ALCAPA: The Al Capone of coronary artery anomalies

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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...

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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...

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The 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...

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[Coronary artery anomalies].

Coronary artery anomalies (CAAs) are a rare entity but their true incidence in the general population has yet to be determined. Most CAAs are asymptomatic, but they are nevertheless the second leading cause of sudden death in apparently healthy young athletes. The new imaging methods available to cardiologists, including CT angiography and MRI, now enable noninvasive diagnosis and characterizat...

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CLINICAL PROGRESS Coronary Artery Anomalies

CORONARY artery anomalies were formerly regarded as having slight clinical significance. This attitude reflected the little that could be accomplished in the way of diagnosis and treatment. Today, however, recognition seems imperative for four reasons. First, corrective surgery is available in certain instances. Secondly, there are cases in which correction is contraindicated. Thirdly, the pres...

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ژورنال

عنوان ژورنال: South African Journal of Radiology

سال: 2012

ISSN: 2078-6778,1027-202X

DOI: 10.7196/sajr.633