3岁儿童无症状ALCAPA并保留心肌功能。

IF 1.4 4区医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS

Pediatric Cardiology Pub Date : 2025-09-08 DOI:10.1007/s00246-025-04012-2

C Leclercq, F Kaladji, J P Vallée, T Nalecz, T Sologashvili, M Beghetti, J Wacker

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引用次数: 0

摘要

摘要左冠状动脉起源于肺动脉异常是一种罕见的先天性异常。其临床病程通常在婴儿期严重，可导致左心室缺血、心源性休克和无手术干预的高死亡率。我们描述一个罕见的3岁女孩诊断为ALCAPA，显示广泛的右至左侧枝，保留左心室功能，和最小的心肌损伤。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Asymptomatic ALCAPA with Preserved Myocardial Function in a 3-Year-Old Child.

Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital anomaly. Its clinical course is typically severe in infancy, leading to left ventricular ischemia, cardiogenic shock, and high mortality without surgical intervention.We describe a rare case of a 3-year-old girl diagnosed with ALCAPA, showing extensive right-to-left collaterals, preserved left ventricular function, and minimal myocardial injury.

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来源期刊

Pediatric Cardiology 医学-小儿科

CiteScore

3.30

自引率

6.20%

发文量

258

审稿时长

12 months

期刊介绍： The editor of Pediatric Cardiology welcomes original manuscripts concerning all aspects of heart disease in infants, children, and adolescents, including embryology and anatomy, physiology and pharmacology, biochemistry, pathology, genetics, radiology, clinical aspects, investigative cardiology, electrophysiology and echocardiography, and cardiac surgery. Articles which may include original articles, review articles, letters to the editor etc., must be written in English and must be submitted solely to Pediatric Cardiology.