An experience with off pump technique for repair of anomalous left coronary artery from pulmonary artery (ALCAPA)
نویسندگان
چکیده
منابع مشابه
Anomalous origin of left coronary artery from pulmonary artery (ALCAPA).
Anomalous origin of the left coronary artery from the pulmonary artery also recognized as Bland White Garland syndrome is a very rare congenital condition. A two-months old baby boy presented with dyspnoea for two weeks and a pansystolic murmur on auscultation. The base line investigations showed cardiomegaly and bilateral basal haze on X-ray chest. ECG showed ST elevation in leads l and AVl an...
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...
متن کاملThe caveats in the diagnosis of anomalous origin of left coronary artery from pulmonary artery (ALCAPA)
Anomalous origin of left coronary artery from pulmonary artery (ALCAPA) is an infrequent, well described, but important anomaly of the coronary origin. Early diagnosis and prompt surgical treatment of the disease can be life saving. However, there are several potential sources of error in the seemingly simple stereotype diagnostic pattern. We report a case of ALCAPA and allude to some of the ca...
متن کاملAnomalous Origin of Left Main Coronary Artery from Pulmonary Artery (alcapa)
Anomalous origin of left main coronary artery from pulmonary artery (ALCAPA) is a very rare congenital anomaly, reported in less than 0.5% of all the congenital heart diseases. Left untreated, majority of the patients die in infancy of myocardial ischemia. We report a case with this anomaly, presented in early infancy with progressive dyspnoea, feeding difficulty and cardiomagaly on X-ray. The ...
متن کاملAnomalous Origin of Left Coronary Artery from Pulmonary Artery [alcapa] –a Case Report
ALCAPA a rare congenital coronary anomaly, which usually manifests as an isolated defect, and can develop when there is an embryological failure of normal communication to the left coronary bud in the aorta, with an abnormal connection to the pulmonary bud instead. If left untreated, up to 90% of pediatric patients with this syndrome die within the 1st year of life. To survive beyond infancy, p...
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ژورنال
عنوان ژورنال: Indian Heart Journal
سال: 2016
ISSN: 0019-4832
DOI: 10.1016/j.ihj.2016.02.002