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Anomalous origin of the left coronary artery from the pulmonary artery, scimitar syndrome, and aortic coarctation

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dc.contributor.authorIlic, Slobodan (57212487618)
dc.contributor.authorHercog, Djordje (8252832000)
dc.contributor.authorVucicevic, Milan (8252832100)
dc.contributor.authorVulicevic, Irena (55588791200)
dc.contributor.authorMimic, Branko (55891059600)
dc.contributor.authorDjukic, Milan (23988377500)
dc.contributor.authorJovanovic, Ida (23989306000)
dc.contributor.authorParezanovic, Vojislav (14325763000)
dc.contributor.authorIlisic, Tamara (8285901300)
dc.date.accessioned2025-06-12T20:14:58Z
dc.date.available2025-06-12T20:14:58Z
dc.date.issued2014
dc.description.abstractAnomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) represents one of the most common causes of myocardial ischemia in infants and if left untreated results in a high mortality rate. When ALCAPA coexists with other congenital malformations, particularly those associated with pulmonary hypertension, the initial presentation can be quite confusing and is often misinterpreted. We report an infant with ALCAPA associated with scimitar syndrome and aortic coarctation whose clinical course illustrates the complexities and difficulties of management with a successful outcome. © 2014 by The Society of Thoracic Surgeons Published by Elsevier Inc.
dc.identifier.urihttps://doi.org/10.1016/j.athoracsur.2013.05.109
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84893412733&doi=10.1016%2fj.athoracsur.2013.05.109&partnerID=40&md5=3d09233e74eb72ec9f2531c6758f0ee1
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/8616
dc.subject20
dc.subjectCTSNet classification
dc.titleAnomalous origin of the left coronary artery from the pulmonary artery, scimitar syndrome, and aortic coarctation
dspace.entity.typePublication

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