The anomalous origin of the left coronary artery from the pulmonary artery.
نویسنده
چکیده
The anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare malformation that represents less than 0.5% of the congenital heart diseases. The common clinical feature is congestive heart failure. The treatment is strictly a surgical repair. The authors report the first 3 cases of ALCAPA diagnosed in Senegal in infants under the age of 1 year old. Two were successfully treated by surgical repair; the 3 rd child is still waiting for surgical repair to be performed abroad.
منابع مشابه
Different Presentation of Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery in Adults: Case Reports
Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital cardiac malformation. We report three cases of ALCAPA who survived to adulthood. The first case was a 51-year-old woman who complained of typical chest pain that was diagnosed with ALCAPA using cardiac catheterization and coronary computed tomographic angiography (CTA). The second case was a 30-...
متن کاملThe Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA): a Case Series and Brief Review
Background Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital cardiovascular defect that occurs in approximately 1/300 000 live births or 0.5% of children with congenital heart disease. There are two types of ALCAPA syndrome: the infant type and the adult type. The most infants experience myocardial infarction and congestive heart failure, and approximately 9...
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متن کاملگزارش یک مورد بیماری ایسکمیک شدید قلبی در شیرخوار سه ماهه ناشی از منشاء گیری نابجای شریان کرونری چپ از تنه شریان ریوی، ارجاعی به سالن تشریح پزشکی قانونی تبریز
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ورودعنوان ژورنال:
- British heart journal
دوره 21 2 شماره
صفحات -
تاریخ انتشار 1959