Evaluation of clinical features and outcome of eight fetuses with ectopia cordis; A study from a fetal cardiology center

Congenit Anom (Kyoto). 2023 May;63(3):66-73. doi: 10.1111/cga.12508. Epub 2023 Jan 31.

Abstract

We aim to evaluate the clinical course and outcome of cases with a prenatal diagnosis of ectopia cordis in our center. In this retrospective study, we analyzed clinical variables including gestational age at diagnosis, maternal age, associated cardiac, extracardiac, genetic anomalies and, outcome in prenatally diagnosed ectopia cordis cases in our tertiary referral center. Eight ectopia cordis cases from seven pregnancies were included in the study. All fetuses had complete type of ectopia cordis and pentalogy of Cantrell. Five multiple pregnancies were found, four were twin pregnancies (three dichorionic diamniotic, one monochorionic monoamniotic) and one was triplet (trichorionic triamniotic). In the monochorionic monoamniotic twin pregnancy, both fetuses have pentalogy of Cantrell. Two cases had intracardiac structural defects including Tetralogy of Fallot and hypoplastic right heart syndrome. Three pregnancies were terminated, four cases delivered alive could not survive beyond the neonatal period. The striking feature in our study is its association with multiple pregnancies.

Keywords: ectopia cordis; multiple pregnancies; pentalogy of cantrell; prenatal diagnosis.

MeSH terms

  • Adult
  • Ectopia Cordis* / diagnostic imaging
  • Ectopia Cordis* / pathology
  • Female
  • Fetal Diseases* / diagnostic imaging
  • Fetal Diseases* / pathology
  • Gestational Age
  • Humans
  • Infant, Newborn
  • Pentalogy of Cantrell / diagnostic imaging
  • Pentalogy of Cantrell / pathology
  • Pregnancy
  • Pregnancy Outcome
  • Prenatal Diagnosis
  • Retrospective Studies