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

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

PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE, vol.22, no.5, pp.443-447, 2003 (SCI-Expanded)

• Publication Type: Article / Article
• Volume: 22 Issue: 5
• Publication Date: 2003
• Doi Number: 10.1080/15227950307706
• Journal Name: PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE
• Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
• Page Numbers: pp.443-447
• Hacettepe University Affiliated: No

Abstract

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.