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Cardiac haemangioma associated with a duct-dependent congenital heart disease in a newborn infant

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dc.contributor.authorDjordjevic, Stefan A. (57192951203)
dc.contributor.authorGlumac, Sofija (33467624700)
dc.contributor.authorKalanj, Jasna (8405619200)
dc.date.accessioned2025-06-12T17:17:28Z
dc.date.available2025-06-12T17:17:28Z
dc.date.issued2017
dc.description.abstractCardiac haemangiomas are exceedingly rare; however, they can cause significant haemodynamic impairment and disturbances in heart rhythm. Rarely, cardiac tumours may also coexist with congenital heart lesions. We present an extremely unusual case of a cardiac haemangioma in the setting of complex transposition of the great arteries that caused functional tricuspid atresia. To our knowledge, this is the first such case described in the literature. © Cambridge University Press 2017.
dc.identifier.urihttps://doi.org/10.1017/S1047951116002699
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85009366170&doi=10.1017%2fS1047951116002699&partnerID=40&md5=71508cbabd0eb122e82091370b370c15
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/6887
dc.subjectCardiac tumour
dc.subjectcongenital haemangioma
dc.subjectpulmonary atresia
dc.subjecttransposition of the great arteries
dc.subjecttricuspid atresia
dc.titleCardiac haemangioma associated with a duct-dependent congenital heart disease in a newborn infant
dspace.entity.typePublication

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