| Literature DB >> 16534791 |
Hiroyoshi Watanabe1, Tsutomu Watanabe, Michiya Kaneko, Hiroko Suzuya, Toshihiro Onishi, Yasuhiro Okamoto, Hajime Miyake, Kensaku Yasuo, Takanori Hirose, Shoji Kagami.
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. (c) 2006 Wiley-Liss, Inc.Entities:
Mesh:
Year: 2006 PMID: 16534791 DOI: 10.1002/pbc.20699
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167