| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4116304 | International Journal of Pediatric Otorhinolaryngology Extra | 2008 | 4 Pages |
Abstract
SummarySynovial sarcoma is a rare malignant non-rhabdomyosarcomatous soft-tissue sarcoma in children and adolescents. Only 4% of synovial sarcoma cases develop in the head and neck. Herein, we described a 10-year-old girl with synovial sarcoma of her right masseter muscle. The diagnosis of synovial sarcoma was confirmed by the existence of SYT-SSX fusion gene transcripts, and she was treated with neoadjuvant and adjuvant chemotherapy, surgical resection and postoperative radiotherapy, though standard treatment for synovial sarcoma is complete surgical resection. She remains free of disease 12 months after treatment, and her right masseter muscle has been normal cosmetically and functionally.
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Authors
Michinori Funato, Hideo Kaneko, Michio Ozeki, Kaori Kanda, Toshiyuki Fukao, Keisuke Mizuta, Naomi Kondo,