Anomalous Origin of the Right Subclavian Artery from the Right Pulmonary Artery in a Patient with d-Transposition of the Great Arteries: Diagnosis and Surgical Treatment

Anomalous origin of the right subclavian artery (AORSA) from the right pulmonary artery is a rare congenital anomaly usually diagnosed by computed tomography, magnetic resonance imaging, or angiography. We present a very rare case of diagnosis and surgical correction of AORSA coexisting with d-transposition of the great arteries in a newborn's first hours of life. Due to the critical local hospital and patient conditions, additional cross-sectional imaging was not feasible. The diagnosis was suspected by clinical signs, confirmed by transthoracic echocardiogram, and the patient was urgently taken to the operating room. We discuss clinical and echocardiographic signs of this child with d-transposition of the great arteries and AORSA from the right pulmonary artery.

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Publication Details

Journal
World Journal for Pediatric and Congenital Heart Surgery
Published
2024-11-03
DOI
https://doi.org/10.1177/21501351241286450
Primary Topic
Congenital Heart Disease Studies
Type
article
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article

Anomalous Origin of the Right Subclavian Artery from the Right Pulmonary Artery in a Patient with d-Transposition of the Great Arteries: Diagnosis and Surgical Treatment

Dmytro Kozhokar, Roman Sekelyk, Andrii Kurkevych, Danylo Shypov et al.
World Journal for Pediatric and Congenital Heart Surgery
Congenital Heart Disease Studies
article

Anomalous Origin of the Right Subclavian Artery from the Right Pulmonary Artery in a Patient with d-Transposition of the Great Arteries: Diagnosis and Surgical Treatment

Dmytro Kozhokar, Roman Sekelyk, Andrii Kurkevych, Danylo Shypov, Illya Yemets, I. Yusifli, Maksym Delikatnyi
article en

Abstract

Anomalous origin of the right subclavian artery (AORSA) from the right pulmonary artery is a rare congenital anomaly usually diagnosed by computed tomography, magnetic resonance imaging, or angiography. We present a very rare case of diagnosis and surgical correction of AORSA coexisting with d-transposition of the great arteries in a newborn's first hours of life. Due to the critical local hospital and patient conditions, additional cross-sectional imaging was not feasible. The diagnosis was suspected by clinical signs, confirmed by transthoracic echocardiogram, and the patient was urgently taken to the operating room. We discuss clinical and echocardiographic signs of this child with d-transposition of the great arteries and AORSA from the right pulmonary artery.

World Journal for Pediatric and Congenital Heart SurgeryVol. 16(1)
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Openalex Percentile: Top 71%
Congenital Heart Disease Studies
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