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

Authors

Neetu Soni, Department of Radiology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Sunil Kumar Jain, Department of Radiology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Anil Kumar, Department of Neurology, Great Plains Health, North Platte, Nebraska, USA.
Renu Kadian, Department of Medicine, Great Plains Health, North Platte, Nebraska, USA.
Shou Li, Department of Radiology, YaleNew Haven Health Bridgeport Hospital, Bridgeport, Connecticut, USA.

Document Type

Article

Publication Title

Annals of pediatric cardiology

Abstract

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.

First Page

345

Last Page

347

DOI

10.4103/apc.APC_69_18

Publication Date

1-1-2019

Recommended Citation

Soni, Neetu; Jain, Sunil Kumar; Kumar, Anil; Kadian, Renu; and Li, Shou, "Case of anomalous origin of right coronary artery from pulmonary artery associated with interrupted aortic arch type A, diagnosed by multidetector computed tomography angiography" (2019). Radiology. 114.
https://scholar.bridgeporthospital.org/radiology/114

Identifier

31516301 (pubmed); PMC6716321 (pmc); 10.4103/apc.APC_69_18 (doi); APC-12-345 (pii)