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一名新生儿中与导管依赖性先天性心脏病相关的心脏血管瘤。

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

作者信息

Djordjevic Stefan A, Glumac Sofija, Kalanj Jasna

机构信息

1Department of Cardiology,University Children's Hospital,Belgrade,Serbia.

2Institute of Pathology,School of Medicine,University of Belgrade,Belgrade,Serbia.

出版信息

Cardiol Young. 2017 Jul;27(5):990-992. doi: 10.1017/S1047951116002699. Epub 2017 Jan 12.

DOI:10.1017/S1047951116002699
PMID:28077189
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.

摘要

心脏血管瘤极为罕见；然而，它们可导致严重的血流动力学损害和心律紊乱。心脏肿瘤也很少会与先天性心脏病变同时存在。我们报告了一例极为罕见的病例，在大动脉复杂转位的情况下出现心脏血管瘤，导致功能性三尖瓣闭锁。据我们所知，这是文献中首次描述的此类病例。

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