异常玻璃体视网膜界面导致斯特拉兹马综合征黄斑孔相关性视网膜脱离

IF 0.5 Q4 OPHTHALMOLOGY
Isaac D. Bleicher, Jose Davila, D. Eliott
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引用次数: 0

摘要

导言:报告一例黄斑孔(MH)相关性视网膜脱离(RD)并伴有 Straatsma 综合征的病例。方法:回顾性分析一例临床病例:回顾性分析一例临床病例。结果一名患有 Straatsma 综合征的 39 岁女性因黄斑孔相关性视网膜脱离接受了治疗。通过玻璃体切除术和内缘膜剥离术闭合了 MH,期间在有髓神经纤维区域发现了异常牢固的玻璃体视网膜粘连。术后一天,患者出现了浆液性脉络膜渗出和浆液性 RD,这些症状在术后一周内消失。患者的视力最终恢复到基线。结论:在髓鞘化神经纤维区域出现异常强烈的玻璃体视网膜粘连以及术后出现浆液性 RD 表明,髓鞘化可能是斯特拉斯马综合征玻璃体视网膜粘连和 MHs 发病的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abnormal Vitreoretinal Interface Leading to Macular Hole–Associated Retinal Detachment in Straatsma Syndrome
Introduction: To report a case of macular hole (MH)–associated retinal detachment (RD) with Straatsma syndrome. Methods: A clinical case was retrospectively reviewed. Results: A 39-year-old woman with Straatsma syndrome was treated for an MH-associated RD. The MH was closed with vitrectomy and internal limiting membrane peeling, during which an unusually strong vitreoretinal adhesion was encountered in the area of myelinated nerve fibers. One day postoperatively, the patient developed serous choroidal effusions and a serous RD, which resolved by postoperative week 1. The patient’s vision ultimately returned to baseline. Conclusions: The presence of an unusually strong vitreoretinal adhesion in the area of myelinated nerve fibers and the development of postoperative serous RD suggest that myelination may contribute to vitreoretinal adhesion and the development of MHs in Straatsma syndrome.
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CiteScore
1.20
自引率
16.70%
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