Barresi Costanza, Chapron Thibaut, Chehaibou Ismael, Metge Florence, Caputo Georges, Abdelmassih Youssef
Department of Pediatric Ophthalmology and Retina, Rothschild Foundation Hospital, 25 rue Manin, Paris-Cedex 19, 75940, France.
Vita-Salute San Raffaele University, Milan, Italy.
Graefes Arch Clin Exp Ophthalmol. 2025 Jun 11. doi: 10.1007/s00417-025-06871-0.
To evaluate surgical and visual outcomes following retinal detachment (RD) repair after lensectomy in pediatric patients with Marfan syndrome.
This retrospective cohort study included patients under 21 years of age with Marfan syndrome who RD following lensectomy for ectopia lentis between January 2011 and January 2024. All patients underwent a comprehensive ophthalmologic assessment at baseline, defined as the visit at which RD was diagnosed, as well as at follow-up visits. Data were collected on clinical features of RD, anatomical success rates, complications, and changes in visual outcomes after surgery.
A total of 33 eyes from 25 patients (18 males, 72%) with a mean age at presentation of 12.6 ± 4.7 years were included. The mean axial length was 27.8 ± 2.8 mm, and the mean postoperative follow-up duration was 6.1 ± 5.8 years. The most common RD mechanisms were horseshoe tears (33%), retinal holes (33%), and giant retinal tears (15%). Fifteen eyes underwent scleral buckle (SB) surgery as the initial procedure (45.5%), 10 underwent pars plana vitrectomy (PPV) alone (30.3%), and 8 underwent combined PPV and SB surgery (24.2%). Complete anatomical success was achieved in 73.0% (24 eyes) of cases: after one surgery in 16 eyes (67%), two surgeries in 6 eyes (25%), and three surgeries in 2 eyes (8%). An additional 12% (4 eyes) remained attached under silicone oil tamponade at final follow-up. Only the presence of proliferative vitreoretinopathy (PVR) was associated with a lower success rate (p = 0.001). Visual acuity significantly improved after surgery (1.7 ± 1.3 LogMAR vs. 0.8 ± 1.1; p < 0.001). Postoperative complications included ocular hypertension (27.3%), corneal edema (18.2%), and cystoid macular edema (9.1%).
Surgical management of RD following lensectomy in pediatric patients with Marfan syndrome remains challenging but is indicated, as it can provide meaningful visual improvement and anatomical stabilization in a subset of cases. The presence of PVR affects both surgical outcomes and the number of surgeries required.
评估马凡综合征小儿患者晶状体切除术后视网膜脱离(RD)修复后的手术及视觉效果。
这项回顾性队列研究纳入了2011年1月至2024年1月期间因晶状体异位行晶状体切除术后发生RD的21岁以下马凡综合征患者。所有患者在基线时(定义为诊断出RD的就诊时)以及随访时均接受了全面的眼科评估。收集了RD的临床特征、解剖成功率、并发症以及手术后视觉效果变化的数据。
共纳入25例患者(18例男性,72%)的33只眼,平均就诊年龄为12.6±4.7岁。平均眼轴长度为27.8±2.8mm,术后平均随访时间为6.1±5.8年。最常见的RD机制是马蹄形裂孔(33%)、视网膜裂孔(33%)和巨大视网膜裂孔(15%)。15只眼最初接受巩膜扣带术(SB)(45.5%),10只眼仅接受玻璃体切割术(PPV)(30.3%),8只眼接受PPV联合SB手术(24.2%)。73.0%(24只眼)的病例实现了完全解剖成功:16只眼(67%)一次手术后成功,6只眼(25%)两次手术后成功,2只眼(8%)三次手术后成功。在最后一次随访时,另有12%(4只眼)在硅油填充下保持视网膜附着。仅增殖性玻璃体视网膜病变(PVR)的存在与较低的成功率相关(p = 0.001)。术后视力显著改善(术前1.7±1.3 LogMAR,术后0.8±1.1;p < 0.001)。术后并发症包括高眼压(27.3%)、角膜水肿(18.2%)和黄斑囊样水肿(9.1%)。
马凡综合征小儿患者晶状体切除术后RD的手术治疗仍然具有挑战性,但仍有必要进行,因为它可以在一部分病例中提供有意义的视力改善和解剖稳定。PVR的存在会影响手术效果和所需的手术次数。