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01-08-2019 | Ventricular Septal Defect | Anatomic Variations

Coexistence an aberrant right subclavian artery with other congenital anomalies: case report and review of the literature

Authors: Alexander Gennadievich Mrochek, Sergey Lvovich Kabak, Iryna Kazimirovna Haidzel, Yuliya Michailovna Melnichenko, Tamara Ivanovna Kalenchic

Published in: Surgical and Radiologic Anatomy | Issue 8/2019

Abstract

Aberrant right subclavian artery is the most common aortic arch anomaly that frequently occurs in coexistence with other congenital cardiovascular anomalies. A 32-year-old male patient was hospitalized with ventricular septal defect, chronic heart failure NYHA class III, pulmonary arterial hypertension. Contrast-enhanced multislice computed tomography revealed membranous ventricular septal defect, persistent left superior vena cava, bicuspid aortic valve and aberrant right subclavian artery. Aberrant right subclavian artery was clinically silent and discovered accidentally. The patient underwent heart–lung transplantation due to pronounced, irreversible pulmonary hypertension. This article reports a rare coexistence of aberrant right subclavian artery with other congenital anomalies of the heart and great vessels in living men.

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Title: Coexistence an aberrant right subclavian artery with other congenital anomalies: case report and review of the literature
Authors: Alexander Gennadievich Mrochek
Sergey Lvovich Kabak
Iryna Kazimirovna Haidzel
Yuliya Michailovna Melnichenko
Tamara Ivanovna Kalenchic
Publication date: 01-08-2019
Publisher: Springer Paris
Keywords: Ventricular Septal Defect
Hypertension
Ventricular Septal Defect
Dysphagia
Dysphagia
Arterial Hypertension
Arterial Hypertension
Dysphagia
Published in: Surgical and Radiologic Anatomy / Issue 8/2019
Print ISSN: 0930-1038
Electronic ISSN: 1279-8517
DOI: https://doi.org/10.1007/s00276-019-02206-x

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Coexistence an aberrant right subclavian artery with other congenital anomalies: case report and review of the literature

Abstract

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Abstract

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