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Aortic coarctation, aneurysm, and ventricular dysfunction in an asymptomatic infant

Published online by Cambridge University Press:  16 March 2016

Ana I. García ,
Juan M. Aguilar  and
Enrique García
Ana I. García
Affiliation:
Department of Pediatric Cardiac Surgery, Pediatric Heart Institute, Hospital Universitario Doce de Octubre, Madrid, España
Juan M. Aguilar*
Affiliation:
Department of Pediatric Cardiac Surgery, Pediatric Heart Institute, Hospital Universitario Doce de Octubre, Madrid, España
Enrique García
Affiliation:
Department of Pediatric Cardiac Surgery, Pediatric Heart Institute, Hospital Universitario Doce de Octubre, Madrid, España
*
Correspondence to: J. M. Aguilar, Avenida de Córdoba s/n, 28041 Madrid, Spain. Tel: +34 917 390 8508; Fax: +34 917 390 8772; E-mail: [email protected]
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Abstract

Aortic arch coarctation with post-coarctation aneurysm is rare in infants. We present the case of an asymptomatic 3-month-old infant with severe left ventricular dysfunction in this setting. The patient underwent surgical repair, and the left ventricular ejection fraction improved to recovery the 4th post-operative month.

Keywords

Aortacoarctationaneurysm
Type
Images in Congenital Cardiac Disease
Information
Cardiology in the Young , Volume 26 , Issue 5 , June 2016 , pp. 971 - 972
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Copyright
© Cambridge University Press 2016 

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References

1. Ozyuksel, A, Canturk, E, Dindar, A, et al. Saccular aneurysm formation of the descending aorta associated with aortic coarctation in an infant. Rev Bras Cir Cardiovasc 2014; 29: 642–644.Google ScholarPubMed
2. Bayer, ML, Frommelt, PC, Blei, F, et al. Congenital cardiac, aortic arch, and vascular bed anomalies in PHACE syndrome (from the International PHACE Syndrome Registry). Am J Cardiol 2013; 112: 1948–1952.CrossRefGoogle ScholarPubMed