Common arterial trunk with pulmonary atresia

We report two congenitally malformed hearts found at autopsy to have common arterial trunk and pulmonary atresia. Both exhibited usual atrial arrangement, along with concordant atrioventricular connections. In one case, the common arterial trunk arose predominantly from the right ventricle, while the other had a balanced commitment. In both, the atretic pulmonary trunk arose from the left posterolateral aspect of the common trunk. Confluent right and left pulmonary arteries, which were hypoplastic but patent, were present. On the inner aspect of the common trunk, there was a dimple immediately adjacent to the atretic segment of the pulmonary component identified externally. In one case, the fibrous pulmonary component had been accidentally cut during dissection. A solitary coronary artery was identified in both cases.

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Publication Details

Journal
Cardiology in the Young
Published
2024-11-01
DOI
https://doi.org/10.1017/s1047951124035972
Primary Topic
Congenital Heart Disease Studies
Type
article
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article

Common arterial trunk with pulmonary atresia

Rohit S. Loomba, Diane E. Spicer, Robert H. Anderson, Briana Kittredge
Cardiology in the Young
Congenital Heart Disease Studies
article

Common arterial trunk with pulmonary atresia

Rohit S. Loomba, Diane E. Spicer, Robert H. Anderson, Briana Kittredge
article en

Abstract

We report two congenitally malformed hearts found at autopsy to have common arterial trunk and pulmonary atresia. Both exhibited usual atrial arrangement, along with concordant atrioventricular connections. In one case, the common arterial trunk arose predominantly from the right ventricle, while the other had a balanced commitment. In both, the atretic pulmonary trunk arose from the left posterolateral aspect of the common trunk. Confluent right and left pulmonary arteries, which were hypoplastic but patent, were present. On the inner aspect of the common trunk, there was a dimple immediately adjacent to the atretic segment of the pulmonary component identified externally. In one case, the fibrous pulmonary component had been accidentally cut during dissection. A solitary coronary artery was identified in both cases.

Cardiology in the YoungVol. 34(11)
Northwestern University (US), Lurie Children's Hospital (US), Johns Hopkins University (US), Johns Hopkins All Children's Hospital (US), Phoenix Children's Hospital (US), Newcastle University (GB)
Openalex Percentile: Top 69%
Congenital Heart Disease Studies
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