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Major aortopulmonary collateral arteries in association with atrioventricular septal defect with balanced ventricles and trisomy 21

Published online by Cambridge University Press:  13 May 2022

Nupur N. Makkar Open the ORCID record for Nupur N. Makkar [Opens in a new window] ,
Stephanie A. Raymundo Open the ORCID record for Stephanie A. Raymundo [Opens in a new window]  and
Roberto G. Gallotti
Nupur N. Makkar
Affiliation:
Department of Pediatrics, UCLA Mattel Children’s Hospital, Los Angeles, CA, USA
Stephanie A. Raymundo
Affiliation:
Department of Pediatric Cardiology, UCLA Mattel Children’s Hospital, Los Angeles, CA, USA
Roberto G. Gallotti*
Affiliation:
Department of Pediatric Cardiology, Seattle Children’s Hospital, Seattle, WA, USA
*
Author for correspondence: R.G. Gallotti, MD, Department of Pediatric Cardiology, Seattle Children’s Hospital, 4800 Sand Point Way NE, Seattle, WA 98105, USA. Tel: (206)987-2266. E-mail: [email protected]
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Abstract

A major aortopulmonary collateral artery is a rare and easily missed diagnosis that is usually associated with Tetralogy of Fallot or pulmonary atresia. We present two cases of major aortopulmonary collaterals associated with trisomy 21 and atrioventricular septal defect with balanced ventricles in which the diagnosis went undetected until after initial cardiac repair.

Keywords

Aortopulmonaryatrioventricularcanalcollateralarterytrisomy
Type
Brief Report
Information
Cardiology in the Young , Volume 32 , Issue 12 , December 2022 , pp. 2024 - 2026
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Copyright
© The Author(s), 2022. Published by Cambridge University Press

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References

Boshoff, D, Gewillig, M. A review of the options for treatment of major aortopulmonary collateral arteries in the setting of tetralogy of Fallot with pulmonary atresia. Cardiol Young 2006; 16: 212–220.CrossRefGoogle ScholarPubMed
Patrick, WL, Mainwaring, RD, Reinhartz, O, Punn, R, Tacy, T, Hanley, FL. Major aortopulmonary collateral arteries with anatomy other than pulmonary atresia/ventricular septal defect. Ann Thorac Surg 2017; 104: 907–916.CrossRefGoogle ScholarPubMed
Kunwar, BK, Paddalwar, S, Ghogare, M. Large isolated major aortopulmonary collateral artery causing severe pulmonary hypertension in an infant: a rare and challenging diagnosis. J Clin Diagn Res 2017; 11: 18–20.Google Scholar
Rastelli, GC, Kirklin, JW, Titus, JL. Anatomic observations on complete form of common atrioventricular canal with special reference to atrioventricular valves. Mayo Clinic Proc 1966; 41: 296–308.Google ScholarPubMed
Krishnamurthy, R, Golriz, F, Toole, BJ, Qureshi, AM, Crystal, MA. Comparison of computed tomography angiography versus cardiac catheterization for preoperative evaluation of major aortopulmonary collateral arteries in pulmonary atresia with ventricular septal defect. Ann Pediatr Cardiol 2020; 13: 117–122.Google ScholarPubMed