eCollection 2025.

DOI:10.1016/j.cnp.2025.05.001
PMID:40486243
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12145520/
Abstract

OBJECTIVE

To describe different electrophysiological, histopathological, and ultrastructural patterns of muscle pathology in COVID-19-associated intensive care unit acquired weakness (ICUAW) and raise the question of whether COVID-19-associated critical illness myopathy (CIM) is a distinct entity or is similar to CIM of other causes.

METHODS

A series of three patients with COVID-19-associated ICUAW were presented.Clinical examination, electrophysiological testing, and muscle pathology with light and electron microscopy were reported systematically.

RESULTS

All three patients were clinically affected with severe proximal and distal weakness of upper and lower extremities, increased plasma levels of muscle enzymes, and had myopathic electromyography. Furthermore, in two patients, electrophysiological signs of inflammatory myopathy with profuse denervation activity were present. Muscle pathologies were prominent but very diverse. One patient had signs of CIM, another showed severe inflammatory myopathy, and the main finding in the third patient was mitochondrial changes.

CONCLUSION

Although the three cases showed similar clinical and electrophysiological patterns, muscle pathology revealed distinct underlying features. This spectrum of muscle disease among patients with severe COVID-19 includes CIM, autoimmune response to the COVID-19 infection, and mitochondrial dysfunction.

SIGNIFICANCE

Electrophysiology and histopathology complement each other and are important for determining the etiology, as well as guiding treatment and prognosis.

摘要

目的

描述新型冠状病毒肺炎(COVID-19)相关重症监护病房获得性肌无力(ICUAW)中不同的肌肉病理学电生理、组织病理学和超微结构模式,并提出COVID-19相关危重病性肌病(CIM)是一种独特的疾病实体还是与其他病因导致的CIM相似的问题。

方法

报告了3例COVID-19相关ICUAW患者。系统介绍了临床检查、电生理测试以及光镜和电镜下的肌肉病理学检查结果。

结果

所有3例患者临床上均出现严重的四肢近端和远端肌无力、肌肉酶血浆水平升高以及肌病性肌电图表现。此外,2例患者存在伴有大量失神经活动的炎性肌病的电生理征象。肌肉病理学表现突出但差异很大。1例患者有CIM体征,另1例表现为严重的炎性肌病,第3例患者的主要发现是线粒体改变。

结论

尽管3例患者表现出相似的临床和电生理模式,但肌肉病理学显示出不同的潜在特征。重症COVID-19患者中的这种肌肉疾病谱包括CIM、对COVID-19感染的自身免疫反应以及线粒体功能障碍。

意义

电生理学和组织病理学相互补充,对于确定病因以及指导治疗和判断预后很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fa8/12145520/b3448cc508bc/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fa8/12145520/435075b7e1db/gr1a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fa8/12145520/0e180c07079e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fa8/12145520/0cb4df0a6c2d/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fa8/12145520/b3448cc508bc/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fa8/12145520/435075b7e1db/gr1a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fa8/12145520/0e180c07079e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fa8/12145520/0cb4df0a6c2d/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fa8/12145520/b3448cc508bc/gr4.jpg

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Compound Muscle Action Potential and Myosin-Loss Pathology in Patients With Critical Illness Myopathy: Correlation and Prognostication.
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Neurology. 2024 Jul 9;103(1):e209496. doi: 10.1212/WNL.0000000000209496. Epub 2024 Jun 13.
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Beyond the acute: pain in long COVID survivors at 1.5 years.超越急性期:长新冠幸存者 1.5 年后的疼痛。
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