Literature DB >> 26147709

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

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.
© 2015 Japan Pediatric Society.

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


  1 in total

1.  Pericardial effusion as an atypical initial presentation of extra-gonadal nonseminomatous germ cell tumor: a case report and literature review.

Authors:  William Paul Skelton; Dhruv Mahtta; Samantha Welniak; Aaron J Franke; Long H Dang
Journal:  Oxf Med Case Reports       Date:  2018-02-22
  1 in total

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