晚期成人左冠状动脉异常来源肺动脉表现为心力衰竭，行取内修复术1例

IF 0.2 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS

Research in Cardiovascular Medicine Pub Date : 2023-01-01 DOI:10.4103/rcm.rcm_38_22

Soheila Salari, Zahra Khajali, Yaser Toloueitabar, Mahnaz Farajollahi, Atefe Shafiee, Sahar Molseghi

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引用次数: 0

摘要

左冠状动脉(LCA)起源于肺动脉(PA)异常是一种非常罕见的先天性异常，可能是致命的。这种冠状动脉异常的成人类型可以从无症状到心源性猝死不等。在这项研究中，我们报告了一位35岁的女性，从PA诊断为LCA，由于继发于这种异常的心肌缺血后收缩功能障碍而出现劳力呼吸困难。她接受了成功的竹内修复术，没有任何并发症。

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Late adult anomalous origin of the left coronary artery from the pulmonary artery presentation by heart failure, underwent takeuchi repair – A case report

The anomalous origin of the left coronary artery (LCA) from the pulmonary artery (PA) is a very uncommon congenital anomalous that can be fatal. The adult type of this coronary abnormality can be the presence of varied from asymptomatic to sudden cardiac death. In this study, we present a 35-year-old female with a diagnosis of LCA from the PA that present with exertional dyspnea due to systolic dysfunction after myocardial ischemia secondary to this anomaly. She underwent successful Takeuchi repair without any complications.

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来源期刊

Research in Cardiovascular Medicine CARDIAC & CARDIOVASCULAR SYSTEMS-

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0.00%

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审稿时长

17 weeks