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牵牛花综合征合并牵拉性孔源性视网膜脱离的治疗

Treatment of combined traction-rhegmatogenous retinal detachment in the morning glory syndrome.

作者信息

Harris M J, de Bustros S, Michels R G, Joondeph H C

出版信息

Retina. 1984 Fall-Winter;4(4):249-52. doi: 10.1097/00006982-198400440-00007.

DOI:10.1097/00006982-198400440-00007
PMID:6543402
Abstract

A 14-year-old boy had a near total retinal detachment associated with the morning glory optic disc anomaly. A tiny slit-like retinal break with adjacent vitreous traction was found within the coloboma, providing communication between the vitreous cavity and the subretinal space. Vitrectomy, fluid-gas exchange, and postoperative confluent Krypton laser photocoagulation around the optic disc resulted in a successful reattachment of the retina. The retina has remained attached for 14 months.

摘要

一名14岁男孩发生了与牵牛花视盘异常相关的近乎完全性视网膜脱离。在缺损区内发现一个微小的裂隙样视网膜裂孔及相邻的玻璃体牵拉,使得玻璃体腔与视网膜下间隙相通。玻璃体切除术、液-气交换以及术后对视盘周围进行氪激光光凝融合术,使视网膜成功复位。视网膜已保持复位14个月。

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Treatment of combined traction-rhegmatogenous retinal detachment in the morning glory syndrome.牵牛花综合征合并牵拉性孔源性视网膜脱离的治疗
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Front Med (Lausanne). 2022 May 16;9:826860. doi: 10.3389/fmed.2022.826860. eCollection 2022.
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Int J Ophthalmol. 2022 May 18;15(5):766-772. doi: 10.18240/ijo.2022.05.12. eCollection 2022.
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Recurrent proliferative vitreoretinopathy in a patient with morning glory syndrome and intellectual disability.一名患有牵牛花综合征和智力障碍的患者发生复发性增殖性玻璃体视网膜病变。
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Postoperative follow-up of a case of atypical morning glory syndrome associated with persistent fetal vasculature.一例与持续性胎儿血管系统相关的非典型牵牛花综合征病例的术后随访。
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Intraoperative optical coherence tomography assisted analysis of pars Plana vitrectomy for retinal detachment in morning glory syndrome: a case report.术中光学相干断层扫描辅助分析牵牛花综合征视网膜脱离的玻璃体切除术:病例报告
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