作者: Zekai Avci , İbrahim Safa Kaya , A Selman Doğukan , O¨ zgür Aydin , O¨ zgür İsmailoğlu
关键词: Brain neoplasm 、 Neoplasm 、 Pathology 、 Mesenchymal stem cell 、 Central nervous system 、 Nervous system 、 Atypical teratoid rhabdoid tumor 、 Pathological 、 Medicine 、 Poor prognosis
摘要: Atypical teratoid/rhabdoid tumor (AT/RT) is extremely malignant, highly aggressive primitive central nervous systemneoplasm of infancy with very poor prognosis. Histologically, AT/RT defined as a polymorphous neoplasm often featuring rhabdoid, PNET, mesenchymal, and epithelial components. We report the clinical history, radioligical, pathological findings in child affected bycentral system AT/RT.