David Brieger FRACP , Thavaraja Singham FRACP , David Richmond FRACP , Duncan Thomson FRACS
{"title":"Cor triatriatum and rheumatic mitral stenosis in adulthood: Assessment of combined congenital and acquired cardiac disease in a 60-year-old woman","authors":"David Brieger FRACP , Thavaraja Singham FRACP , David Richmond FRACP , Duncan Thomson FRACS","doi":"10.1016/1324-2881(95)90046-2","DOIUrl":null,"url":null,"abstract":"<div><p>Cor triatriatum is a congenital anomaly rarely described in adults. It causes left ventricular inflow obstruction and mimics mitral stenosis. The 2 conditions have rarely been reported concurrently. This report describes the case of a 60-year-old women with rheumatic mitral stenosis and single vessel coronary disease, in whom cor triatriatum was diagnosed coincidentally at echocardiography. All lesions were successfully managed by surgery.</p></div>","PeriodicalId":101219,"journal":{"name":"The Asia Pacific Journal of Thoracic & Cardiovascular Surgery","volume":"4 2","pages":"Pages 78-80"},"PeriodicalIF":0.0000,"publicationDate":"1995-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/1324-2881(95)90046-2","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Asia Pacific Journal of Thoracic & Cardiovascular Surgery","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/1324288195900462","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
Cor triatriatum is a congenital anomaly rarely described in adults. It causes left ventricular inflow obstruction and mimics mitral stenosis. The 2 conditions have rarely been reported concurrently. This report describes the case of a 60-year-old women with rheumatic mitral stenosis and single vessel coronary disease, in whom cor triatriatum was diagnosed coincidentally at echocardiography. All lesions were successfully managed by surgery.