Neuromyelitis optic spectrum disorder following COVID- 19 (ChAdOx1-S) vaccine

Gunarathna Rds, RM Roshiban, Jayatissa Avgam, SS Walatharaarachchi, Fernando Ahn
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Abstract

Neuromyelitis optic spectrum disorder is an autoimmune demyelinating astro- cytopathy of central nervous system. It has emerged as a distinct clinical entity following the discovery of pathogenic antibody named AQP4-IgG against aquaporin-4 water channels in astrocytes. The clinical spectrum includes optic neuritis, acute myelitis, acute brain stem syndrome, area postrema syndrome, acute diencephalic syndrome and symptomatic cerebral syndrome.This case describes a young male patient who presented with subacute onset painful visual impairment of left eye along with bilateral lower limb weakness and numbness in the background of recent vaccination for covid-19 infection. Examination revealed bilateral papillitis and bilateral flaccid paraparesis with a sensory level at T4 level. Investigations revealed a longitudinally extensive myelitis spanning the entire length of the spinal cord, bilateral optic neuritis, positive serum AQP4-IgG antibodies with negative infective screening and autoimmune profile. Central nervous system demyelination has been observed with all types of covid-19 vaccines.
接种 COVID- 19 (ChAdOx1-S) 疫苗后出现神经脊髓炎视谱系障碍
神经脊髓炎视谱系障碍是一种中枢神经系统自身免疫性脱髓鞘星形细胞病。在发现名为 AQP4-IgG 的针对星形胶质细胞中的水通道的致病抗体后,它已成为一种独特的临床实体。本病例描述的是一名年轻男性患者,由于近期接种了柯维-19 感染疫苗,出现了亚急性发作的左眼疼痛性视力障碍以及双下肢无力和麻木。检查发现他患有双侧乳头状瘤和双侧弛缓性截瘫,感觉水平位于 T4 水平。检查结果显示,脊髓炎纵向广泛,横跨脊髓全长,双侧视神经炎,血清AQP4-IgG抗体阳性,感染性筛查和自身免疫特征阴性。所有类型的covid-19疫苗均可导致中枢神经系统脱髓鞘。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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