神经免疫学

A. Ridley
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引用次数: 70

摘要

背景:已有与COVID-19相关的脱髓鞘综合征的报道,并且在较小程度上与COVID-19疫苗相关。脱髓鞘和疫苗之间的关系,一般来说,仍然存在争议。我们回顾了暴发性脱髓鞘的表现,并讨论了之前的COVID-19疫苗接种,更广泛的鉴别诊断的制定以及最终的病理诊断。病例介绍:一名80岁妇女,表现为癫痫发作、脑病、四肢瘫,最终死亡。她在前一天接种了SARS-CoV-2疫苗。影像学显示增强的大脑病变,纵向广泛的横贯脊髓炎。脑脊液明显炎症。病理检查的中枢神经系统病变显示脱髓鞘和炎症超越白质,不局限于静脉周围分布。结论:本病例表现为弥漫性脱髓鞘综合征的暴发性病程,临床病理特征为马尔堡变异型多发性硬化症。该病例有几个独特的方面,包括病程极快,脑脊液异常的异常演变,伴低糖血症和明显升高的蛋白。虽然我们不能明确地证明因果关系,但接近接种疫苗是一种相关的联系
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Neuroimmunology
Background: There have been reports of demyelinating syndromes in association with COVID-19 and to a much lesser extent COVID 19 vaccines. The association between demyelination and vaccines, in general, remains controversial. We review a presentation of fulminant demyelination, and discuss antecedent COVID-19 vaccination, the formulation of a broader differential diagnosis and ultimately the pathologic diagnosis. Case presentation: An 80-year-old woman presented with seizure, encephalopathy, quadriparesis and ultimately expired. She received a SARS-CoV-2 vaccine one day prior. Imaging revealed contrast enhancing cerebral lesions, longitudinally extensive transverse myelitis. CSF was markedly inflammatory. Pathologic examination of the CNS lesions revealed demyelination and inflammation beyond white matter, not restricted to a perivenular distribution. Conclusion: This case depicts a seemingly fulminant course of a diffuse demyelinating syndrome characterized clinicopathologically as Marburg’s variant of multiple sclerosis. There are several unique aspects of this case including the extremely rapid course, the unusual evolution of CSF abnormalities, with hypoglycorrhachia and markedly elevated protein. The proximity to vaccination is a pertinent association to document, though we cannot unequivocally prove causation
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