Cor triatriatum sinistrum in a Nigerian adult

A. Aje, O. Adebayo, Olugbenga Towoju, Opeyemi O. Oni, A. Adeoye, O. Ogah, A. Adebiyi, O. Oladapo
{"title":"Cor triatriatum sinistrum in a Nigerian adult","authors":"A. Aje, O. Adebayo, Olugbenga Towoju, Opeyemi O. Oni, A. Adeoye, O. Ogah, A. Adebiyi, O. Oladapo","doi":"10.4103/0189-7969.187729","DOIUrl":null,"url":null,"abstract":"Classical triatriatum sinistrum or cor triatriatum sinistrum is a rare congenital heart disorder arising from the left atrium being divided into two chambers and may present with undistinguishing features such as exertional dyspnea, hemoptysis, and orthopnea. It has been scarcely reported among adult Nigerians. The case being reported presented at an unusual age of 30 years. Most cases previously reported were in children. Definitive treatment is a corrective surgery with an excellent outcome. Nonintervention could have a catastrophic outcome. Therefore, there must be a high index of clinical suspicion and early diagnosis. This report is to increase awareness of such condition.","PeriodicalId":228906,"journal":{"name":"Nigerian Journal of Cardiology","volume":"200 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2016-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nigerian Journal of Cardiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/0189-7969.187729","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Classical triatriatum sinistrum or cor triatriatum sinistrum is a rare congenital heart disorder arising from the left atrium being divided into two chambers and may present with undistinguishing features such as exertional dyspnea, hemoptysis, and orthopnea. It has been scarcely reported among adult Nigerians. The case being reported presented at an unusual age of 30 years. Most cases previously reported were in children. Definitive treatment is a corrective surgery with an excellent outcome. Nonintervention could have a catastrophic outcome. Therefore, there must be a high index of clinical suspicion and early diagnosis. This report is to increase awareness of such condition.
尼日利亚成年人的三冠状核
典型的左心房三房综合征是一种罕见的先天性心脏疾病,由左心房分为两个腔室引起,可能表现为运动呼吸困难、咯血和直呼等不明显的特征。在尼日利亚成年人中几乎没有报道。报告的病例呈现在一个不寻常的年龄30岁。以前报告的大多数病例是儿童。最终的治疗方法是矫正手术,效果良好。不干预可能会带来灾难性的后果。因此,必须有较高的临床怀疑指数和早期诊断。这份报告是为了提高人们对这种情况的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
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:604180095
Book学术官方微信