Early recurrence of macular schisis in X-linked retinoschisis treated with vitrectomy for rhegmatogenous retinal detachment under silicone oil: case report and brief literature review.

IF 2.3 Q2 OPHTHALMOLOGY
Therapeutic Advances in Ophthalmology Pub Date : 2024-02-24 eCollection Date: 2024-01-01 DOI:10.1177/25158414241232261
Panagiotis Stavrakas, Foteini Tsapardoni, Efthymios Karmiris, Ioannis Iatropoulos, Konstantinos Kounas, Spyridon Lygeros, Vassilios Kozobolis, Demetrios G Vavvas
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Abstract

X-linked retinoschisis (XLRS) is an inherited retinal degeneration affecting males, characterized by splitting of the retinal layers. We herein present the outcomes of surgical treatment in a case of XLRS complicated by rhegmatogenous retinal detachment (RRD). A 22-year-old male presented to the emergency department due to decreased visual acuity and visual field defect in his left eye Oculus Sinister (OS) of 1 week duration. The patient reported an early onset retinal degeneration and decreased visual acuity in both eyes since childhood in his past ocular history. Upon presentation, best corrected visual acuity (BCVA) was 6/30 on the right eye Oculus Dexter (OD) and 6/120 OS. Fundus examination revealed areas of peripheral retinal schisis, and the characteristic spoke wheel pattern on the macula of both eyes. In OS, a temporal RRD involving the macula was identified. The patient underwent surgical treatment with pars plana vitrectomy with internal limiting membrane (ILM) peeling, endolaser, and silicone oil (SO) tamponade. BCVA in OS improved to 6/60 and schistic cavities resolution was observed in the immediate postoperative period. The patient's BCVA further improved to 6/19 at 1 month, as foveal anatomy showed relative improvement. However, there was a rapid reappearance of schisis spaces in the macular area at this point, which was also followed by progressive deterioration of foveal schisis by 3 months post-operatively. The resorption and recurrence of lamellar macular schisis changes after ILM peel and presence of SO, highlights that although XLRS findings can temporarily improve upon surgical intervention, the pathogenetic mechanisms contributing to disease phenotype remain to be elucidated.

在硅油条件下对流变性视网膜脱离行玻璃体切割术治疗的 X 连锁视网膜裂孔症黄斑裂孔早期复发:病例报告和简要文献综述。
X连锁视网膜裂孔症(XLRS)是一种遗传性视网膜变性,男性患者多见,其特点是视网膜层分裂。我们在此介绍一例XLRS并发流变性视网膜脱离(RRD)的手术治疗结果。一名 22 岁的男性因左眼视力下降和视野缺损(Oculus Sinister,OS)而到急诊科就诊,病程 1 周。患者称其过去的眼科病史中,双眼视网膜变性和视力下降自孩提时代就开始了。就诊时,他的右眼最佳矫正视力(BCVA)为 6/30,双眼最佳矫正视力(BCVA)为 6/120。眼底检查发现,双眼视网膜周围均有裂孔,黄斑部有特征性的辐状轮纹。在视网膜手术中,发现了累及黄斑的颞侧 RRD。患者接受了平面玻璃体旁切除术,并进行了内缘膜(ILM)剥离、内激光和硅油(SO)填塞等手术治疗。术后立即观察到OS的BCVA改善至6/60,裂孔消退。术后 1 个月,患者的 BCVA 进一步改善至 6/19,眼窝解剖结构也得到了相对改善。然而,此时黄斑区裂隙又迅速出现,术后 3 个月,眼窝裂隙也逐渐恶化。ILM剥离后片状黄斑裂孔变化的吸收和复发以及SO的存在,突出表明虽然XLRS结果在手术干预后可暂时改善,但导致疾病表型的致病机制仍有待阐明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.50
自引率
0.00%
发文量
44
审稿时长
12 weeks
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