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Double aortic arch in a newborn with congenital diaphragmatic hernia and tracheoesophageal fistula

Published online by Cambridge University Press:  28 April 2014

Joanne S. Chiu ,
Julie Glickstein  and
Amee Shah
Joanne S. Chiu
Affiliation:
Department of Pediatrics, Division of Cardiology, Columbia University Medical Center, New York, New York, United States of America
Julie Glickstein
Affiliation:
Department of Pediatrics, Division of Cardiology, Columbia University Medical Center, New York, New York, United States of America
Amee Shah*
Affiliation:
Department of Pediatrics, Division of Cardiology, Columbia University Medical Center, New York, New York, United States of America
*
Correspondence to: A. Shah, Department of Pediatrics, Division of Cardiology, Columbia University Medical Center, 3959 Broadway, 2-Babies North, New York, New York 10032, United States of America. Tel: +212 342 1560; Fax: +212 305 4429; E-mail: ams79@columbia.edu
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Abstract

Congenital heart disease is associated with congenital diaphragmatic hernia, but diagnosis by echocardiography can be difficult. We present the unusual case of a patient with a double aortic arch and congenital diaphragmatic hernia diagnosed using cardiac magnetic resonance imaging.

Keywords

Double aortic archcongenital diaphragmatic herniacardiac magnetic resonance
Type
Images in Congenital Cardiac Disease
Information
Cardiology in the Young , Volume 24 , Issue 4 , August 2014 , pp. 725 - 726
Copyright
© Cambridge University Press 2014 

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References

1. Wynn, J, Krishnan, U, Aspelund, G, et al. Outcomes of congenital diaphragmatic hernia in the modern era of management. J Pediatr 2013; 163: 114–119.Google Scholar