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Merged bilateral arterial duct and circumflex retroesophageal right aortic arch in a fetus with normal intracardiac anatomy

Part of: Cardiac Morphology

Published online by Cambridge University Press:  04 November 2019

Saïd Bichali Open the ORCID record for Saïd Bichali [Opens in a new window] ,
Romulus Cristian Grigorescu ,
Mathilde Lefebvre ,
Charlotte Oriot ,
Ferdinand Dhombres ,
Damien Bonnet  and
Lucile Houyel
Saïd Bichali*
Affiliation:
Pediatric Cardiology, Centre de Référence Malformations Cardiaques Congénitales Complexes – M3C, Necker Hospital for Sick Children, Assistance Publique des Hôpitaux de Paris, Paris, France Pediatric Cardiology, Hôpital Femme-Enfant-Adolescent, Centre Hospitalier Universitaire de Nantes, Nantes, France
Romulus Cristian Grigorescu
Affiliation:
Foetopathology, Hôpital Armand-Trousseau, Assistance Publique des Hôpitaux de Paris, Paris, France
Mathilde Lefebvre
Affiliation:
Foetopathology, Hôpital Armand-Trousseau, Assistance Publique des Hôpitaux de Paris, Paris, France
Charlotte Oriot
Affiliation:
Pediatrics, Hôpital Femme-Enfant-Adolescent, Centre Hospitalier Universitaire de Nantes, Nantes, France
Ferdinand Dhombres
Affiliation:
Obstetrics, Hôpital Armand-Trousseau, Assistance Publique des Hôpitaux de Paris, Paris, France
Damien Bonnet
Affiliation:
Pediatric Cardiology, Centre de Référence Malformations Cardiaques Congénitales Complexes – M3C, Necker Hospital for Sick Children, Assistance Publique des Hôpitaux de Paris, Paris, France Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Lucile Houyel
Affiliation:
Pediatric Cardiology, Centre de Référence Malformations Cardiaques Congénitales Complexes – M3C, Necker Hospital for Sick Children, Assistance Publique des Hôpitaux de Paris, Paris, France Université Paris Descartes, Sorbonne Paris Cité, Paris, France
*
Author for correspondence: Saïd Bichali, Hôpital Femme-Enfant-Adolescent, 38 Boulevard Jean Monnet, 44093 Nantes, 0033240083333, France. E-mail: [email protected]
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Abstract

We report the case of a fetus with anamnios sequence and VACTERL syndrome, having a circumflex right aortic arch. Two arterial ducts join anteriorly to form a common vessel that connects to the pulmonary trunk with confluent pulmonary branches. Embryologically, the dorsal right 6th aortic arch did not disappear and the aortic arch development stopped in a symmetrical state with an exceptional “Y-shaped” merged bilateral arterial duct.

Keywords

Bilateral arterial ductcircumflex aortic archright aortic archVACTERL
Type
Brief Report
Information
Cardiology in the Young , Volume 29 , Issue 12 , December 2019 , pp. 1546 - 1548
Copyright
© Cambridge University Press 2019 

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References

Li, S, Wen, H, Liang, M, et al. Congenital abnormalities of the aortic arch: revisiting the 1964 Stewart classification. Cardiovasc Pathol Off J Soc Cardiovasc Pathol 2018; 39: 38–50.CrossRefGoogle ScholarPubMed
Freedom, RM, Moes, CA, Pelech, A, et al. Bilateral ductus arteriosus (or remnant): an analysis of 27 patients. Am J Cardiol 1984; 53: 884–891.CrossRefGoogle ScholarPubMed
McLeary, MS, Frye, LL, Young, LW. Magnetic resonance imaging of a left circumflex aortic arch and aberrant right subclavian artery: the other vascular ring. Pediatr Radiol 1998; 28: 263–265.CrossRefGoogle ScholarPubMed
Robotin, MC, Bruniaux, J, Serraf, A, et al. Unusual forms of tracheobronchial compression in infants with congenital heart disease. J Thorac Cardiovasc Surg 1996; 112: 415–423.CrossRefGoogle ScholarPubMed
Hastreiter, AR, D’Cruz, IA, Cantez, T, Namin, EP, Licata, R. Right-sided aorta. I. Occurrence of right aortic arch in various types of congenital heart disease. II. Right aortic arch, right descending aorta, and associated anomalies. Br Heart J 1966; 28: 722–739.CrossRefGoogle ScholarPubMed
Knight, L, Edwards, JE. Right aortic arch. Types and associated cardiac anomalies. Circulation 1974; 50: 1047–1051.CrossRefGoogle ScholarPubMed
Felson, B, Palayew, MJ. The two types of right aortic arch. Radiology 1963; 81: 745–759.CrossRefGoogle ScholarPubMed
McElhinney, DB, Clark, BJ, Weinberg, PM, et al. Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branching. J Am Coll Cardiol 2001; 37: 2114–2119.CrossRefGoogle Scholar
Kahkouee, S, Sadr, M, Pedarzadeh, E, et al. Anomalous left brachiocephalic vein: important vascular anomaly concomitant with congenital anomalies and heart diseases. Folia Morphol 2017; 76: 51–57.CrossRefGoogle ScholarPubMed
Gupta, SK, Bamforth, SD, Anderson, RH. How frequent is the fifth arch artery? Cardiol Young 2015; 25: 628–646.CrossRefGoogle ScholarPubMed
Solomon, BD, Pineda-Alvarez, DE, Raam, MS, et al. Analysis of component findings in 79 patients diagnosed with VACTERL association. Am J Med Genet A 2010; 152A: 2236–2244.CrossRefGoogle ScholarPubMed
Cunningham, BK, Hadley, DW, Hannoush, H, et al. Analysis of cardiac anomalies in VACTERL association. Birt Defects Res A Clin Mol Teratol 2013; 97: 792–797.CrossRefGoogle ScholarPubMed
Kolesová, H, Roelink, H, Grim, M. Sonic hedgehog is required for the assembly and remodeling of branchial arch blood vessels. Dev Dyn Off Publ Am Assoc Anat 2008; 237: 1923–1934.Google ScholarPubMed