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双侧先天性冠状动脉-肺动脉瘘:两例罕见病例报告。

Bilateral congenital coronary artery--pulmonary artery fistulae: report of two unusual cases.

作者信息

Gupte S S, Ryan G F, Easley R M

出版信息

Angiology. 1979 Apr;30(4):276-80. doi: 10.1177/000331977903000408.

Abstract

Congenital coronary arteriovenous fistulae involving both coronary arteries are rare. Those terminating in a right heart chamber or the pulmonary artery usually mimic a patent ductus arteriosus because of the presence of a continuous murmur. Since the vascular resistance is much lower in the pulmonary circuit than in myocardial capillaries, a large percentage of coronary blood flow may be directed through the fistula. Such a "steal" can cause myocardial ischemia distal to the origin of the fistula. Angina has been reported to occur. About 20% of coronary A-V fistulae are associated with other congenital cardiac anomalies.

摘要

累及双侧冠状动脉的先天性冠状动脉动静脉瘘很罕见。那些终止于右心腔或肺动脉的瘘通常会因存在连续性杂音而酷似动脉导管未闭。由于肺循环中的血管阻力远低于心肌毛细血管中的血管阻力,很大一部分冠状动脉血流可能会通过瘘管分流。这种“窃血”可导致瘘管起源部位远端的心肌缺血。据报道可出现心绞痛。约20%的冠状动脉动静脉瘘与其他先天性心脏异常有关。

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