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色素失禁症的视网膜表现:14例病例系列,强调静脉荧光素血管造影的重要性及早期激光光凝治疗的益处

Retinal Manifestations of Incontinentia Pigmenti: A Case Series of 14 Patients Highlighting the Importance of Intravenous Fluorescein Angiography and the Benefits of Early Laser Photocoagulation.

作者信息

Bryan Jaimie, Issa Reda, Bakall Benjamin, Welch Matthew, Bryan J Shepard

机构信息

University of Florida College of Medicine, Gainesville, FL, USA.

Associated Retina Consultants, Phoenix, AZ, USA.

出版信息

J Vitreoretin Dis. 2020 Nov 3;5(1):60-65. doi: 10.1177/2474126420962645. eCollection 2021 Jan-Feb.

DOI:10.1177/2474126420962645
PMID:37009588
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9976039/
Abstract

PURPOSE

This case series describes the nature and frequency of retinal manifestations in patients with incontinentia pigmenti (IP).

METHODS

This is a retrospective single-center case series of all known patients with IP who presented to Associated Retina Consultants (Phoenix, AZ) between May 2016 and April 2019. Twenty-eight eyes of 14 patients with a dermatologic diagnosis of IP were included (n = 28). Most patients underwent examination under anesthesia with fundus photographs and intravenous fluorescein angiography (IVFA).

RESULTS

Of the 28 eyes, 8 (28.6%) had abnormal retinal findings on fundus examination. Of the 26 eyes that had IVFA, 10 (38.5%) had abnormal findings: Seven eyes (26.9%) had peripheral ischemia, 2 (7.7%) had previous peripheral laser scarring, and 2 (7.7%) had active peripheral neovascularization. Three eyes with normal examination results were found to have mild ischemia by IVFA. Patients with ischemia confirmed by IVFA were treated with laser photocoagulation. During follow-up, 4 previously treated eyes received additional laser photocoagulation. No patients showed vision loss, vitreous hemorrhage, retinal detachment, or adverse effects of treatment. No patients required vitreoretinal surgery.

CONCLUSIONS

IP is a potentially blinding disease. Our case series demonstrates the efficacy of early treatment and the importance of ancillary testing with IVFA and fundus photography.

摘要

目的

本病例系列描述色素失禁症(IP)患者视网膜表现的性质和频率。

方法

这是一项回顾性单中心病例系列研究,纳入了2016年5月至2019年4月期间就诊于联合视网膜顾问公司(亚利桑那州凤凰城)的所有已知IP患者。纳入了14例经皮肤科诊断为IP的患者的28只眼(n = 28)。大多数患者在麻醉下接受检查,并进行了眼底照相和静脉荧光素血管造影(IVFA)。

结果

在28只眼中,8只(28.6%)在眼底检查时有异常视网膜表现。在进行IVFA的26只眼中,10只(38.5%)有异常表现:7只眼(26.9%)有周边缺血,2只眼(7.7%)有既往周边激光瘢痕,2只眼(7.7%)有活动性周边新生血管形成。3只检查结果正常的眼经IVFA发现有轻度缺血。经IVFA确诊为缺血的患者接受了激光光凝治疗。在随访期间,4只先前接受治疗的眼接受了额外的激光光凝治疗。没有患者出现视力丧失、玻璃体积血、视网膜脱离或治疗不良反应。没有患者需要进行玻璃体视网膜手术。

结论

IP是一种潜在致盲性疾病。我们的病例系列证明了早期治疗的有效性以及IVFA和眼底照相辅助检查的重要性。

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本文引用的文献

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Acta Ophthalmol. 2019 May;97(3):265-272. doi: 10.1111/aos.13781. Epub 2018 Aug 3.
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Incontinentia Pigmenti: A Summary Review of This Rare Ectodermal Dysplasia With Neurologic Manifestations, Including Treatment Protocols.色素失禁症:这种伴有神经学表现的罕见外胚层发育不良的综述,包括治疗方案。
J Pediatr Health Care. 2017 Nov-Dec;31(6):e45-e52. doi: 10.1016/j.pedhc.2017.07.003. Epub 2017 Sep 1.
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New Insight Into the Pathogenesis of Cerebral Small-Vessel Diseases.对脑小血管病发病机制的新见解
Stroke. 2017 Feb;48(2):520-527. doi: 10.1161/STROKEAHA.116.012888. Epub 2017 Jan 12.
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Incontinentia pigmenti (Bloch-Sulzberger syndrome).色素失禁症(布洛赫-苏尔茨贝格综合征)。
Handb Clin Neurol. 2015;132:271-80. doi: 10.1016/B978-0-444-62702-5.00020-2.
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Incontinentia Pigmenti: A Comprehensive Review and Update.色素失禁症:全面综述与更新
Ophthalmic Surg Lasers Imaging Retina. 2015 Jun;46(6):650-7. doi: 10.3928/23258160-20150610-09.
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Extended Follow-up of Treated and Untreated Retinopathy in Incontinentia Pigmenti: Analysis of Peripheral Vascular Changes and Incidence of Retinal Detachment.未经治疗和治疗后的色素失禁症性视网膜病变的长期随访:外周血管变化分析及视网膜脱离的发生率。
JAMA Ophthalmol. 2015 May;133(5):542-8. doi: 10.1001/jamaophthalmol.2015.22.
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Systematic review of central nervous system anomalies in incontinentia pigmenti.先天性色素失禁症中枢神经系统异常的系统评价。
Orphanet J Rare Dis. 2013 Feb 13;8:25. doi: 10.1186/1750-1172-8-25.
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Ocular anomalies in incontinentia pigmenti: literature review and meta-analysis.色素失禁症的眼部异常:文献综述与荟萃分析
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