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两名多发性硬化症患者先前患有抗N-甲基-D-天冬氨酸受体脑炎。

Antecedent anti-NMDA receptor encephalitis in two patients with multiple sclerosis.

作者信息

Baheerathan A, Brownlee W J, Chard D T, Shields K, Gregory R, Trip S A

机构信息

National Hospital for Neurology and Neurosurgery, London, United Kingdom.

Queen Square Multiple Sclerosis Centre, UCL Institute of Neurology, London, United Kingdom.

出版信息

Mult Scler Relat Disord. 2017 Feb;12:20-22. doi: 10.1016/j.msard.2016.12.009. Epub 2016 Dec 29.

Abstract

Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is an autoimmune disorder characterised by psychiatric symptoms, movement disorder and seizures often evolving into a severe encephalopathy. An overlap has recently been recognised between anti-NMDAR encephalitis and inflammatory demyelinating disorders, particularly neuromyelitis optical spectrum disorder (NMOSD). In this case report, we describe two patients with an initial presentation consistent with anti-NMDAR encephalitis who have subsequently developed relapsing-remitting multiple sclerosis (MS) and discuss the literature pertaining to potential overlap between NMDAR encephalitis and inflammatory demyelinating disorders.

摘要

抗N-甲基-D-天冬氨酸受体(NMDAR)脑炎是一种自身免疫性疾病,其特征为精神症状、运动障碍和癫痫发作,常发展为严重脑病。最近人们认识到抗NMDAR脑炎与炎性脱髓鞘疾病,特别是视神经脊髓炎谱系障碍(NMOSD)之间存在重叠。在本病例报告中,我们描述了两名最初表现符合抗NMDAR脑炎的患者,他们随后发展为复发缓解型多发性硬化症(MS),并讨论了有关NMDAR脑炎与炎性脱髓鞘疾病之间潜在重叠的文献。

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