首页> 外文期刊>Open Access Library Journal >Adult ALCAPA Syndrome-Anomalous Origin of Left Coronary Artery from Pulmonary Artery: A Rare Coronary Artery Anomaly Diagnosed by 256-Slice Computed Tomography
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Adult ALCAPA Syndrome-Anomalous Origin of Left Coronary Artery from Pulmonary Artery: A Rare Coronary Artery Anomaly Diagnosed by 256-Slice Computed Tomography

机译:肺动脉左冠状动脉成年ALCAPA综合征的异常起源:256片计算机断层扫描诊断的罕见冠状动脉异常。

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摘要

We are presenting a rare case of anomalous origin of left coronary artery from the pulmonary artery (ALCAPA) in an adult patient. The patient underwent coronary CT angiography for exertional dyspnoea, suspected as coronary artery disease; however there were no atherosclerotic plaques. There was anomalous origin of left coronary artery from pulmonary artery. Conventional catheter angiography confirmed the origin of left coronary artery from pulmonary artery, which was retrogradely filling through right coronary artery.
机译:我们介绍了在成年患者中罕见的左冠状动脉异常起源于肺动脉(ALCAPA)的情况。该患者因劳累性呼吸困难而进行了冠状动脉CT血管造影,怀疑是冠心病。但是,没有动脉粥样硬化斑块。左冠状动脉起源于肺动脉。传统的导管血管造影术证实左冠状动脉起源于肺动脉,并通过右冠状动脉逆行充盈。

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