Case of anomalous origin of right coronary artery from pulmonary artery associated with interrupted aortic arch type A, diagnosed by multidetector computed tomography angiography

Anomalous origin of the right coronary artery from pulmonary artery (ARCAPA) is a rare congenital anomaly of the coronary circulation, which can be easily missed by echocardiography. Interrupted aortic arch (IAA) is another rare congenital cardiac abnormality that typically presents in the first few...

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Main Authors: Neetu Soni, Sunil Kumar Jain, Anil Kumar, Renu Kadian, Shou Li
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2019-01-01
Series:Annals of Pediatric Cardiology
Subjects:
Online Access:http://www.annalspc.com/article.asp?issn=0974-2069;year=2019;volume=12;issue=3;spage=345;epage=347;aulast=Soni
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spelling doaj-99135c806a7d45c7a81ccef8be17a68a2020-11-24T21:27:24ZengWolters Kluwer Medknow PublicationsAnnals of Pediatric Cardiology0974-20692019-01-0112334534710.4103/apc.APC_69_18Case of anomalous origin of right coronary artery from pulmonary artery associated with interrupted aortic arch type A, diagnosed by multidetector computed tomography angiographyNeetu SoniSunil Kumar JainAnil KumarRenu KadianShou LiAnomalous origin of the right coronary artery from pulmonary artery (ARCAPA) is a rare congenital anomaly of the coronary circulation, which can be easily missed by echocardiography. Interrupted aortic arch (IAA) is another rare congenital cardiac abnormality that typically presents in the first few weeks of life. We present a case of ARCAPA associated with IAA diagnosed with the help of multidetector computed tomography angiography, in a 7-year-old boy.http://www.annalspc.com/article.asp?issn=0974-2069;year=2019;volume=12;issue=3;spage=345;epage=347;aulast=SoniAnomalous origin of the right coronary artery from pulmonary arteryinterrupted aortic archmultidetector computed tomography angiography
collection DOAJ
language English
format Article
sources DOAJ
author Neetu Soni
Sunil Kumar Jain
Anil Kumar
Renu Kadian
Shou Li
spellingShingle Neetu Soni
Sunil Kumar Jain
Anil Kumar
Renu Kadian
Shou Li
Case of anomalous origin of right coronary artery from pulmonary artery associated with interrupted aortic arch type A, diagnosed by multidetector computed tomography angiography
Annals of Pediatric Cardiology
Anomalous origin of the right coronary artery from pulmonary artery
interrupted aortic arch
multidetector computed tomography angiography
author_facet Neetu Soni
Sunil Kumar Jain
Anil Kumar
Renu Kadian
Shou Li
author_sort Neetu Soni
title Case of anomalous origin of right coronary artery from pulmonary artery associated with interrupted aortic arch type A, diagnosed by multidetector computed tomography angiography
title_short Case of anomalous origin of right coronary artery from pulmonary artery associated with interrupted aortic arch type A, diagnosed by multidetector computed tomography angiography
title_full Case of anomalous origin of right coronary artery from pulmonary artery associated with interrupted aortic arch type A, diagnosed by multidetector computed tomography angiography
title_fullStr Case of anomalous origin of right coronary artery from pulmonary artery associated with interrupted aortic arch type A, diagnosed by multidetector computed tomography angiography
title_full_unstemmed Case of anomalous origin of right coronary artery from pulmonary artery associated with interrupted aortic arch type A, diagnosed by multidetector computed tomography angiography
title_sort case of anomalous origin of right coronary artery from pulmonary artery associated with interrupted aortic arch type a, diagnosed by multidetector computed tomography angiography
publisher Wolters Kluwer Medknow Publications
series Annals of Pediatric Cardiology
issn 0974-2069
publishDate 2019-01-01
description Anomalous origin of the right coronary artery from pulmonary artery (ARCAPA) is a rare congenital anomaly of the coronary circulation, which can be easily missed by echocardiography. Interrupted aortic arch (IAA) is another rare congenital cardiac abnormality that typically presents in the first few weeks of life. We present a case of ARCAPA associated with IAA diagnosed with the help of multidetector computed tomography angiography, in a 7-year-old boy.
topic Anomalous origin of the right coronary artery from pulmonary artery
interrupted aortic arch
multidetector computed tomography angiography
url http://www.annalspc.com/article.asp?issn=0974-2069;year=2019;volume=12;issue=3;spage=345;epage=347;aulast=Soni
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