Publication Date

12-18-2024

Journal

JACC: Case Reports

DOI

10.1016/j.jaccas.2024.102922

PMID

39822627

PMCID

PMC11734063

PubMedCentral® Posted Date

12-18-2024

PubMedCentral® Full Text Version

Post-print

Published Open-Access

yes

Keywords

congenital heart disease, fetal mass, intracardiac tumor, right atrial mass

Abstract

Fetal and neonatal cardiac tumors are rare and often benign. Clinical presentation is primarily related to mass effect, pericardial effusion or arrhythmia. Prenatal detection can assist with risk assessment and inform optimal delivery plan and postnatal management. We report a fetus with a right atrial mass discovered in the third trimester. After successful surgical resection, pathology confirmed the mass to be a capillary-venous malformation, which are rare and challenging to diagnose. The true incidence of these vascular malformations within cardiac spaces is difficult to discern given the historic classification of numerous different vascular malformations under the umbrella term hemangioma.

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