Avci Zekai, Kaya Ibrahim Safa, Doğukan A Selman, Aydin Ozgür, Ismailoğlu Ozgür
Department of Pediatrics, Fatih University Faculty of Medicine, Ankara, Turkey.
Pediatr Pathol Mol Med. 2003 Sep-Oct;22(5):443-7.
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, radiological, and pathological findings in a child affected bycentral nervous system AT/RT.
非典型畸胎样/横纹肌样瘤(AT/RT)是一种极其恶性、侵袭性很强的婴幼儿原发性中枢神经系统肿瘤,预后极差。在组织学上,AT/RT被定义为一种多形性肿瘤,常具有横纹肌样、原始神经外胚层肿瘤(PNET)、间充质和上皮成分。我们报告了一名患有中枢神经系统AT/RT儿童的临床病史、影像学和病理学检查结果。