Repair of an anomalous origin of the left pulmonary artery from the ascending aorta.
نویسندگان
چکیده
Anomalous origin of a left pulmonary artery from the ascending aorta is a very uncommon congenital cardiac malformation. Different surgical techniques have been employed. The direct implantation has been the strategy of choice. However, postoperative restenosis across the anastomotic site is frequently observed. We present a case in which a flap of the left pulmonary artery was used downward along the main pulmonary artery after excision, in a transverse diamond-shape, of the fusion of the media wall between them. This technique is feasible and effective to achieve a noncircular anastomosis without any prosthetic material.
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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OBJECTIVE To emphasize the diagnostic possibility of the anomalous origin of one pulmonary artery from the ascending aorta in infants with clinically refractory heart failure and no intracardiac structural defect. METHODS Retrospective study of 4 infants with refractory heart failure undergoing 2-dimensional echocardiographic study with subcostal, suprasternal, and parasternal views, and hemo...
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The anomalous origin of one pulmonary artery branch from the aorta (AOPA) is rare. We report our single-institution surgical experience with this condition. Between January 1994 and February 2011, 17 patients (age: 1 month-25 years) with AOPA underwent surgery at our institute. Thirteen patients had an anomalous origin of the right pulmonary artery (RPA) while four had an anomalous origin of th...
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عنوان ژورنال:
- The Annals of thoracic surgery
دوره 96 5 شماره
صفحات -
تاریخ انتشار 2013