Hostname: page-component-6bf8c574d5-9f2xs Total loading time: 0 Render date: 2025-03-09T13:22:42.375Z Has data issue: false hasContentIssue false
  • English
  • Français

A case of isolated right subclavian artery and right patent ductus arteriosus successfully treated with catheter intervention in early infancy

Published online by Cambridge University Press:  05 March 2025

Makoto Yoshida Open the ORCID record for Makoto Yoshida [Opens in a new window] ,
Tao Fujioka  and
Akio Inage
Makoto Yoshida*
Affiliation:
Department of Pediatrics, Japanese Red Cross Medical Center, Tokyo, Japan
Tao Fujioka
Affiliation:
Department of Pediatrics, Japanese Red Cross Medical Center, Tokyo, Japan
Akio Inage
Affiliation:
Department of Pediatrics, Japanese Red Cross Medical Center, Tokyo, Japan
*
Corresponding author: Makoto Yoshida; Email: [email protected]
Get access Rights & Permissions [Opens in a new window]

Abstract

In isolated subclavian artery, abnormal aortic arch development causes a loss of continuity with the aorta. Patent ductus arteriosus is a known cause of congestive heart failure. Herein, we present a rare case of congestive heart failure caused by isolated right subclavian artery and right patent ductus arteriosus associated with left-sided aortic arch treated by early closure.

Keywords

Isolated subclavian arteryright ductus arteriosuspercutaneous embolisationatrial septal defectheart failure
Type
Brief Report
Information
Cardiology in the Young , First View , pp. 1 - 3
Check for updates
Copyright
© The Author(s), 2025. 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

Alhuzaimi, AN, Aldawsari, KA, AlAhmadi, M. Isolated left subclavian artery with right aortic arch: case report and literature review of 50 cases. Gen Thorac Cardiovasc Surg 2021; 69: 885–889.CrossRefGoogle ScholarPubMed
Nath, PH, Castaneda-Zuniga, W, Zollikofer, C, et al. Isolation of a subclavian artery. AJR Am J Roentgenol 1981; 137: 683–688.CrossRefGoogle ScholarPubMed
Sen, S, Mohanty, S, Kulkarni, S, Rao, SG. Isolated subclavian artery: a rare entity revisited. World J Pediatr Congenit Heart Surg 2016; 7: 744–749.CrossRefGoogle ScholarPubMed
Edwards, JE. Malformations of the aortic arch system manifested as vascular rings. Lab Invest 1953; 2: 56–75.Google ScholarPubMed
Jones, TK, Garabedian, H, Grifka, RG. Right aortic arch with isolation of the left subclavian artery, moderate patent ductus arteriosus, and subclavian steal syndrome: a rare aortic arch anomaly treated with the Gianturco-grifka vascular occlusion device. Catheter Cardiovasc Interv 1999; 47: 320–322.3.0.CO;2-V>CrossRefGoogle ScholarPubMed
Koneti, NR, Qureshi, SA, Sivakumar, K. Catheter interventions for “double steal” from isolation of the subclavian artery associated with patent arterial duct. Cardiol Young 2014; 24: 95–98.CrossRefGoogle ScholarPubMed
Arunamata, A, Perry, SB, Kipps, AK, Vasanawala, SS, Axelrod, DM. Isolation of the right subclavian artery in a patient with d-transposition of the great arteries. Ann Pediatr Cardiol 2015; 8: 161–163.CrossRefGoogle Scholar
Supplementary material: File

Yoshida et al. supplementary material

Yoshida et al. supplementary material
Download Yoshida et al. supplementary material(File)
File 26.1 MB