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

Published online by Cambridge University Press:  12 January 2017

Stefan A. Djordjevic ,
Sofija Glumac  and
Jasna Kalanj
Stefan A. Djordjevic*
Affiliation:
Department of Cardiology, University Children’s Hospital, Belgrade, Serbia
Sofija Glumac
Affiliation:
Institute of Pathology, School of Medicine, University of Belgrade, Belgrade, Serbia
Jasna Kalanj
Affiliation:
Pediatric and Neonatal Intensive Care Unit, University Children’s Hospital, Belgrade, Serbia
*
Correspondence to: S. A. Djordjevic, Department of Cardiology, University Children’s Hospital, 10 Tirsova Street, 11000 Belgrade, Serbia. Tel: +381 11 2060 715; Fax: +381 11 2684 672; E-mail: [email protected]
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Abstract

Cardiac 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.

Keywords

Cardiac tumourcongenital haemangiomatricuspid atresiapulmonary atresiatransposition of the great arteries
Type
Brief Report
Information
Cardiology in the Young , Volume 27 , Issue 5 , July 2017 , pp. 990 - 992
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Copyright
© Cambridge University Press 2017 

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