Prenatally evolving ectopia cordis with successful surgical treatment.

Abstract:

:Ectopia cordis (EC) is a rare malformation due to failure of maturation of the midline mesodermal components of the chest and abdomen. It can be defined as a complete or partial displacement of the heart outside the thoracic cavity. It comprises 0.1% of congenital heart diseases. Common cardiac anomalies associated with EC are ventricular septal defect, atrial septal defect, and tetralogy of Fallot. EC and additional anomalies usually lead to intrauterine death. The possibility and efficacy of surgery in a surviving neonate depends on the degree of EC, coexisting congenital heart defects and extracardiac malformations. We present a case of prenatally diagnosed isolated EC diagnosed in the first half of pregnancy. After counseling, the patient decided to continue her pregnancy which ended with a newborn baby discharged from the hospital after cardiac surgery performed just after elective cesarean section.

journal_name

Fetal Diagn Ther

authors

Sadłecki P,Krekora M,Krasomski G,Walentowicz-Sadłecka M,Grabiec M,Moll J,Respondek-Liberska M

doi

10.1159/000326300

subject

Has Abstract

pub_date

2011-01-01 00:00:00

pages

70-2

issue

1

eissn

1015-3837

issn

1421-9964

pii

000326300

journal_volume

30

pub_type

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