法洛氏四联症婴儿肺动脉右冠状动脉异常。

IF 0.9 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS

Annals of Pediatric Cardiology Pub Date : 2023-11-01 Epub Date: 2024-04-23 DOI:10.4103/apc.apc_169_23

Swati Garekar, Ronak Sheth, Sachin Patil, Bharat Soni, Dhananjay P Malankar

{"title":"法洛氏四联症婴儿肺动脉右冠状动脉异常。","authors":"Swati Garekar, Ronak Sheth, Sachin Patil, Bharat Soni, Dhananjay P Malankar","doi":"10.4103/apc.apc_169_23","DOIUrl":null,"url":null,"abstract":"An anomalous right coronary artery from the pulmonary artery (ARCAPA) is a rare congenital anomaly that does not have the typical presentation of the more common anomalous left coronary artery. We present an infant with tetralogy of Fallot with atypical findings on the preoperative echocardiogram. A cardiac computerized tomographic (CT) scan showed ARCAPA. This was confirmed intraoperatively and repaired successfully. Close attention to coronaries on echocardiography and a low threshold for additional imaging can successfully diagnose ARCAPA in the presence of additional congenital heart defects.","PeriodicalId":8026,"journal":{"name":"Annals of Pediatric Cardiology","volume":null,"pages":null},"PeriodicalIF":0.9000,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11135895/pdf/","citationCount":"0","resultStr":"{\"title\":\"Anomalous right coronary artery from the pulmonary artery in an infant with tetralogy of Fallot.\",\"authors\":\"Swati Garekar, Ronak Sheth, Sachin Patil, Bharat Soni, Dhananjay P Malankar\",\"doi\":\"10.4103/apc.apc_169_23\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"An anomalous right coronary artery from the pulmonary artery (ARCAPA) is a rare congenital anomaly that does not have the typical presentation of the more common anomalous left coronary artery. We present an infant with tetralogy of Fallot with atypical findings on the preoperative echocardiogram. A cardiac computerized tomographic (CT) scan showed ARCAPA. This was confirmed intraoperatively and repaired successfully. Close attention to coronaries on echocardiography and a low threshold for additional imaging can successfully diagnose ARCAPA in the presence of additional congenital heart defects.\",\"PeriodicalId\":8026,\"journal\":{\"name\":\"Annals of Pediatric Cardiology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2023-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11135895/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annals of Pediatric Cardiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/apc.apc_169_23\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/4/23 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q4\",\"JCRName\":\"CARDIAC & CARDIOVASCULAR SYSTEMS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Pediatric Cardiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/apc.apc_169_23","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/4/23 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}

引用次数: 0

摘要

肺动脉右冠状动脉异常（ARCAPA）是一种罕见的先天性畸形，与更常见的左冠状动脉异常的典型表现不同。我们为您介绍一名在术前超声心动图检查中发现异常的法洛氏四联症婴儿。心脏计算机断层扫描（CT）显示其左冠状动脉有异常。术中证实了这一点，并成功进行了修复。密切关注超声心动图上的冠状动脉，并以较低的阈值进行其他成像检查，可以在存在其他先天性心脏缺陷的情况下成功诊断出 ARCAPA。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

Anomalous right coronary artery from the pulmonary artery in an infant with tetralogy of Fallot.

An anomalous right coronary artery from the pulmonary artery (ARCAPA) is a rare congenital anomaly that does not have the typical presentation of the more common anomalous left coronary artery. We present an infant with tetralogy of Fallot with atypical findings on the preoperative echocardiogram. A cardiac computerized tomographic (CT) scan showed ARCAPA. This was confirmed intraoperatively and repaired successfully. Close attention to coronaries on echocardiography and a low threshold for additional imaging can successfully diagnose ARCAPA in the presence of additional congenital heart defects.

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

Annals of Pediatric Cardiology CARDIAC & CARDIOVASCULAR SYSTEMS-

CiteScore

1.40

自引率

14.30%

发文量

审稿时长

23 weeks