New Onset of Myasthenia Gravis following COVID-19 Vaccination: A Case Report

Fatemeh Afrashteh
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Abstract

Myasthenia gravis (MG) is a rare autoimmune disease and the most common neuromuscular junction disorder. The most common symptoms are diplopia, ptosis, and fluctuating weakness of ocular and limb muscles. Here we report a case of MG after COVID-19 vaccination. A 37-year-old Iranian lady presented with generalized weakness, diplopia, and ptosis after three days from taking the second dose of COVID-19 vaccine. Symptoms began three days after taking the second dose of Sinopharm BIBP COVID-19 vaccine (BBIBP-CorV) and worsened within a week. Her past medical history included migraine-type headaches and gastric reflux. She was consuming Rizatriptan and Nortriptyline for her migraine headache and Pantoprazole, Domperidone, and Sertraline for stomach reflux. She had a family history of Essential tremor in her father, uncle, and grandfather. Antibody against the acetylcholine receptor (AChR-Ab) was more than eight times compared to the normal range. The pattern of repetitive nerve stimulation was suggestive for MG. Treatment with corticosteroid, azathioprine, and pyridostigmin led to amelioration of symptoms. Follow-up testing revealed AChR-Ab returned to the normal range. There are some case reports in that a chronic autoimmune disorder flared up after the COVID1-9 infection or its vaccination. There are several reports of MG exacerbations, acute respiratory distress syndrome, higher ICU admission, and mortality rate and worsening neurological symptoms after COVID-19 infection. There is still debate about the association between neuromuscular disorders and COVID-19 infection and vaccination. This matter is more doubtful for myasthenia gravis.
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COVID-19疫苗接种后新发重症肌无力1例报告
重症肌无力是一种罕见的自身免疫性疾病,也是最常见的神经肌肉连接障碍。最常见的症状是复视、上睑下垂、眼部和四肢肌肉的波动性无力。我们在此报告一例COVID-19疫苗接种后的MG病例。一名37岁的伊朗妇女在接种第二剂COVID-19疫苗三天后出现全身无力、复视和上睑下垂。在接种第二剂国药BIBP- corv后3天开始出现症状,并在一周内恶化。既往病史包括偏头痛型头痛和胃反流。她服用利扎曲坦和去甲替林治疗偏头痛,泮托拉唑、多潘立酮和舍曲林治疗胃反流。她的父亲、叔叔和祖父都有特发性震颤的家族史。抗乙酰胆碱受体(AChR-Ab)抗体是正常范围的8倍以上。重复神经刺激模式提示MG。用皮质类固醇、硫唑嘌呤和吡虫胺治疗可改善症状。后续检测显示AChR-Ab恢复到正常范围。有报道称,在感染新冠病毒或接种新冠病毒疫苗后,出现了慢性自身免疫性疾病。有几篇报道称,COVID-19感染后MG加重、急性呼吸窘迫综合征、ICU住院率升高、死亡率升高、神经系统症状恶化。神经肌肉疾病与COVID-19感染和疫苗接种之间的关系仍存在争议。重症肌无力患者更值得怀疑。
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