• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

永存原始玻璃体增生症:眼部特征、白内障的治疗及预后

Persistent fetal vasculature: ocular features, management of cataract and outcomes.

作者信息

Tartarella Marcia Beatriz, Takahagi Rodrigo Ueno, Braga Ana Paula, Fortes Filho João Borges

机构信息

Department of Ophthalmology, School of Medicine, Universidade Federal de São Paulo, São Paulo (SP), Brazil.

出版信息

Arq Bras Oftalmol. 2013 May-Jun;76(3):185-8. doi: 10.1590/s0004-27492013000300011.

DOI:10.1590/s0004-27492013000300011
PMID:23929081
Abstract

PURPOSES

To describe ocular features, management of cataract and functional outcomes in patients with persistent fetal vasculature.

METHODS

Retrospective, descriptive case series of patients with persistent fetal vasculature. Data were recorded from the Congenital Cataract Section of Federal University of São Paulo, Brazil from 2001 to 2012. All patients were evaluated for sex, age at diagnosis, systemic findings, laterality, age at surgery, and initial and final follow-up visual acuities. Follow-up and complications after cataract surgery were recorded. Ultrasound was performed in all cases and ocular eco-Doppler was performed in most.

RESULTS

The study comprised 53 eyes from 46 patients. Age at diagnosis ranged from 5 days of life to 10 years-old (mean 22.7 months). Twenty-seven patients were male (58.7%). Persistent fetal vasculature was bilateral in 7 patients (15.2%). Forty-two eyes (79.2%) had combined (anterior and posterior forms) PFV presentation, 5 eyes (9.4%) had only anterior persistent fetal vasculature presentation and 6 eyes (11.3%) had posterior persistent fetal vasculature presentation. Thirty-eight eyes (71.7%) were submitted to cataract surgery. Lensectomy combined with anterior vitrectomy was performed in 18 eyes (47.4%). Phacoaspiration with intraocular lens implantation was performed in 15 eyes (39.5%), and without lens implantation in 5 eyes (13.2%). Mean follow-up after surgery was 44 months. Postoperative complications were posterior synechiae (3 cases), retinal detachment (2 cases), phthisis (3 cases), posterior capsular opacification (8 cases), inflammatory pupillary membrane (5 cases), glaucoma (4 cases), intraocular lens implantation displacement (1 case) and vitreous hemorrhage (2 cases). Complications were identified in 19 (50%) of the 38 operated eyes. Visual acuity improved after cataract surgery in 83% of the eyes.

CONCLUSIONS

Patients with persistent fetal vasculature have variable clinical presentation. There is an association of persistent fetal vasculature with congenital cataract. Severe complications are related to cataract surgery in patients with persistent fetal vasculature, but 83% of the operated eyes improved visual acuity.

摘要

目的

描述永存原始玻璃体增生症患者的眼部特征、白内障治疗方法及功能预后。

方法

对永存原始玻璃体增生症患者进行回顾性描述性病例系列研究。数据来自巴西圣保罗联邦大学先天性白内障科室2001年至2012年期间的病例。对所有患者的性别、诊断时年龄、全身检查结果、病变眼别、手术年龄以及初次和末次随访视力进行评估。记录白内障手术后的随访情况及并发症。所有病例均进行了超声检查,大多数病例还进行了眼部彩色多普勒超声检查。

结果

该研究纳入了46例患者的53只眼。诊断时年龄范围为出生5天至10岁(平均22.7个月)。27例患者为男性(58.7%)。7例患者(15.2%)的永存原始玻璃体增生症为双眼病变。42只眼(79.2%)表现为联合型(前部和后部型)永存原始玻璃体增生症,5只眼(9.4%)仅表现为前部永存原始玻璃体增生症,6只眼(11.3%)表现为后部永存原始玻璃体增生症。38只眼(71.7%)接受了白内障手术。18只眼(47.4%)进行了晶状体切除术联合前部玻璃体切除术。15只眼(39.5%)进行了超声乳化白内障吸除联合人工晶状体植入术,5只眼(13.2%)未植入人工晶状体。手术后平均随访44个月。术后并发症包括虹膜后粘连(3例)、视网膜脱离(2例)、眼球痨(3例)、后囊膜混浊(8例)、炎性瞳孔膜(5例)、青光眼(4例)、人工晶状体植入移位(1例)和玻璃体积血(2例)。38只手术眼中有19只眼(50%)出现了并发症。白内障手术后83%的患眼视力得到改善。

结论

永存原始玻璃体增生症患者临床表现多样。永存原始玻璃体增生症与先天性白内障有关。永存原始玻璃体增生症患者白内障手术相关的严重并发症较多,但83%的手术患眼视力得到改善。

相似文献

1
Persistent fetal vasculature: ocular features, management of cataract and outcomes.永存原始玻璃体增生症:眼部特征、白内障的治疗及预后
Arq Bras Oftalmol. 2013 May-Jun;76(3):185-8. doi: 10.1590/s0004-27492013000300011.
2
Congenital cataract surgery without intraocular lens implantation in persistent fetal vasculature syndrome: Long-term clinical and functional results.持续性胎儿血管综合征中无人工晶状体植入的先天性白内障手术:长期临床和功能结果
J Cataract Refract Surg. 2016 May;42(5):759-67. doi: 10.1016/j.jcrs.2016.02.040.
3
Outcomes of cataract surgery in children with persistent hyperplastic primary vitreous.永存原始玻璃体增生症患儿白内障手术的结局
Eur J Ophthalmol. 2018 Mar;28(2):193-197. doi: 10.5301/ejo.5001017. Epub 2017 Sep 14.
4
Persistent Fetal Vasculature With Elongated Ciliary Processes in Children.儿童永存胎儿血管伴睫状突细长
Am J Ophthalmol. 2019 Feb;198:25-29. doi: 10.1016/j.ajo.2018.09.019. Epub 2018 Sep 27.
5
Risk factors for complications after congenital cataract surgery without intraocular lens implantation in the first 18 months of life.出生后18个月内未植入人工晶状体的先天性白内障手术后并发症的危险因素。
Am J Ophthalmol. 2008 Jul;146(1):1-7. doi: 10.1016/j.ajo.2008.02.014. Epub 2008 Apr 14.
6
Visual and anatomic outcomes with or without surgery in persistent fetal vasculature.持续性胎儿血管中手术与非手术的视觉和解剖结果。
Ophthalmology. 2010 Nov;117(11):2178-83.e1-2. doi: 10.1016/j.ophtha.2010.03.062.
7
Functional and anatomical outcomes following surgical management of persistent fetal vasculature: a single-center experience of 44 cases.持续性胎儿血管系统手术治疗后的功能和解剖学结果:44例单中心经验
Graefes Arch Clin Exp Ophthalmol. 2018 Mar;256(3):495-501. doi: 10.1007/s00417-017-3886-4. Epub 2018 Jan 3.
8
Primary intraocular lens implantation in infants: complications and visual results.婴儿期一期人工晶状体植入:并发症及视觉效果
J Cataract Refract Surg. 2006 Oct;32(10):1672-7. doi: 10.1016/j.jcrs.2006.05.004.
9
Visual acuity outcomes with and without surgery in patients with persistent fetal vasculature.永存原始玻璃体增生症患者手术与非手术治疗后的视力结果。
Ophthalmology. 2000 Jun;107(6):1068-72. doi: 10.1016/s0161-6420(00)00100-7.
10
Outcomes of pediatric cataract surgery in anterior persistent fetal vasculature.儿童白内障手术在前持续性胎儿血管中的结果。
J Cataract Refract Surg. 2012 May;38(5):849-57. doi: 10.1016/j.jcrs.2011.11.045.

引用本文的文献

1
Surgical Parameters and Prognostic Factors in Persistent Fetal Vasculature: Insights from a Retrospective Cohort Study.持续性胎儿血管系统的手术参数和预后因素:一项回顾性队列研究的见解
Ophthalmol Ther. 2025 Mar;14(3):515-528. doi: 10.1007/s40123-024-01088-6. Epub 2025 Jan 15.
2
Retrospective Analysis of Surgical Outcomes on Axial Length Elongation in Eyes with Posterior and Combined Persistent Fetal Vasculature.后极部和联合永存原始玻璃体血管病变眼的眼轴延长手术效果的回顾性分析。
Int J Mol Sci. 2023 Mar 19;24(6):5836. doi: 10.3390/ijms24065836.
3
Current management of infantile cataracts.
婴幼儿白内障的现行治疗方法。
Surv Ophthalmol. 2022 Sep-Oct;67(5):1476-1505. doi: 10.1016/j.survophthal.2022.03.005. Epub 2022 Mar 17.
4
Outcomes and surgical management of persistent fetal vasculature.持续性胎儿血管系统的治疗结果及手术管理
BMJ Open Ophthalmol. 2021 Apr 29;6(1):e000656. doi: 10.1136/bmjophth-2020-000656. eCollection 2021.
5
Clinical characteristics of morning glory disc anomaly in South India.印度南部牵牛花盘状异常的临床特征。
Taiwan J Ophthalmol. 2020 Oct 19;11(1):57-63. doi: 10.4103/tjo.tjo_52_20. eCollection 2021 Jan-Mar.
6
Diagnostic and Management Strategies in Patients with Persistent Fetal Vasculature: Current Insights.持续性胎儿血管患者的诊断与管理策略:当前见解
Clin Ophthalmol. 2020 Dec 10;14:4325-4335. doi: 10.2147/OPTH.S236117. eCollection 2020.
7
Clinical Characteristics and Surgical Safety in Congenital Cataract Eyes with Three Pathological Types of Posterior Capsule Abnormalities.具有三种后囊异常病理类型的先天性白内障眼的临床特征及手术安全性
J Ophthalmol. 2020 Mar 16;2020:6958051. doi: 10.1155/2020/6958051. eCollection 2020.
8
Regression of fetal vasculature and visual improvement in nonsurgical persistent hyperplastic primary vitreous: a case report.非手术性持续性增生性原发性玻璃体病变中胎儿血管的消退及视力改善:一例报告
BMC Ophthalmol. 2019 Jul 26;19(1):161. doi: 10.1186/s12886-019-1173-3.
9
Management of severe persistent fetal vasculature: case series and review of the literature.重度持续性胎儿血管系统的管理:病例系列及文献综述
Int Ophthalmol. 2019 Mar;39(3):579-587. doi: 10.1007/s10792-018-0855-9. Epub 2018 Feb 23.
10
Unilateral anterior persistent fetal vasculature in a child with blepharophimosis-ptosis-epicanthus inversus syndrome: A surgical challenge.患有睑裂狭小-上睑下垂-内眦赘皮综合征儿童的单侧前部永存胎儿血管:一项手术挑战。
Indian J Ophthalmol. 2016 Jun;64(6):469-71. doi: 10.4103/0301-4738.187681.