Pathology teach and tell: Central nervous system atypical teratoid/rhabdoid tumor

Avci Z., Kaya I., Dogukan A., Aydin O., Ismailoglu O.

PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE, cilt.22, sa.5, ss.443-447, 2003 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 22 Sayı: 5
  • Basım Tarihi: 2003
  • Doi Numarası: 10.1080/15227950307706
  • Dergi Adı: PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.443-447
  • Hacettepe Üniversitesi Adresli: Hayır

Özet

Atypical teratoid/rhabdoid tumor (AT/RT) is extremely malignant, highly aggressive primitive central nervous systemneoplasm of infancy with very poor prognosis. Histologically, AT/RT is defined as a polymorphous neoplasm often featuring rhabdoid, PNET, mesenchymal, and epithelial components. We report the clinical history, radioligical, and pathological findings in a child affected bycentral nervous system AT/RT.