Massive pericardial effusion due to intrapericardial mixed germ cell tumor in a premature baby


DOKSOZ O., TEREK D. T. , KARACELIK M., YILDIRIM H. T. , DEMIRAG B., MESE T., ...Daha Fazla

PEDIATRICS INTERNATIONAL, cilt.57, ss.968-970, 2015 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 57 Konu: 5
  • Basım Tarihi: 2015
  • Doi Numarası: 10.1111/ped.12655
  • Dergi Adı: PEDIATRICS INTERNATIONAL
  • Sayfa Sayıları: ss.968-970

Özet

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.