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一种新型白瞳症分类法的提议。

Proposal of a novel classification of leukocorias.

作者信息

Tartarella Marcia Beatriz, Britez-Colombi Glória Fátima, Fortes Filho João Borges

机构信息

Department of Ophthalmology, Congenital Cataract Section, Federal University of São Paulo, São Paulo SP, Brazil.

出版信息

Clin Ophthalmol. 2012;6:991-5. doi: 10.2147/OPTH.S31469. Epub 2012 Jun 29.

DOI:10.2147/OPTH.S31469
PMID:22815641
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3399387/
Abstract

BACKGROUND

To report a case series of nine patients presenting with leukocoria without lens opacification or retrolental abnormalities and to propose a novel classification for leukocoria.

METHODS

An institutional and retrospective study including a case series of patients assisted in the Congenital Cataract Section of Federal University of São Paulo, Brazil, during the period between 2005 and 2010 with prelenticular leukocoria and clear lens.

RESULTS

Nine patients younger than 4 years old presented with the diagnosis of unilateral prelenticular opacities without cataract formation. Echography in all patients revealed no posterior segment or lens abnormalities in the affected eye. Among the patients, three had idiopathic prelenticular membrane, two presented with juvenile xanthogranuloma with secondary pupillary membrane, one had persistent fetal pupillary membrane, one had prelenticular membrane due to congenital toxoplasmosis, one presented with pupillary membrane due to hyphema caused by iris hemangioma, and one had anterior segment persistent fetal vasculature.

CONCLUSIONS

This case series of patients presented unilateral prelenticular leukocoria without lens opacification or posterior segment abnormalities. Several etiologies were associated with this condition. The correct diagnosis is important in order to avoid clear lens extraction. A new classification of leukocoria is proposed herein including: prelenticular leukocoria, lenticular leukocoria, retrolenticular leukocoria, and mixed presentation leukocoria.

摘要

背景

报告9例无晶状体混浊或晶状体后异常的白瞳症患者病例系列,并提出白瞳症的一种新分类。

方法

一项机构性回顾性研究,纳入2005年至2010年期间在巴西圣保罗联邦大学先天性白内障科就诊的一系列有晶状体前白瞳症且晶状体透明的患者。

结果

9例4岁以下患者被诊断为单侧晶状体前混浊且无白内障形成。所有患者的眼部超声检查均显示患眼后段或晶状体无异常。其中,3例为特发性晶状体前膜,2例为幼年性黄色肉芽肿伴继发性瞳孔膜,1例为永存胎儿瞳孔膜,1例为先天性弓形虫病所致晶状体前膜,1例为虹膜血管瘤引起的前房积血所致瞳孔膜,1例为前段永存胎儿血管。

结论

该病例系列患者表现为单侧晶状体前白瞳症,无晶状体混浊或后段异常。多种病因与该病症相关。正确诊断对于避免透明晶状体摘除很重要。本文提出白瞳症的一种新分类,包括:晶状体前白瞳症、晶状体性白瞳症、晶状体后白瞳症和混合性白瞳症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7617/3399387/b09c354fc7ee/opth-6-991f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7617/3399387/b09c354fc7ee/opth-6-991f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7617/3399387/b09c354fc7ee/opth-6-991f1.jpg

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