Treatment of unresectable malignant rhabdoid tumor of the orbit with tandem high‐dose chemotherapy and gamma‐knife radiosurgery
- 13 March 2006
- journal article
- case report
- Published by Wiley in Pediatric Blood & Cancer
- Vol. 47 (6) , 846-850
- https://doi.org/10.1002/pbc.20699
Abstract
Malignant rhabdoid tumor (MRT) is a rare and highly aggressive tumor that primarily occurs in very young children. We report here a patient with a primary MRT of the orbit who received tandem high‐dose chemotherapy and gamma‐knife radiosurgery. Although the tumor was not completely removed, and the initial chemotherapy failed, the patient achieved long‐term survival after this modality of treatment. This approach may be one to be further considered in patients with MRT. Pediatric Blood Cancer 2006;47:846–850.Keywords
This publication has 17 references indexed in Scilit:
- Malignant Extrarenal Rhabdoid Tumor of the Bladder: 9-Year Survival After Chemotherapy and Partial CystectomyJournal of Urology, 2004
- Cerebral Atypical Teratoid/Rhabdoid Tumor of Infancy: Long-Term Survival after Multimodal Treatment, also Including Triple Intrathecal Chemotherapy and Gamma Knife Radiosurgery--Case ReportPediatric Hematology and Oncology, 2003
- Gamma-knife radiosurgery in pediatric cerebral and skull base tumorsMedical and Pediatric Oncology, 2002
- The role of gamma knife radiosurgery in childrenChild's Nervous System, 2001
- Successful Treatment of a Patient With Stage IV Rhabdoid Tumor of the KidneyJournal of Pediatric Hematology/Oncology, 1999
- Treatment of primary malignant rhabdoid tumor of the brain: report of three cases and review of the literatureInternational Journal of Radiation Oncology*Biology*Physics, 1998
- Central Nervous System Atypical Teratoid Tumor/Rhabdoid Tumor: Response to Intensive Therapy and Review of the LiteratureJournal of Neuro-Oncology, 1998
- Successful Treatment of Disseminated Central Nervous System Malignant Rhabdoid TumorJournal of Pediatric Hematology/Oncology, 1995
- Rhabdoid Tumor of KidneyThe American Journal of Surgical Pathology, 1989
- Histopathology and prognosis of Wilms tumorResults from the first national wilms' tumor studyCancer, 1978