Autoimmune myasthenia gravis after COVID-19 in a triple vaccinated patient.

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL
Archive of clinical cases Pub Date : 2022-09-26 eCollection Date: 2022-01-01 DOI:10.22551/2022.36.0903.10212
Cristina-Georgiana Croitoru, Dan Iulian Cuciureanu, Iulian Prutianu, Petru Cianga
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引用次数: 2

Abstract

Despite a well characterized mechanism, myasthenia gravis (MG) remains a dilemma in terms of etiology. Several case reports and series of cases suggest a potential cause-effect relation between SARS-CoV-2 infection or vaccination and MG. We present the case of an autoimmune MG occurring post Covid-19 in an elderly male, vaccinated with three doses of the BNT162b2/Pfizer-BioNTech vaccine. The 78-year-old male was admitted in the Neurology Clinic in early November 2021 with double vision, bilateral ptosis, dysphonia and dysphagia, 16 days after receiving a third dose of the BNT162b2/Pfizer-BioNTech SARS-CoV-2 vaccine and 12 days after testing positive for SARS-CoV-2 infection. The symptoms began to emerge at 9 days after COVID-19 diagnosis. Clinical neurological examination included ice-pack test and intramuscular neostigmine, both with positive results. Myasthenia gravis positive diagnosis was confirmed by slow repetitive nerve stimulation and abnormally increased serum levels of antibodies against acetylcholine receptors. Due to patient's refusal of further hospitalization, he was discharged with therapy recommendations. Under treatment with oral pyridostigmine, but no oral corticosteroid due to therapeutic noncompliance, the patient was readmitted two months later with aggravated symptoms. The myasthenic crisis was successfully treated with intravenous immunoglobulins, corticosteroid therapy and oral pyridostigmine. The novelty of the current case resides in the fact that, to the best of our knowledge, appears to be the first case of MG clinically manifested after COVID-19 infection in a fully vaccinated patient.

Abstract Image

Abstract Image

三次接种后患者的自身免疫性重症肌无力
尽管有明确的机制,重症肌无力(MG)在病因方面仍然是一个困境。一些病例报告和系列病例提示SARS-CoV-2感染或疫苗接种与MG之间存在潜在的因果关系。我们报告了一名老年男性在Covid-19后发生自身免疫性MG的病例,该男性接种了三剂BNT162b2/辉瑞- biontech疫苗。这名78岁的男性在接受第三剂BNT162b2/辉瑞- biontech SARS-CoV-2疫苗16天后,在SARS-CoV-2感染检测呈阳性12天后,于2021年11月初因复视、双侧上眼睑、发音困难和吞咽困难入住神经病学诊所。新冠肺炎确诊后第9天开始出现症状。临床神经学检查包括冰袋试验和肌肉注射新斯的明,结果均为阳性。慢性反复神经刺激和血清抗乙酰胆碱受体抗体水平异常升高证实重症肌无力阳性诊断。由于病人拒绝继续住院,他在治疗建议下出院。在口服吡哆斯的明治疗下,由于治疗依从性不佳,患者未口服皮质类固醇,两个月后症状加重再次入院。通过静脉注射免疫球蛋白、皮质类固醇治疗和口服吡哆斯的明,成功地治疗了肌无力危机。目前病例的新颖性在于,据我们所知,这似乎是第一例完全接种疫苗的患者在感染COVID-19后临床表现为MG的病例。
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