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髓鞘少突胶质细胞糖蛋白抗体相关性双侧视神经炎伴单侧玻璃体内前部出血。

Myelin oligodendrocyte glycoprotein antibody-associated bilateral optic neuritis with unilateral prepapillary vitreous hemorrhage.

机构信息

Department of Ophthalmology, Fremantle Hospital, Perth WA Australia.

Department of Medical Imaging, Perth Children's Hospital WA Australia.

出版信息

J AAPOS. 2022 Jun;26(3):161-164. doi: 10.1016/j.jaapos.2022.02.007. Epub 2022 May 4.

Abstract

We present a case of bilateral myelin oligodendrocyte glycoprotein antibody optic neuritis (MOG-ON) with unilateral vitreous hemorrhage in a 6-year-old boy. Multidisciplinary team care, including extensive investigations and prolonged follow-up, excluded alternative causes of vitreous hemorrhage. Early suspicion and diagnosis of MOG-ON led to timely intravenous methylprednisolone treatment, with protracted oral steroid taper, resulting in complete resolution of optic nerve swelling, vitreous hemorrhage, and visual function.

摘要

我们报告了一例 6 岁男孩双侧髓鞘少突胶质细胞糖蛋白抗体视神经炎(MOG-ON)合并单侧玻璃体积血。多学科团队的治疗,包括广泛的检查和长期随访,排除了玻璃体积血的其他原因。早期怀疑和诊断 MOG-ON 导致及时静脉注射甲基强的松龙治疗,并进行长期口服类固醇减量,最终完全缓解视神经肿胀、玻璃体积血和视力功能。

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