Anomalous left coronary artery

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Anomalous Left Coronary Artery Arising

ANGIOCARDIOGRAPHY has recently led to the recognition of the anomalous left coronary artery arising from the pulmonary artery in older children and adolescents. Three 16-year old patients are the oldest ones in whom the diagnosis has been made during life.'In all of the 14 cases4-6 reported from the adult age group (18 years or more) the diagnosis was made at autopsy. We are reporting here a mi...

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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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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-...

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Anomalous origin of left coronary artery from the left ventricle.

A 54-year-old asymptomatic woman (M.H.S.), was referred to the Hospital das Clínicas da Universidade Federal de Minas Gerais (HC/UFMG) cardiology service for routine cardiological evaluation in 2006. The physical examination and basal ECG were normal. Exercise stress testing showed unspecific ST segment alteration, and technetium scintigraphy was normal. One year later, repeat examination showe...

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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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ژورنال

عنوان ژورنال: The Journal of Thoracic and Cardiovascular Surgery

سال: 1973

ISSN: 0022-5223

DOI: 10.1016/s0022-5223(19)40720-4