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Scimitar syndrome and anomalous origin of the circumflex artery from the main pulmonary artery in infancy: a case report

Published online by Cambridge University Press:  05 March 2013

Luciana D. F. Marcondes*
Affiliation:
Department of Paediatrics, Royal Brompton and Harefield Trust, London, United Kingdom
Olivier Ghez
Affiliation:
Department of Cardiac Surgery, Royal Brompton and Harefield Trust, London, United Kingdom
Alan G. Magee
Affiliation:
Department of Paediatrics, Royal Brompton and Harefield Trust, London, United Kingdom
*
Correspondence to: Luciana Marcondes, MD, Paediatric Cardiology fellow, Department of Paediatrics, Royal Brompton and Harefield Trust, Sydney Street, London SW3 6NP, United Kingdom. Tel: +44 (0)20 7352 8731; Fax: +44 20 7351 8206; E-mail: lucianamarcondes@outlook.com

Abstract

We present a neonate with an antenatal diagnosis of Scimitar syndrome and aortic arch hypoplasia. After delivery, computerised tomography scan additionally revealed an anomalous origin of the circumflex coronary artery from the main pulmonary artery. The management of this rare combination is discussed.

Type
Brief Reports
Copyright
Copyright © Cambridge University Press 2013 

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References

1. Gao, Y, Burrows, PE, Benson, LN, Rabinovitch, M, Freedom, RM. Scimitar syndrome in infancy. J Am Coll Cardiol 1993; 22: 873882.CrossRefGoogle ScholarPubMed
2. Vida, L, Padalino, MA, Boncuzzo, G, et al. Scimitar syndrome: a European Congenital Heart Surgeons Association (ECHSA). Circulation 2010; 122: 11591166.CrossRefGoogle ScholarPubMed
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4. Lee, TM. Anomalous origin of left circumflex artery in a scimitar syndrome. A case report. Angiology 1995; 46: 957961.CrossRefGoogle Scholar
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