MAJOR AORTOPULMONARY COLLATERAL ARTERY NOMENCLATURE
نویسندگان
چکیده
منابع مشابه
Ruptured giant major aortopulmonary collateral artery.
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . doi:10.1093/eurheartj/ehs317 Online publish-ahead-o...
متن کاملPrenatal diagnosis of major aortopulmonary collateral arteries.
BACKGROUND The presence of foetal major aortopulmonary collateral arteries (MAPCAs) is associated with adverse outcome, therefore early diagnosis is essential. AIM To evaluate the usefulness of foetal echocardiography in the diagnosis and evaluation of MAPCAs in foetuses with pulmonary atresia, as well as to assess the effects of prenatal diagnosis on the management of neonates with pulmonary...
متن کاملIsolated major aortopulmonary collateral artery in an infant presenting with recurrent lower respiratory tract infection.
To cite: Patra S, Srinivas SK, Agrawal N, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2013200421 DESCRIPTION A 5-month-old baby, weighing 4 kg presented with a 3-month history of failure to thrive and recurrent lower respiratory tract infection (RTI). She was delivered at term weighing 2.8 kg and the perinatal period was uneventful. Saturation and clini...
متن کاملGiant major aortopulmonary collateral artery: a rare cause of heart murmur in newborns.
Major aortopulmonary collateral arteries (MAPCAs) are anomalous vessels that develop from the aorta or its main branches and supply the pulmonary parenchyma with oxygenated blood. They are usually associated with congenital heart disease and are rare in isolation. We report the case of a newborn girl, full term, with no relevant history, in whom a III/VI murmur was detected on the left sternal ...
متن کاملRotational ablation assisted angioplasty of an obstructed aortopulmonary collateral artery.
A 15 month old baby girl with pulmonary atresia, ventricular septal defect, and multiple aortopulmonary collateral arteries underwent rotational ablation assisted balloon angioplasty of a severely stenosed collateral artery that had previously proved undilatable using a high pressure non-compliant balloon angioplasty catheter. It is postulated that the rotablation debulked a fibrotic stricture ...
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ژورنال
عنوان ژورنال: Journal of the American College of Cardiology
سال: 2013
ISSN: 0735-1097
DOI: 10.1016/s0735-1097(13)60543-4