| Literature DB >> 26147709 |
Önder Doksöz1, Demet Tümay Terek2, Mustafa Karaçelik3, Hülya Tosun Yıldırım4, Bengü Demirağ5, Timur Meşe1, Osman Nejat Sarıosmanoğlu3, Sertaç Arslanoğlu2.
Abstract
Primary cardiac tumor is uncommon in childhood, with an incidence of 0.06-0.32%, and intrapericardial teratoma represents an exceptional rarity among these entities. Germ cell tumors (GCT) are rare, representing only 1-3% of childhood tumors. Twenty per cent of GCT are malignant and are associated with age and location. Extragonadal involvement accounts for nearly half of the cases. Anterior mediastinum is a common location of malignant germ cell tumors, yet pericardial and aortic adventitia involvement have been rarely reported. Here we report the case of a preterm twin baby boy with intrapericardial mixed germ cell tumor who presented with hydrops fetalis and pericardial effusion.Entities:
Keywords: hydrops fetalis; intrapericardial mass; pericardial effusion
Mesh:
Year: 2015 PMID: 26147709 DOI: 10.1111/ped.12655
Source DB: PubMed Journal: Pediatr Int ISSN: 1328-8067 Impact factor: 1.524