Ectopia cordis: a case report

• Autor(a) principal: Dias,Gonçalo Filipe Infante Mesquita
• Data de Publicação: 2014
• Outros Autores: Santos,Ana Vanessa dos Reis, Martins,Cátia Filipa Cabrita Paixão, Ferreira,Ana Paula Duarte, Fonseca,Joaquim Marques Dinis da
• Tipo de documento: Relatório
• Idioma: eng
• Título da fonte: Revista Brasileira de Saúde Materno Infantil (Online)
• Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1519-38292014000300287
• topic: Ectopia cordis; Heart defects congenital; Prenatal diagnosis; Ultrasonography

Introduction: ectopia cordis is a rare congenital malformation, with an estimated incidence of 5 to 8 per million live births. It is defined as a malformation in which the heart is located in an extra-thoracic position. Ectopia cordis may occur as an isolated malformation or associated with other anomalies such as omphalocele, congenital heart disease or integrating Cantrell syndrome. The size and location of the defect influence the prognosis. Description: we report a case of a 24-year-old nulliparous woman, with no relevant family or personal history, in which the prenatal fetal ultrasound, performed at 21 weeks of gestation, revealed adefect of the anterior chest wall with exteriorization of the heart. Discussion: fetal echocardiography revealed a severe congenital heart disease. The parents decided to continue the pregnancy, after being duly informed by a multidisciplinary team. Delivery occurred at 37 weeks of gestation but the female newborn died one hour afterwards. Pathological examination confirmed the sonographic findings.