与右冠状巨动脉瘤相关的左冠状动脉异常起源于肺动脉。

IF 1.1 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS World Journal for Pediatric and Congenital Heart Surgery Pub Date : 2023-03-01 DOI:10.1177/21501351221135767
Martin Antelo, Diego Freire, Alvaro Dendi, Gabriel Parma, Nicolas Fernandez, Dante Picarelli
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引用次数: 0

摘要

左冠状动脉起源地异常(ALCAPA)是一种罕见的先天性畸形,通常在婴儿时期因心肌缺血和心力衰竭而诊断出来,需要紧急手术治疗。不太常见的是,它可以在成年前没有症状。冠状动脉瘤也是一种罕见的解剖异常,具有急性或慢性心绞痛的症状,甚至完全没有症状。我们提出一个不寻常的病例ALCAPA,与一个巨大的动脉瘤的右冠状动脉。会议介绍:美国胸外科协会第102届年会,美国马萨诸塞州波士顿,2022年5月16日。
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Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery Associated with Right Coronary Giant Aneurysm.

Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital malformation, usually diagnosed in the infant period due to myocardial ischemia and heart failure, with the need for emergency surgery. Less commonly, it can be asymptomatic until adulthood. Coronary artery aneurysms are also rare anatomical anomalies with symptoms of acute or chronic angina or even remain completely asymptomatic. We present an unusual case of ALCAPA, associated with a giant aneurysm of the right coronary artery. Meeting presentation: American Association for Thoracic Surgery 102nd annual meeting, Boston MA, USA, May 16, 2022.

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CiteScore
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11.10%
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128
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