虹膜底结肠合并玻璃体出血及眼内肿块1例报告。

IF 0.3 Q4 OPHTHALMOLOGY
Punita Kumari Sodhi, Anu Sharma, Saurabh Verma, Ekta Shaw
{"title":"虹膜底结肠合并玻璃体出血及眼内肿块1例报告。","authors":"Punita Kumari Sodhi,&nbsp;Anu Sharma,&nbsp;Saurabh Verma,&nbsp;Ekta Shaw","doi":"10.3126/nepjoph.v14i1.39836","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Iridofundal colobomas, being developmental defects, are known to be accompanied by several ocular anomalies but an association with vitreous hemorrhage and an intraocular mass has not been reported earlier.</p><p><strong>Case: </strong>We report a case of an 18 years old subject having iridofundal coloboma in both eyes and an association of vitreous hemorrhage and an intraocular mass in the left eye. The diagnosis was confirmed with a detailed ocular examination, fundus fluorescein angiography, swept-source optical coherence tomography and ultrasonography. The laser barrage of coloboma caused a regression in the size of the intraocular mass and prevented recurrence of vitreous hemorrhage over one and half years of follow-up.</p><p><strong>Conclusion: </strong>The source of vitreous hemorrhage in this subject is unclear though some anomalous vessels in relation to the supero-nasal mass, optic disc and coloboma of the left eye might have caused it. The laser barrage of coloboma obscured these anomalous vessels resulting in the regression of the intraocular mass.</p>","PeriodicalId":44759,"journal":{"name":"Nepalese Journal of Ophthalmology","volume":null,"pages":null},"PeriodicalIF":0.3000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Iridofundal Coloboma Associated with Vitreous Haemorrhage and an Intraocular Mass: A Case Report.\",\"authors\":\"Punita Kumari Sodhi,&nbsp;Anu Sharma,&nbsp;Saurabh Verma,&nbsp;Ekta Shaw\",\"doi\":\"10.3126/nepjoph.v14i1.39836\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Iridofundal colobomas, being developmental defects, are known to be accompanied by several ocular anomalies but an association with vitreous hemorrhage and an intraocular mass has not been reported earlier.</p><p><strong>Case: </strong>We report a case of an 18 years old subject having iridofundal coloboma in both eyes and an association of vitreous hemorrhage and an intraocular mass in the left eye. The diagnosis was confirmed with a detailed ocular examination, fundus fluorescein angiography, swept-source optical coherence tomography and ultrasonography. The laser barrage of coloboma caused a regression in the size of the intraocular mass and prevented recurrence of vitreous hemorrhage over one and half years of follow-up.</p><p><strong>Conclusion: </strong>The source of vitreous hemorrhage in this subject is unclear though some anomalous vessels in relation to the supero-nasal mass, optic disc and coloboma of the left eye might have caused it. The laser barrage of coloboma obscured these anomalous vessels resulting in the regression of the intraocular mass.</p>\",\"PeriodicalId\":44759,\"journal\":{\"name\":\"Nepalese Journal of Ophthalmology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.3000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nepalese Journal of Ophthalmology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3126/nepjoph.v14i1.39836\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"OPHTHALMOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nepalese Journal of Ophthalmology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3126/nepjoph.v14i1.39836","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"OPHTHALMOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

虹膜底结肠瘤是一种发育缺陷,通常伴有几种眼部异常,但与玻璃体出血和眼内肿块相关的报道尚未见报道。病例:我们报告一例18岁的受试者,双眼虹膜基底结肠,并伴有玻璃体出血和左眼眼内肿块。通过详细的眼部检查、眼底荧光素血管造影、扫源光学相干断层扫描和超声检查证实了诊断。在一年半的随访中,激光轰击结肠瘤使眼内肿块的大小缩小,并防止玻璃体出血复发。结论:本例玻璃体出血的原因尚不清楚,可能与鼻上肿块、视盘及左眼结肠瘤有关的血管异常有关。结肠瘤的激光弹幕遮蔽了这些异常血管,导致眼内肿块消退。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Iridofundal Coloboma Associated with Vitreous Haemorrhage and an Intraocular Mass: A Case Report.

Introduction: Iridofundal colobomas, being developmental defects, are known to be accompanied by several ocular anomalies but an association with vitreous hemorrhage and an intraocular mass has not been reported earlier.

Case: We report a case of an 18 years old subject having iridofundal coloboma in both eyes and an association of vitreous hemorrhage and an intraocular mass in the left eye. The diagnosis was confirmed with a detailed ocular examination, fundus fluorescein angiography, swept-source optical coherence tomography and ultrasonography. The laser barrage of coloboma caused a regression in the size of the intraocular mass and prevented recurrence of vitreous hemorrhage over one and half years of follow-up.

Conclusion: The source of vitreous hemorrhage in this subject is unclear though some anomalous vessels in relation to the supero-nasal mass, optic disc and coloboma of the left eye might have caused it. The laser barrage of coloboma obscured these anomalous vessels resulting in the regression of the intraocular mass.

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
27
审稿时长
12 weeks
×
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