{"title":"新生儿巨大右心房附件动脉瘤成功治疗:一例罕见病例报告","authors":"Sudipta Bandyopadhyay , Swaminathan Vaidyanathan , C.S. Muthukumaran , Neville Solomon","doi":"10.1016/j.ppedcard.2023.101661","DOIUrl":null,"url":null,"abstract":"<div><p><span>A right atrial appendage aneurysm is an extremely rare cardiac anomaly. According to the literature, so far, 10 cases have been detected in pediatric populations. A very small number of cases have so far undergone surgical repair in the </span>newborn period<span><span><span><span><span>. It can be asymptomatic or may be associated with arrhythmia or right heart failure. Here we are presenting a case of a </span>newborn<span> with a giant right atrial appendage aneurysm, arrhythmia, and mild respiratory distress. The aneurysm was diagnosed by transthoracic echocardiography and confirmed by a cardiac </span></span>CT scan. It was resected surgically under </span>cardiopulmonary bypass. Postoperatively, the baby was extubated on the 2nd postoperative day and discharged on the 7th postoperative day. Because of its rare occurrence, diagnosis is sometimes difficult, and it may be confused with the </span>Ebstein anomaly.</span></p></div>","PeriodicalId":46028,"journal":{"name":"PROGRESS IN PEDIATRIC CARDIOLOGY","volume":null,"pages":null},"PeriodicalIF":0.6000,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Giant right atrial appendage aneurysm successfully managed in a newborn: A rare case report\",\"authors\":\"Sudipta Bandyopadhyay , Swaminathan Vaidyanathan , C.S. Muthukumaran , Neville Solomon\",\"doi\":\"10.1016/j.ppedcard.2023.101661\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span>A right atrial appendage aneurysm is an extremely rare cardiac anomaly. According to the literature, so far, 10 cases have been detected in pediatric populations. A very small number of cases have so far undergone surgical repair in the </span>newborn period<span><span><span><span><span>. It can be asymptomatic or may be associated with arrhythmia or right heart failure. Here we are presenting a case of a </span>newborn<span> with a giant right atrial appendage aneurysm, arrhythmia, and mild respiratory distress. The aneurysm was diagnosed by transthoracic echocardiography and confirmed by a cardiac </span></span>CT scan. It was resected surgically under </span>cardiopulmonary bypass. Postoperatively, the baby was extubated on the 2nd postoperative day and discharged on the 7th postoperative day. Because of its rare occurrence, diagnosis is sometimes difficult, and it may be confused with the </span>Ebstein anomaly.</span></p></div>\",\"PeriodicalId\":46028,\"journal\":{\"name\":\"PROGRESS IN PEDIATRIC CARDIOLOGY\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.6000,\"publicationDate\":\"2023-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"PROGRESS IN PEDIATRIC CARDIOLOGY\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1058981323000498\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"PEDIATRICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"PROGRESS IN PEDIATRIC CARDIOLOGY","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1058981323000498","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PEDIATRICS","Score":null,"Total":0}
Giant right atrial appendage aneurysm successfully managed in a newborn: A rare case report
A right atrial appendage aneurysm is an extremely rare cardiac anomaly. According to the literature, so far, 10 cases have been detected in pediatric populations. A very small number of cases have so far undergone surgical repair in the newborn period. It can be asymptomatic or may be associated with arrhythmia or right heart failure. Here we are presenting a case of a newborn with a giant right atrial appendage aneurysm, arrhythmia, and mild respiratory distress. The aneurysm was diagnosed by transthoracic echocardiography and confirmed by a cardiac CT scan. It was resected surgically under cardiopulmonary bypass. Postoperatively, the baby was extubated on the 2nd postoperative day and discharged on the 7th postoperative day. Because of its rare occurrence, diagnosis is sometimes difficult, and it may be confused with the Ebstein anomaly.
期刊介绍:
Progress in Pediatric Cardiology is an international journal of review presenting information and experienced opinion of importance in the understanding and management of cardiovascular diseases in children. Each issue is prepared by one or more Guest Editors and reviews a single subject, allowing for comprehensive presentations of complex, multifaceted or rapidly changing topics of clinical and investigative interest.