Hostname: page-component-586b7cd67f-t8hqh Total loading time: 0 Render date: 2024-11-22T16:33:21.137Z Has data issue: false hasContentIssue false
  • English
  • Français

Hybrid management of dysphagia lusoria in a boy with Duchenne’s muscular dystrophy

Published online by Cambridge University Press:  13 April 2022

Peter Chiu Open the ORCID record for Peter Chiu [Opens in a new window] ,
Stanton Perry ,
Daniel Bernstein  and
Katsuhide Maeda
Peter Chiu
Affiliation:
Department of Cardiothoracic Surgery, Stanford University School of Medicine, Stanford, CA, USA
Stanton Perry
Affiliation:
Division of Pediatric Cardiology, Stanford University School of Medicine, Stanford, CA, USA
Daniel Bernstein
Affiliation:
Division of Pediatric Cardiology, Stanford University School of Medicine, Stanford, CA, USA
Katsuhide Maeda*
Affiliation:
Division of Pediatric Cardiac Surgery, Stanford University School of Medicine, Stanford, CA, USA
*
Author for correspondence: K. Maeda, MD, 3401 Civic Center Blvd, Philadelphia, PA 19104, USA. Tel: (650) 724-2925; Fax: (650) 725-0707. E-mail: [email protected]
Get access Rights & Permissions [Opens in a new window]

Abstract

We present a case of dysphagia lusoria in a wheelchair-bound 9-year-old boy with Duchenne’s muscular dystrophy. Due to the patient’s limited mobility and restrictive ventilatory defect, the patient was too high risk for open repair, and hybrid revascularisation with carotid-to-subclavian bypass and endovascular occlusion of the proximal right subclavian was undertaken. The patient has been followed up for 18 months with no residual symptoms.

Keywords

Endovasculardysphagia lusoriaaberrant subclavian
Type
Brief Report
Information
Cardiology in the Young , Volume 32 , Issue 11 , November 2022 , pp. 1842 - 1844
Check for updates
Copyright
© The Author(s), 2022. 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

Austin, EH, Wolfe, WG. Aneurysm of aberrant subclavian artery with a review of the literature. J Vasc Surg 1985; 2: 571–577.CrossRefGoogle ScholarPubMed
Verzini, F, Isernia, G, Simonte, G, et al. Results of aberrant right subclavian artery aneurysm repair. J Vasc Surg 2015; 62: 343–350.CrossRefGoogle ScholarPubMed
van Bogerijen, GH, Patel, HJ, Eliason, JL, et al. Evolution in the management of aberrant subclavian arteries and related Kommerell diverticulum. Ann Thorac Surg 2015; 100: 47–53.CrossRefGoogle ScholarPubMed
Bloom, JP, Attia, RQ, Sundt, TM, et al. Outcomes of open and endovascular repair of Kommerell diverticulum. Eur J Cardiothorac Surg 2021; 60: 305–311.CrossRefGoogle ScholarPubMed
Saran, N, Dearani, J, Said, S, et al. Vascular rings in adults: outcome of surgical management. Ann Thorac Surg 2019; 108: 1217–1227.CrossRefGoogle ScholarPubMed
Soo Hoo, AJ, Rokkas, CK, Rossi, PJ. Migration of endovascular plug in hybrid repair of dysphagia lusoria. J Vasc Surg Cases Innov Tech 2018; 4: 140–143.CrossRefGoogle ScholarPubMed
Jalaie, H, Grommes, J, Sailer, A, et al. Treatment of symptomatic aberrant subclavian arteries. Eur J Vasc Endovasc Surg 2014; 48: 521–526.CrossRefGoogle ScholarPubMed