Congenitally corrected transposition of the great arteries

Seon-Hye Kim1,2, Mamoru Tanaka3, Momo Umezu3

  • 1Department of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo, Japan. kim-sh@kmh.gr.jp.

Insights

Congenitally corrected transposition of the great arteries (cTGA) is a rare heart defect. This case highlights prenatal diagnosis of cTGA using specific imaging views, even without other cardiac anomalies.

Area of Science:

  • Cardiology
  • Medical Imaging
  • Fetal Medicine

Background:

  • Congenitally corrected transposition of the great arteries (cTGA) is an uncommon congenital heart malformation.
  • cTGA involves discordant atrioventricular and ventriculoarterial connections, often with associated anomalies.
  • Prenatal detection of cTGA can be challenging due to subtle presentations and mimicry of other conditions like complete TGA.

Purpose of the Study:

  • To report a case of in utero diagnosis of cTGA.
  • To emphasize the diagnostic utility of specific echocardiographic views for cTGA.
  • To highlight the importance of identifying cTGA prenatally, even in the absence of other cardiac defects.

Main Methods:

  • Fetal echocardiography at 29 weeks' gestation.
  • Detailed examination of the four-chamber view to assess atrioventricular connections.
  • Assessment of the spatial relationship of the great vessels.

Main Results:

  • A diagnosis of cTGA was made prenatally at 29 weeks' gestation.
  • No additional cardiac anomalies were identified prenatally.
  • Postnatal findings included a patent ductus arteriosus with bidirectional flow.

Conclusions:

  • Accurate prenatal diagnosis of cTGA is possible with careful echocardiographic assessment.
  • Identifying atrioventricular discordance and the parallel course of great vessels (l-transposition) are key.
  • Early prenatal diagnosis of cTGA facilitates timely postnatal management.