先天性左主干冠状动脉闭锁

IF 1.4 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS

Egyptian Heart Journal Pub Date : 2018-12-01 DOI:10.1016/j.ehj.2018.10.005

Sedigheh Saedi, Hamid Reza Pouraliakbar, Homa Ghaderian, Tahereh Saedi

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引用次数: 6

摘要

先天性左主干冠状动脉闭锁是一种非常罕见的冠状动脉异常，如果不及时治疗，临床结果很差。患者诊断后需行冠状动脉搭桥术矫正。在这里，我们报告一例先天性左主干闭锁在一个36岁的妇女谁有以前的心脏手术与这种异常未被发现。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Congenital atresia of left main coronary artery

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Congenital atresia of left main coronary artery

Congenital atresia of the left main coronary artery is a very rare form of coronary anomalies with poor clinical outcomes if left untreated. Patients require surgical correction by coronary bypass grafting after diagnosis. Here we report a case of congenital left main atresia in a 36 years old woman who had previous heart surgery with this anomaly having gone undetected.

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来源期刊

Egyptian Heart Journal CARDIAC & CARDIOVASCULAR SYSTEMS-

CiteScore

2.10

自引率

0.00%

发文量

审稿时长

9 weeks

期刊介绍： The Egyptian Heart Journal is the official journal of the Egyptian Society of Cardiology. It is an international journal that publishes peer-reviewed articles on all aspects of cardiovascular disease, including original clinical studies and translational investigations. The journal publishes research, review articles, case reports and commentary articles, as well as editorials interpreting and commenting on the research presented. In addition, it provides a forum for the exchange of information on all aspects of cardiovascular medicine, including educational issues.