Djordjevic, Stefan A. (57192951203)Stefan A. (57192951203)DjordjevicGlumac, Sofija (33467624700)Sofija (33467624700)GlumacKalanj, Jasna (8405619200)Jasna (8405619200)Kalanj2025-06-122025-06-122017https://doi.org/10.1017/S1047951116002699https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009366170&doi=10.1017%2fS1047951116002699&partnerID=40&md5=71508cbabd0eb122e82091370b370c15https://remedy.med.bg.ac.rs/handle/123456789/6887Cardiac 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.Cardiac tumourcongenital haemangiomapulmonary atresiatransposition of the great arteriestricuspid atresia