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导致斯特拉茨马综合征中黄斑裂孔相关性视网膜脱离的异常玻璃体视网膜界面

Abnormal Vitreoretinal Interface Leading to Macular Hole-Associated Retinal Detachment in Straatsma Syndrome.

作者信息

Bleicher Isaac D, Davila Jose, Eliott Dean

机构信息

Massachusetts Eye and Ear, Harvard Medical School, Boston, MA, USA.

出版信息

J Vitreoretin Dis. 2024 Apr 25;8(4):476-479. doi: 10.1177/24741264241250160. eCollection 2024 Jul-Aug.

Abstract

To report a case of macular hole (MH)-associated retinal detachment (RD) with Straatsma syndrome. A clinical case was retrospectively reviewed. 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. The presence of an unusually strong vitreoretinal adhesion in the area of myelinated nerve fibers and the development of a postoperative serous RD suggest that myelination may contribute to vitreoretinal adhesion and the development of MHs in Straatsma syndrome.

摘要

报告一例伴有斯特拉茨马综合征的黄斑裂孔(MH)相关视网膜脱离(RD)病例。对一例临床病例进行回顾性分析。一名患有斯特拉茨马综合征的39岁女性因MH相关RD接受治疗。通过玻璃体切除术和内界膜剥除封闭了MH,在此过程中,在有髓神经纤维区域遇到了异常强烈的玻璃体视网膜粘连。术后一天,患者出现浆液性脉络膜脱离和浆液性RD,在术后第1周时消退。患者视力最终恢复至基线水平。有髓神经纤维区域存在异常强烈的玻璃体视网膜粘连以及术后浆液性RD的发生表明,髓鞘形成可能在斯特拉茨马综合征中促成玻璃体视网膜粘连和MH的发生。

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