Hostname: page-component-586b7cd67f-rdxmf Total loading time: 0 Render date: 2024-11-26T11:16:47.060Z Has data issue: false hasContentIssue false

A rare case of congenital heart disease: anomalous origin of coronary artery from innominate artery with coronary fistula and truncus arteriosus

Published online by Cambridge University Press:  18 February 2021

Wenlei Li
Affiliation:
Department of Cardiac Surgery, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, China
Jianbin Li
Affiliation:
Department of Cardiac Surgery, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, China
Xinxin Chen*
Affiliation:
Department of Cardiac Surgery, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, China
*
Author for correspondence: Xinxin Chen, Department of Cardiac Surgery, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, 9# Jinsui Road, Guangzhou510623, China. Tel: +862038076180. E-mail: [email protected]

Abstract

Anomalous origin of a single coronary artery arising from the innominate artery associated with coronary artery fistula and truncus arteriosus is extremely rare. We found this anomaly in a 16-month-old infant-girl who received Rastelli procedure during the operation. The three defects described above are rarely found together; indeed, such a case as ours may be the first reported in the literature.

Type
Brief Report
Copyright
© The Author(s), 2021. Published by Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Russell, HM, Pasquali, SK, Jacobs, JP et al. Outcomes of repair of common arterial trunk with truncal valve surgery: a review of the society of thoracic surgeons congenital heart surgery database. Ann Thorac Surg 2012; 93: 164169; discussion 169.10.1016/j.athoracsur.2011.04.121CrossRefGoogle Scholar
Marcelletti, C, McGoon, DC, Mair, DD. The natural history of truncus arteriosus. Circulation 1976; 54: 108111.CrossRefGoogle ScholarPubMed
Lenox, CC, Debich, DE, Zuberbuhler, JR. The role of coronary artery abnormalities in the prognosis of truncus arteriosus. J Thorac Cardiovasc Surg 1992; 104: 17281742.10.1016/S0022-5223(19)33907-8CrossRefGoogle ScholarPubMed
Naimo, PS, Fricke, TA, Yong, MS et al. Outcomes of Truncus Arteriosus Repair in Children: 35 Years of Experience From a Single Institution. Semin Thorac Cardiovasc Surg 2016; 28: 500511.10.1053/j.semtcvs.2015.08.009CrossRefGoogle ScholarPubMed
Bonilla-Ramirez, C, Ibarra, C, Binsalamah, ZM, et al. Coronary Artery Anomalies Are Associated with Increased Mortality After Truncus Arteriosus Repair. Ann Thorac Surg 2020.Google ScholarPubMed
Liu, F, Huang, G, Zhang, J. Anomalous origin of a coronary artery from the right branchiocephalic trunk associated with complex congenital heart disease. Pediatr Cardiol 2010; 31: 163165.CrossRefGoogle ScholarPubMed
Jung, JC, Kwak, JG, Kim, ER, et al. Reoperation for coronary artery stenosis after arterial switch operation. Interact Cardiovasc Thorac Surg 2018; 27: 169176.10.1093/icvts/ivy077CrossRefGoogle ScholarPubMed