Suppr超能文献

重症肌无力患者合并抗髓鞘少突胶质细胞糖蛋白及抗水通道蛋白4抗体阳性的视神经脊髓炎谱系疾病

Anti-MOG and Anti-AQP4 positive neuromyelitis optica spectrum disorder in a patient with myasthenia gravis.

作者信息

Bates Molly, Chisholm Jason, Miller Eric, Avasarala Jagannadha, Guduru Zain

机构信息

University of Kentucky, Department of Neurology, USA.

出版信息

Mult Scler Relat Disord. 2020 Sep;44:102205. doi: 10.1016/j.msard.2020.102205. Epub 2020 May 23.

Abstract

Aquaporin 4 antibody (anti-AQP4) positive neuromyelitis optica spectrum disorder (NMOSD) is known to occur in the setting of myasthenia gravis (MG). However, comorbid MG with myelin oligodendrocyte glycoprotein antibody (anti-MOG) positive NMOSD has not been reported. We present a case of anti-MOG and anti-AQP4 positive NMOSD in a patient with long-standing MG. The patient presented with acute right-sided weakness with MRI demonstrating extensive spinal cord edema extending from T2 to the medulla with associated contrast enhancement. To our knowledge, this is the first reported case of anti-MOG and anti-AQP4 positive NMOSD in a patient with known MG.

摘要

水通道蛋白4抗体(抗AQP4)阳性的视神经脊髓炎谱系障碍(NMOSD)已知可发生于重症肌无力(MG)患者中。然而,合并重症肌无力的髓鞘少突胶质细胞糖蛋白抗体(抗MOG)阳性的NMOSD尚未见报道。我们报告1例长期患有重症肌无力的抗MOG和抗AQP4阳性的NMOSD患者。该患者表现为急性右侧肢体无力,MRI显示广泛的脊髓水肿,从T2延伸至延髓,并伴有对比增强。据我们所知,这是首例已知患有重症肌无力的抗MOG和抗AQP4阳性的NMOSD病例。

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