Department of Ophthalmology, APC 7, Rhode Island Hospital, 593 Eddy Street, Providence, RI 02903, USA.
J Neuroophthalmol. 2010 Jun;30(2):123-5. doi: 10.1097/WNO.0b013e3181ce199e.
A 31-year-old woman with morning glory optic disc anomaly (MGDA) developed acute retrobulbar optic neuritis and a bullous macular detachment. MRI demonstrated truncation of the perineural space of the affected optic nerve as well as focal optic nerve enhancement. Optical coherence tomography (OCT) showed retinoschisis associated with the macular detachment. The MRI and OCT findings support the vitreous as the source of the subretinal fluid. This is the first reported case of optic neuritis in MGDA.
一位 31 岁女性患有牵牛花综合征（MGDA），出现急性球后视神经炎和大疱性黄斑脱离。MRI 显示受累视神经的神经周围间隙截断，以及视神经局灶性增强。光学相干断层扫描（OCT）显示黄斑脱离伴视网膜劈裂。MRI 和 OCT 结果支持玻璃体内是视网膜下液的来源。这是首例 MGDA 合并视神经炎的报告病例。
