A Case of Fetal Intracardiac Tumor Detected on Fetal Echocardiography.
- Author:
Jae Sung SON
1
Author Information
1. Department of Pediatrics, College of Medicine, Dankook University, Cheonan, Korea.
- Publication Type:Case Report
- Keywords:
Fetal echocardiography;
Rhabdomyoma;
Cardiac tumor
- MeSH:
Arrhythmias, Cardiac;
Autopsy;
Echocardiography*;
Fetus;
Fibroma;
Heart;
Heart Neoplasms;
Hemodynamics;
Humans;
Infant, Newborn;
Rhabdomyoma;
Teratoma;
Tuberous Sclerosis
- From:Journal of the Korean Pediatric Cardiology Society
2005;9(1):188-192
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Primary tumors of the heart are uncommon in the fetus and neonate and are most often histologically benign. Rhabdomyoma is the most common cardiac tumor in the fetus and pediatric population which is followed in frequency by fibroma and teratoma. Rhabdomyomas are usually multiple, solid, and lobulated and an estimated 50-86% of rhabdomyoma cases are associated with tuberous sclerosis. Since spontaneous regression of rhabdomyoma is well documented, surgical intervention is recommended only for those patients with severe hemodynamic compromise or for those with persistent arrhythmias. A case of rhabdomyoma detected by fetal echocardiography, which was proved by autopsy, is reported.
