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mRNA COVID-19 疫苗接种后严重疾病恶化揭示疑似多发性硬化症为视神经脊髓炎谱系障碍:一例报告。

Severe disease exacerbation after mRNA COVID-19 vaccination unmasks suspected multiple sclerosis as neuromyelitis optica spectrum disorder: a case report.

机构信息

Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Albert-Schweitzer-Campus 1, 48149, Münster, Germany.

出版信息

BMC Neurol. 2022 May 18;22(1):185. doi: 10.1186/s12883-022-02698-y.

Abstract

BACKGROUND

Since the beginning of the COVID-19 pandemic and development of new vaccines, the issue of post-vaccination exacerbation or manifestation of demyelinating central nervous system (CNS) disorders has gained increasing attention.

CASE PRESENTATION

We present a case of a 68-year-old woman previously diagnosed with multiple sclerosis (MS) since the 1980s who suffered a rapidly progressive severe sensorimotor paraparesis with loss of bladder and bowel control due to an acute longitudinal extensive transverse myelitis (LETM) after immunization with the mRNA Pfizer-BioNTech COVID-19 vaccine. Detection of Aquaporin-4-antibodies (AQP4) in both serum and CSF led to diagnosis of AQP4-antibody positive neuromyelitis optica spectrum disorder (NMOSD). Treatment with intravenous corticosteroids and plasmapheresis led to a slight improvement of the patient's symptoms.

CONCLUSIONS

Pathogenic mechanisms of post-vaccination occurrence of NMOSD are still unknown. However, cases like this should make aware of rare neurological disorders manifesting after vaccination and potentially contribute to improvement of management of vaccinating patients with inflammatory CNS disorders in the future. So far two cases of AQP4-antibody positive NMOSD have been reported in association with viral vector COVID-19 vaccines. To our knowledge, we report the first case of AQP4-antibody positive NMOSD after immunization with an mRNA COVID-19-vaccine.

摘要

背景

自 COVID-19 大流行开始和新疫苗研发以来,疫苗接种后脱髓鞘中枢神经系统 (CNS) 疾病恶化或表现的问题引起了越来越多的关注。

病例介绍

我们介绍了一位 68 岁女性的病例,她在 20 世纪 80 年代被诊断患有多发性硬化症 (MS),在接种 mRNA 辉瑞-生物科技 COVID-19 疫苗后,因急性长节段横贯性脊髓炎 (LETM) 迅速进展为严重的感觉运动性截瘫,伴有膀胱和肠道功能丧失。血清和脑脊液中 Aquaporin-4 抗体 (AQP4) 的检测导致诊断为 AQP4 抗体阳性视神经脊髓炎谱系障碍 (NMOSD)。静脉注射皮质类固醇和血浆置换治疗使患者症状略有改善。

结论

疫苗接种后发生 NMOSD 的发病机制尚不清楚。然而,此类病例应引起人们对疫苗接种后罕见神经系统疾病表现的认识,并可能有助于未来改善炎症性中枢神经系统疾病患者的疫苗接种管理。迄今为止,已有两例与病毒载体 COVID-19 疫苗相关的 AQP4 抗体阳性 NMOSD 病例报告。据我们所知,我们报告了首例与 mRNA COVID-19 疫苗接种相关的 AQP4 抗体阳性 NMOSD 病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44c5/9115999/82e3ee4fc333/12883_2022_2698_Fig1_HTML.jpg

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