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一例抗水通道蛋白4抗体阳性的视神经脊髓炎谱系障碍,腰椎神经根存在MRI证实的病变。

A case of anti-AQP4 antibody-positive neuromyelitis optica spectrum disorder with MRI-proven lesions in lumbar nerve roots.

作者信息

Toru Shuta, Soejima Itsuki, Katayama Yuki, Saito Kazuyuki, Yokote Hiroaki

机构信息

Department of Neurology, Nitobe Memorial Nakano General Hospital, 4-59-16 Chuo, Nakano-ku, Tokyo 164-8607, Japan.

Department of Neurology, Nitobe Memorial Nakano General Hospital, 4-59-16 Chuo, Nakano-ku, Tokyo 164-8607, Japan.

出版信息

Mult Scler Relat Disord. 2020 Nov;46:102557. doi: 10.1016/j.msard.2020.102557. Epub 2020 Oct 2.

Abstract

Neuromyelitis optica spectrum disorder (NMOSD) affects the central nervous system but is rarely reported to cause peripheral nervous system damage. We report a case of a 57-year-old woman with numbness and muscle weakness of the left lower limb during the course of 12 years of anti-AQP4 antibody-positive NMOSD. Lumbar magnetic resonance imaging (MRI) showed a contrast effect on the left L4, L5, and S1 nerve roots, which is a highly unusual presentation. Although radiculopathy without myelopathy is unusual in AQP4-positive NMOSD, the MRI-confirmed nerve root lesions in our case indicate that it can occur.

摘要

视神经脊髓炎谱系障碍(NMOSD)累及中枢神经系统,但很少有导致周围神经系统损害的报道。我们报告一例57岁女性,在抗水通道蛋白4(AQP4)抗体阳性的NMOSD病程12年中出现左下肢麻木和肌无力。腰椎磁共振成像(MRI)显示左侧L4、L5和S1神经根有强化效应,这是一种非常罕见的表现。虽然在AQP4阳性的NMOSD中无脊髓病的神经根病并不常见,但我们病例中MRI证实的神经根病变表明这种情况是可能发生的。

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