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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]
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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
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Copyright
© The Author(s), 2022. Published by Cambridge University Press

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