Suppr超能文献

动眼神经和面神经同时麻痹:抗水通道蛋白4抗体阳性视神经脊髓炎的一种罕见表现。

Concomitant abducens and facial nerve palsies: A rare presentation in anti-aquaporin-4 antibody-positive neuromyelitis optica.

作者信息

Oo Kok-Tian, Tay Kim-Siang, Law Wan-Chung, Shatriah Ismail

机构信息

Department of Ophthalmology, School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.

Department of Neuromedicine, Hospital Umum Sarawak, Jalan Hospital, Kuching, Sarawak, Malaysia.

出版信息

Taiwan J Ophthalmol. 2019 Dec 5;10(3):235-238. doi: 10.4103/tjo.tjo_69_19. eCollection 2020 Jul-Sep.

Abstract

Over the past decade, the discovery of disease-specific aquaporin-4 antibodies has led to a better understanding of the diverse spectrum of disorders that are associated with neuromyelitis optica. Brainstem manifestations have been increasingly recognized in this disease. However, multiple cranial nerve palsies as an initial presentation of neuromyelitis optica are uncommon. We report a rare case of anti-aquaporin-4 antibody-positive neuromyelitis optica that presented with unilateral abducens and facial nerve palsies. Notably, this case did not involve the optic nerve or the spinal cord. Diagnosing neuromyelitis optica that presents as an isolated acute brainstem syndrome is challenging, but the outcome may be devastating if the diagnosis is delayed.

摘要

在过去十年中,疾病特异性水通道蛋白4抗体的发现使人们对与视神经脊髓炎相关的各种疾病有了更好的理解。脑干表现在此疾病中越来越受到认可。然而,以多发性颅神经麻痹作为视神经脊髓炎的初始表现并不常见。我们报告了一例罕见的抗水通道蛋白4抗体阳性的视神经脊髓炎,其表现为单侧展神经和面神经麻痹。值得注意的是,该病例未累及视神经或脊髓。诊断表现为孤立性急性脑干综合征的视神经脊髓炎具有挑战性,但如果诊断延迟,后果可能是毁灭性的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a88/7585481/5b1637e01c1e/TJO-10-235-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验