病理性近视后段表现综述

A. Elnahry
{"title":"病理性近视后段表现综述","authors":"A. Elnahry","doi":"10.19080/JOJO.2019.07.555709","DOIUrl":null,"url":null,"abstract":"Pathological myopia is a major cause of blindness worldwide that is becoming increasingly more prevalent in many countries of the world including Egypt [1,2]. Its exact cause is unknown; however, multiple genetic and environmental factors are thought to play a role in its complex pathogenesis [3]. The hallmark of pathological myopia is excessive and progressive axial length elongation which leads to degenerative changes in the sclera, choroid, and retinal pigment epithelium and compromises visual function [4,5]. Clinically, these changes include tessellated fundus, lacquer cracks, atrophy of the retinal pigment epithelium and choroid, choroidal neovascular membrane, posterior staphyloma, Fuchs’ spot, macular hole, foveoschisis, retinal breaks and detachments, and peripheral retinal lesions [6]. The effect of these manifestations on the visual performance of patients with pathological myopia can be substantial which emphasizes the value of the correct diagnosis and management of these complications. In this article, we review the clinical and morphological characteristics of the various posterior segment manifestations that can occur in pathological myopia as well as the value of multimodal imaging in the diagnosis and management of these manifestations.","PeriodicalId":91023,"journal":{"name":"JOJ ophthalmology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Posterior Segment Manifestations of Pathological Myopia: A Review\",\"authors\":\"A. Elnahry\",\"doi\":\"10.19080/JOJO.2019.07.555709\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Pathological myopia is a major cause of blindness worldwide that is becoming increasingly more prevalent in many countries of the world including Egypt [1,2]. Its exact cause is unknown; however, multiple genetic and environmental factors are thought to play a role in its complex pathogenesis [3]. The hallmark of pathological myopia is excessive and progressive axial length elongation which leads to degenerative changes in the sclera, choroid, and retinal pigment epithelium and compromises visual function [4,5]. Clinically, these changes include tessellated fundus, lacquer cracks, atrophy of the retinal pigment epithelium and choroid, choroidal neovascular membrane, posterior staphyloma, Fuchs’ spot, macular hole, foveoschisis, retinal breaks and detachments, and peripheral retinal lesions [6]. The effect of these manifestations on the visual performance of patients with pathological myopia can be substantial which emphasizes the value of the correct diagnosis and management of these complications. In this article, we review the clinical and morphological characteristics of the various posterior segment manifestations that can occur in pathological myopia as well as the value of multimodal imaging in the diagnosis and management of these manifestations.\",\"PeriodicalId\":91023,\"journal\":{\"name\":\"JOJ ophthalmology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-01-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"JOJ ophthalmology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.19080/JOJO.2019.07.555709\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"JOJ ophthalmology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.19080/JOJO.2019.07.555709","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

摘要

病理性近视是世界范围内致盲的主要原因,在包括埃及在内的世界许多国家越来越普遍[1,2]。其确切原因尚不清楚;然而,多种遗传和环境因素被认为在其复杂的发病机制中起作用。病理性近视的标志是过度和进行性的眼轴长度延长,导致巩膜、脉络膜和视网膜色素上皮的退行性改变,损害视觉功能[4,5]。临床表现为眼底镶嵌、漆膜裂纹、视网膜色素上皮及脉络膜萎缩、脉络膜新生血管膜、后葡萄肿、Fuchs斑、黄斑孔、凹裂、视网膜断裂及脱离、视网膜周围病变[6]。这些表现对病理性近视患者的视觉表现的影响可能是实质性的,这强调了正确诊断和处理这些并发症的价值。本文综述了病理性近视各种后段表现的临床和形态学特点,以及多模态成像在这些表现的诊断和治疗中的价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Posterior Segment Manifestations of Pathological Myopia: A Review
Pathological myopia is a major cause of blindness worldwide that is becoming increasingly more prevalent in many countries of the world including Egypt [1,2]. Its exact cause is unknown; however, multiple genetic and environmental factors are thought to play a role in its complex pathogenesis [3]. The hallmark of pathological myopia is excessive and progressive axial length elongation which leads to degenerative changes in the sclera, choroid, and retinal pigment epithelium and compromises visual function [4,5]. Clinically, these changes include tessellated fundus, lacquer cracks, atrophy of the retinal pigment epithelium and choroid, choroidal neovascular membrane, posterior staphyloma, Fuchs’ spot, macular hole, foveoschisis, retinal breaks and detachments, and peripheral retinal lesions [6]. The effect of these manifestations on the visual performance of patients with pathological myopia can be substantial which emphasizes the value of the correct diagnosis and management of these complications. In this article, we review the clinical and morphological characteristics of the various posterior segment manifestations that can occur in pathological myopia as well as the value of multimodal imaging in the diagnosis and management of these manifestations.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信