Anomalous Left Coronary Artery From The Pulmonary Artery (ALCAPA) as a Cause of Heart Failure

被引:5
|
作者
Sadoma, Daniel [1 ]
Valente, Christopher [1 ]
Sigal, Adam [1 ]
机构
[1] Reading Hosp, Dept Emergency Med, W Reading, PA 19611 USA
来源
关键词
Bland White Garland Syndrome; Heart Failure; Pediatrics; Ultrasonography; INFANTS;
D O I
10.12659/AJCR.917655
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Rare disease Background: Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare anomaly. When present it can result in failure to thrive and congestive heart failure. Case Report: We present the case of a 6-month old female whose presentation was one of failure to thrive. Point of care ultrasound and electrocardiogram (ECG) were used to diagnose heart failure with consideration of ALCAPA. These tools helped to expedite transfer to a tertiary care center for definitive therapy. Conclusions: Although a rare anomaly, ALCAPA induced heart failure can be quickly identified on bedside ultrasound. Together with ECG findings, the Emergency Physician can expedite the diagnosis and proper disposition.
引用
收藏
页码:1797 / 1800
页数:4
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