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Revista Cubana de Cardiología y Cirugía Cardiovascular

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2022, Number 1

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Rev Cubana Cardiol Cir Cardiovasc 2022; 28 (1)

Unsuspected anomalous left coronary origin from main pulmonary artery in a young adult

Martínez GA, Marcos GY, Zorio VBY, Pérez BA, Bencomo RL, Hechavarría PS
Full text How to cite this article

Language: Spanish
References: 17
Page: 1-5
PDF size: 337.07 Kb.


Key words:

anomaly of the coronary vessels, anomalous left coronary artery, Bland White Garland syndrome, computed tomography angiography.

ABSTRACT

Anomalous left coronary origin from main pulmonary artery is a rare congenital defect. Generally detected in infants, it is less common in adults, and its prognosis varies considerably if the diagnosis and surgical treatment are performed in a timely manner. Non-invasive imaging techniques have made it possible to improve its identification. This presentation is intended to broaden the knowledge of the peculiarities of anomalous left coronary artery from the pulmonary artery syndrome (ALCAPA) in adults. The case of a young patient with exertional dyspnea is reported here and, with no clinical suspicion, marked coronary dilations derived from the anomalous origin of the left coronary artery are evident. Tomography angiography has become the diagnostic modality of choice for evaluation coronary anomalies, by allowing their identification, the accompanying alterations and other associated anomalies. Every report of ALCAPA syndrome allows us to provide data that make it possible to expand knowledge about this unusual but lethal coronary anomaly.


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Rev Cubana Cardiol Cir Cardiovasc. 2022;28