Anomalous origin of the left coronary artery from the right pulmonary artery

نویسندگان

چکیده

Key Clinical Message ALCAPA should be considered in the differential diagnosis of myocarditis, and contrast‐enhanced CT or catheterization even if coronary artery abnormalities are not detected on echocardiography.

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منابع مشابه

The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA): a Case Series and Brief Review

Background Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital cardiovascular defect that occurs in approximately 1/300 000 live births or 0.5% of children with congenital heart disease. There are two types of ALCAPA syndrome: the infant type and the adult type. The most infants experience myocardial infarction and congestive heart failure, and approximately 9...

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Different Presentation of Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery in Adults: Case Reports

Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital cardiac malformation. We report three cases of ALCAPA who survived to adulthood. The first case was a 51-year-old woman who complained of typical chest pain that was diagnosed with ALCAPA using cardiac catheterization and coronary computed tomographic angiography (CTA). The second case was a 30-...

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Anomalous origin of right coronary artery from the pulmonary artery.

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Anomalous left coronary artery arising from the right pulmonary artery.

In this study, we describe a very rare case of anomalous left coronary artery arising from the right pulmonary artery in association with coarctation of the aorta. A 3-month-old boy presented with refractory congestive heart failure since 20 days after birth. The initial echocardiography suggested the diagnosis of left coronary artery-to-right pulmonary artery fistula associated with coarctatio...

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ژورنال

عنوان ژورنال: Clinical Case Reports

سال: 2023

ISSN: ['2050-0904']

DOI: https://doi.org/10.1002/ccr3.7757