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Anomalous origin of a pulmonary artery in a teenager with tetralogy of Fallot with associated double aortic arch and coronary arteriovenous fistula

Part of: Tetralogy of Fallot (TOF) Cardiac Morphology

Published online by Cambridge University Press:  28 May 2019

Vishal Agrawal ,
Parth Solanki ,
Ritesh Shah ,
Divyakant Parmar  and
Amit Mishra
Vishal Agrawal
Affiliation:
Department of Cardiovascular and Thoracic Surgery, U.N. Mehta Institute of Cardiology and Research Center (affiliated to B.J. Medical College, Ahmedabad), Civil Hospital Campus, Asarwa, Ahmedabad 380016, India
Parth Solanki
Affiliation:
Department of Cardiovascular and Thoracic Surgery, U.N. Mehta Institute of Cardiology and Research Center (affiliated to B.J. Medical College, Ahmedabad), Civil Hospital Campus, Asarwa, Ahmedabad 380016, India
Ritesh Shah
Affiliation:
Department of Cardiac Anaesthesia, U.N. Mehta Institute of Cardiology and Research Center (affiliated to B.J. Medical College, Ahmedabad), Civil Hospital Campus, Asarwa, Ahmedabad 380016, India
Divyakant Parmar
Affiliation:
Department of Cardiac Anaesthesia, U.N. Mehta Institute of Cardiology and Research Center (affiliated to B.J. Medical College, Ahmedabad), Civil Hospital Campus, Asarwa, Ahmedabad 380016, India
Amit Mishra*
Affiliation:
Department of Pediatric Cardiovascular and Thoracic Surgery, U.N. Mehta Institute of Cardiology and Research Center (affiliated to B.J. Medical College, Ahmedabad), Civil Hospital Campus, Asarwa, Ahmedabad 380016, India
*
Author for correspondence: Dr. Amit Mishra, Department of Cardiovascular and Thoracic Surgery, U.N. Mehta Institute of Cardiology and Research Center (affiliated to B.J. Medical College), New Civil Hospital Campus, Asarwa, Ahmedabad 380016, Gujarat, India. Tel: 91-09979203994; E-mail: [email protected]
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Abstract

We report the case of a 14-year-old female who had tetralogy of Fallot along with anomalous origin of the left pulmonary artery from the ascending aorta with co-dominant double aortic arch forming a complete vascular ring compressing the oesophagus along with a left main coronary artery to right ventricular outflow tract fistula. She underwent surgical correction without conduit placement.

Keywords

Anomalous origin of a pulmonary arterytetralogy of fallotright ventricular outflow tract
Type
Brief Report
Information
Cardiology in the Young , Volume 29 , Issue 5 , May 2019 , pp. 727 - 729
Copyright
© Cambridge University Press 2019 

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