Anomalous left coronary artery from the pulmonary artery (ALCAPA) – an adult who has remained asymptomatic (RCD code:I-1C.3)
نویسندگان
چکیده
منابع مشابه
The 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 کاملAnomalous 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 کاملAnomalous left coronary artery from pulmonary artery (ALCAPA) in asymptomatic 11-year-old case
Sum mary Origin of the left coronary artery from the pulmonary trunk [Anomalous origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA)] is a rare congenital heart defect. ALCAPA is one of the common causes of myocardial ischemia or infarction in infants and children. In this report, we present an eleven-years-old patient presenting with murmur and accompanied by echocardiographic...
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 left coronary artery from the pulmonary arteryin an adult.
Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital heart defect that usually presents before the age of 1 year. Several surgical options exist for the correction of ALCAPA; however, debate continues regarding the optimal repair technique in adult populations. We report the case of successful surgical repair of ALCAPA with a direct aortic implantation techniqu...
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ژورنال
عنوان ژورنال: Journal of Rare Cardiovascular Diseases
سال: 2013
ISSN: 2300-5505,2299-3711
DOI: 10.20418/jrcd.vol1no5.19