Atipical teratoid rhabdoid tumor: Case report and review of the literature Atipik teratoid rabdoid tümör: Olgu sunumu ve literatürün derlenmesi
Turk Onkoloji Dergisi, cilt.29, sa.1, ss.15-20, 2014 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 29 Sayı: 1
- Basım Tarihi: 2014
- Doi Numarası: 10.5505/tjoncol.2014.1097
- Dergi Adı: Turk Onkoloji Dergisi
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Sayfa Sayıları: ss.15-20
- Bursa Uludağ Üniversitesi Adresli: Evet
Özet
Atipical teratoid rhabdoid tumor (ATRT) is a rare and highly agressive malign tumor in the early childhood. Mean survival has been reported as 6-11 months. Despite the optimal treatment is unclear surgery, chemotherapy and radiotherapy are the well known treatment options. We would like to report a 4 year old boy who had the diagnosis of ATRT at the temporooccipital region to make a contribution to the literature. © 2014 Turkish Society for Radiation Oncology.