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Tricuspid atresia and common arterial trunk: a rare form of CHD

Published online by Cambridge University Press:  06 December 2022

Julia Weld*
Affiliation:
Advocate Children’s Heart Institute, Advocate Children’s Hospital, Oak Lawn, IL, USA
Brian Lee
Affiliation:
Advocate Children’s Heart Institute, Advocate Children’s Hospital, Oak Lawn, IL, USA
Rohit S. Loomba
Affiliation:
Advocate Children’s Heart Institute, Advocate Children’s Hospital, Oak Lawn, IL, USA Chicago Medical School/Rosalind Franklin School of Medicine and Science, Chicago, IL, USA
Saad Siddiqui
Affiliation:
Advocate Children’s Heart Institute, Advocate Children’s Hospital, Oak Lawn, IL, USA
Amina Jaji
Affiliation:
Advocate Children’s Heart Institute, Advocate Children’s Hospital, Oak Lawn, IL, USA
Luca Vricella
Affiliation:
Advocate Children’s Heart Institute, Advocate Children’s Hospital, Oak Lawn, IL, USA Department of Pediatric Cardiac Surgery, University of Chicago, Chicago, IL, USA
Narutoshi Hibino
Affiliation:
Advocate Children’s Heart Institute, Advocate Children’s Hospital, Oak Lawn, IL, USA Department of Pediatric Cardiac Surgery, University of Chicago, Chicago, IL, USA
Robert H. Anderson
Affiliation:
Institute of Medical Genetics, Newcastle University, London, UK
Chawki Elzein
Affiliation:
Advocate Children’s Heart Institute, Advocate Children’s Hospital, Oak Lawn, IL, USA
*
Author for correspondence: Julia Weld, Department of Pediatric Cardiology, Advocate Children’s Hospital, Oak Lawn, IL 60453, USA. Tel: 708-684-5580; Fax: 708-684-4068. E-mail: juliakweld@gmail.com

Abstract

Tricuspid atresia with common arterial trunk is a very rare association in complex CHD. This association has even more infrequently been documented concomitantly with interrupted aortic arch. We present the diagnosis and initial surgical management of an infant with a fetal diagnosis of tricuspid atresia and common arterial trunk, with additional postnatal finding of interrupted aortic arch with interruption between the left common carotid and left subclavian artery. Due to the infant’s small size, she was initially palliated with bilateral pulmonary artery bands and a ductal stent. This was followed by septation of the common arterial trunk and interrupted aortic arch repair and 4 mm right subclavian artery to main pulmonary artery shunt placement at two months of age. She was discharged home on day of life 81.

Type
Brief Report
Copyright
© The Author(s), 2022. Published by Cambridge University Press

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