Spontaneously resolving late-onset ocular myasthenia related to COVID-19. A case report.

Cyprian Popescu
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Abstract

Myasthenia gravis (MG) is the most common disease of the neuromuscular junction disorders with bimodal distribution of age, which is often under-estimated in the elderly. Some clinical cases show an association between MG and COVID-19, since molecular mimicry between SARS-CoV-2 and AChR proteins could be responsible for the onset of the disease. We report a 77-year-old woman who developed right eyelid ptosis five days after COVID-19 infection. Positive serum anti-acetylcholine receptor antibodies allowed the diagnosis of myasthenia gravis. It should be noted that there were no significant decremental changes on 3 Hz repetitive motor nerve stimulation study, even for the affected orbicularis oculi muscle. Clinical and pathophysiological data suggest that inflammation during COVID-19 could trigger an overproduction of autoantibodies previously present in the body at a subclinical level. This is the first case of COVID-19 infection complicated by myasthenia gravis, to the best of our knowledge, that resolves spontaneously.

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与 COVID-19 有关的自发缓解的晚发性眼肌症。病例报告。
重症肌无力(MG)是神经肌肉接头疾病中最常见的疾病,其发病年龄呈双峰分布,老年人的发病率往往被低估。一些临床病例显示,MG与COVID-19有关联,因为SARS-CoV-2和AChR蛋白之间的分子模拟可能是该病发病的原因。我们报告了一名 77 岁的妇女,她在感染 COVID-19 五天后出现右眼睑下垂。血清中抗乙酰胆碱受体抗体阳性,诊断为重症肌无力。值得注意的是,在 3 赫兹重复性运动神经刺激研究中,即使是受影响的眼轮匝肌也没有明显的功能减退变化。临床和病理生理学数据表明,COVID-19 期间的炎症可能引发体内亚临床水平的自身抗体过度产生。据我们所知,这是第一例感染 COVID-19 并发重症肌无力并能自愈的病例。
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