Complete thoracic ectopia cordis

被引：20

作者：

Alphonso, N ^{[1
]}

Venugopal, PS ^{[1
]}

Deshpande, R ^{[1
]}

Anderson, D ^{[1
]}

机构：

[1] United Med & Dent Sch Guys & St Thomas Hosp, Guys Hosp, Dept Congenital Heart Dis, London SE1 9RT, England

来源：

EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY | 2003年 / 23卷 / 03期

关键词：

thoracic ectopia cordis;

D O I：

10.1016/S1010-7940(02)00811-4

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Thoracic ectopia cordis is a rare congenital defect with very few reported survivors after surgical correction. We report a case of complete thoracic ectopia cordis with double outlet right ventricle. The diagnosis was established antenatally and a repair was undertaken soon after birth. The child remained stable and was extubated on the fifth post-operative day. Forty-eight hours later the child succumbed to an unexplained respiratory arrest. Also presented is a review of the different surgical strategies for this unusual condition. (C) 2003 Elsevier Science B.V. All rights reserved.

引用

页码：426 / 428

页数：3

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