Year : 2019  |  Volume : 12  |  Issue : 3  |  Page : 345--347

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


Neetu Soni1, Sunil Kumar Jain1, Anil Kumar2, Renu Kadian3, Shou Li4 
1 Department of Radiology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India
2 Department of Neurology, Great Plains Health, North Platte, Nebraska, USA
3 Department of Medicine, Great Plains Health, North Platte, Nebraska, USA
4 Department of Radiology, YaleNew Haven Health Bridgeport Hospital, Bridgeport, Connecticut, USA

Correspondence Address:
Dr. Anil Kumar
Department of Neurology, Great Plains Health North Platte, Nebraska
USA

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.


How to cite this article:
Soni N, Jain SK, Kumar A, Kadian R, Li S. Case of anomalous origin of right coronary artery from pulmonary artery associated with interrupted aortic arch type A, diagnosed by multidetector computed tomography angiography.Ann Pediatr Card 2019;12:345-347


How to cite this URL:
Soni N, Jain SK, Kumar A, Kadian R, Li S. Case of anomalous origin of right coronary artery from pulmonary artery associated with interrupted aortic arch type A, diagnosed by multidetector computed tomography angiography. Ann Pediatr Card [serial online] 2019 [cited 2020 Oct 31 ];12:345-347
Available from: https://www.annalspc.com/article.asp?issn=0974-2069;year=2019;volume=12;issue=3;spage=345;epage=347;aulast=Soni;type=0