A rare case of cardiac anomaly: prenatally diagnosed ectopia cordis

被引：7

作者：

Celik, Yalcin ^{[1
]}

Hallioglu, Olgu ^{[2
]}

Basut, Nursel ^{[3
]}

Demetgul, Hasan ^{[2
]}

Kibar, A. Esin ^{[4
]}

机构：

[1] Mersin Univ, Tip Fak, Cocuk Sagligi & Hastaliklari Anabilim Dali, Yenidogan Bilim Dali, Mersin, Turkey

[2] Mersin Univ, Tip Fak, Cocuk Sagligi & Hastaliklari Anabilim Dali, Cocuk Kardiyol Bilim Dali, Mersin, Turkey

[3] Mersin Univ, Tip Fak, Cocuk Sagligi & Hastaliklari Anabilim Dali, Mersin, Turkey

[4] Mersin Kadin Dogum & Cocuk Hastaliklari Hastanesi, Cocuk Kardiyol, Mersin, Turkey

来源：

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS | 2015年 / 50卷 / 02期

关键词：

Pentalogy of Cantrell; Ectopia cordis; midline developmental anomalies;

D O I：

10.5152/tpa.2015.927

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Ectopia cordis is a rare congenital malformation in which the heart is located partially or totally outside the thoracic cavity. The estimated prevalence of ectopia cordis is 5.5-7.9 per million births and it comprises 0.1% of congenital heart diseases. Ectopia cordis is associated with other congenital heart diseases and various tissue and organ disorders. Common cardiac anomalies associated with ectopia cordis include ventricular septal defect, atrial septal defect, pulmonary stenosis, right ventricular diverticulum, double right ventricular outflow tract and tetralogy of Fallot. Extracardiac anomalies associated with ectopia cordis reported in the literature include omphalocele, gastrochisis, cleft lip and palate, scollosis and central nervous system malformations. Here we report a newborn with ectopia cordis who was diagnosed prenatally.

引用

页码：129 / 131

页数：3

共 12 条

[1] Complete thoracic ectopia cordis [J].