Hostname: page-component-7479d7b7d-wxhwt Total loading time: 0 Render date: 2024-07-11T11:25:27.956Z Has data issue: false hasContentIssue false
  • English
  • Français

Isolated right subclavian artery in a left aortic arch with ventricular septal defect

Published online by Cambridge University Press:  16 December 2020

Ayed A. Shati Open the ORCID record for Ayed A. Shati [Opens in a new window]
Ayed A. Shati*
Affiliation:
Department of Child Health, College of Medicine, King Khalid University, Abha, Saudi Arabia
*
Address for correspondence: Ayed A. Shati, Department of Child Health, College of Medicine, King Khalid University, P.O. Box 641, Abha, Saudi Arabia. Tel: +966555752063. E-mail: shatiayed@gmail.com
Get access Rights & Permissions [Opens in a new window]

Abstract

Isolated origin of the subclavian artery is a congenital anomaly of the aortic arch in which one subclavian artery is attached to the ipsilateral pulmonary artery through ligamentous arteriosus. An isolated right subclavian artery with the left-sided aortic arch is an extremely rare condition. We report on an asymptomatic 2-year-old-girl, who was referred because of an incidental cardiac a murmur. She was diagnosed by echocardiography to have an isolated right subclavian artery connected to the right pulmonary artery in a left aortic arch with a ventricular septal defect. MRI confirmed the findings.

Keywords

Isolated right subclavian arteryleft aortic archventricular septal defect
Type
Brief Report
Information
Cardiology in the Young , Volume 31 , Issue 4 , April 2021 , pp. 669 - 670
Check for updates
Copyright
© The Author(s), 2020. 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

Stewart, JR, Kincaid, OW, Edwards, JE. An Atlas of Vascular Rings and Related Malformations of the Aortic Arch System. Charles C Thomas, Publisher, Springfield, Illinois, 1964.Google Scholar
Stewart, JR, Kincaid, OW, Titus, JL. Right aortic arch: plain film diagnosis and significance. Am J Roentgenol 1966; 97: 377–389.CrossRefGoogle ScholarPubMed
Kutsche, LM, Van Mierop, LHS. Anomalous origin of a pulmonary artery from the ascending aorta: associated anomalies and pathogenesis. Am J Cardiol 1988; 61: 850–856.CrossRefGoogle ScholarPubMed
Penkoske, PA, Castaneda, AR, Fyler, DC, Van Praagh, R. Origin of pulmonary artery branch from the ascending aorta. Primary surgical repair in infancy. J Thorac Cardiovasc Surg 1983; 85: 537–545.CrossRefGoogle ScholarPubMed
Johnson, MC, Watson, MS, Strauss, AW, Spray, TL. Anomalous origin of the right pulmonary artery from the aorta and CATCH 22 syndrome. Ann Thorac Surg 1995; 60: 681–683.CrossRefGoogle ScholarPubMed
Edwards, JE. Anomalies of the aortic arch system. Birth Defects 1977; 13: 47–63.Google ScholarPubMed
Mittal, PK, Agarwal, SK, Ghosh, PK. Isolated anomalous origin of the left pulmonary artery from the ascending aorta in an adult. J Thorac Cardiovasc Surg 1993; 106: 1220–1223.CrossRefGoogle ScholarPubMed
Duncan, WJ, Freedom, RM, Olley, PM, Rowe, RD. Two-dimensional echocardiographic identification of hemitruncus: anomalous origin of one pulmonary artery from ascending aorta with the other pulmonary artery arising normally from the right ventricle. Am Heart J 1981; 102: 892–896.CrossRefGoogle ScholarPubMed
Katayama, H, Shimizu, T, Tanaka, Y, Narabayashi, I, Tamai, H. Three-dimensional magnetic resonance angiography of vascular lesions in children. Heart Vessels 2000; 15: 1–6.CrossRefGoogle ScholarPubMed