Suppr超能文献

髓鞘少突胶质细胞糖蛋白抗体相关疾病(MOGAD)中的广泛脑干病变:一例报告

Extensive brainstem lesions in myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD): A case report.

作者信息

Kojita Yasuyuki, Okada Nonoka, Hirakawa Mayumi, Fujii Kanako, Satou Takao, Ishii Kazunari

机构信息

Department of Radiology, Kindai University Faculty of Medicine, Osaka, Japan.

出版信息

Radiol Case Rep. 2024 Sep 6;19(12):5589-5594. doi: 10.1016/j.radcr.2024.08.032. eCollection 2024 Dec.

Abstract

Myelin oligodendrocyte glycoprotein antibody-associated disease is a group of central nervous system demyelinating disorders caused by autoantibodies. While myelin oligodendrocyte glycoprotein antibody-associated disease typically presents as optic neuritis and myelitis in adults, this case report details a patient with brainstem lesions. A 45-year-old male presented with episodes of vertigo, nystagmus, and diplopia in left lateral gaze, which had persisted for 2 months, accompanied by headache. Computed tomography showed hyperdensity extending from the left side of the pons to the middle cerebellar peduncle. Magnetic resonance imaging revealed lesions exhibiting heterogeneous diffusion restriction, with enhancement that included granular and linear patterns. F-fluorodeoxyglucose positron emission tomography demonstrated increased uptake in these lesions. Following further evaluation, myelin oligodendrocyte glycoprotein antibody-associated disease was diagnosed. Treatment with high-dose corticosteroids initially alleviated symptoms, but symptoms flared upon reduction of the steroids. This case underscores the importance of considering myelin oligodendrocyte glycoprotein antibody-associated disease in the differential diagnosis of brainstem lesions and discusses distinguishing imaging features from similar conditions.

摘要

髓鞘少突胶质细胞糖蛋白抗体相关疾病是一组由自身抗体引起的中枢神经系统脱髓鞘疾病。虽然髓鞘少突胶质细胞糖蛋白抗体相关疾病在成人中通常表现为视神经炎和脊髓炎,但本病例报告详细介绍了一名患有脑干病变的患者。一名45岁男性出现眩晕、眼球震颤以及左侧凝视时复视发作,持续2个月,并伴有头痛。计算机断层扫描显示高密度影从脑桥左侧延伸至小脑中脚。磁共振成像显示病变呈现异质性扩散受限,强化包括颗粒状和线状模式。F-氟脱氧葡萄糖正电子发射断层扫描显示这些病变摄取增加。经过进一步评估,诊断为髓鞘少突胶质细胞糖蛋白抗体相关疾病。高剂量皮质类固醇治疗最初缓解了症状,但在减少类固醇剂量后症状复发。本病例强调了在脑干病变的鉴别诊断中考虑髓鞘少突胶质细胞糖蛋白抗体相关疾病的重要性,并讨论了与类似疾病相区别的影像学特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da99/11406359/480392f20168/gr1.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