Pediatr Radiol

. 2024 May 16.

 doi: 10.1007/s00247-024-05938-0. Online ahead of print. https://pubmed.ncbi.nlm.nih.gov/38750327/ https://pubmed.ncbi.nlm.nih.gov/38750327/

Ultrasound and computed tomography angiography diagnosis of fetal right atrial isomerism with cardiac total anomalous pulmonary venous connection and intestinal malrotation: a case report and literature review

Junxia Gao ¹, Hongping Ou ¹, Hui Xing ², Hui Chen ³, Yanli Huang ², Feng Cao ³, Yu Wang ⁴

Affiliations expand

• PMID: 38750327
• DOI: 10.1007/s00247-024-05938-0

Abstract

Right atrial isomerism is a rare and severe isomerism. It is frequently associated with complex congenital heart disease and various extracardiac anomalies. Imaging diagnosis of right atrial isomerism is a challenge. Multisystem and complex anomalies in a 24-week-old fetus were diagnosed with prenatal ultrasound, postnatal computed tomography angiography (CTA), and autopsy. The ultrasound detected most major cardiovascular anomalies including right atrial isomerism and total anomalous pulmonary venous connection. The CTA further detected thoracic and abdominal malformations such as bilateral morphologically right bronchus, diaphragmatic hernia, asplenia, midline liver, and intestinal malrotation. The autopsy confirmed both ultrasound and CTA findings with additional findings, namely, bilateral trilobed lungs and bilateral morphological right auricles. Prenatal ultrasound and postnatal CTA can be complementary to each other in detecting multi-system complex anomalies. Their combined use can be useful for prenatal counseling and postpartum management.

Keywords: Autopsy; Computed tomography angiography; Fetus; Hernia, diagphragmatic; Heterotaxy syndrome; Isomerism; Ultrasonography, prenatal.

© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.