CLINICAL SUMMARY
Synovial sarcoma is the fourth or fifth most common subtype of soft tissue sarcoma and is distinguished by its younger age of presentation, frequent history of pain, and diagnostic chromosomal translocation. While the need for surgical wide resection and optional radiotherapy is analogous to that in other soft tissue sarcomas, the use of chemotherapy for large, deep synovial sarcomas appears to be more clearly associated with improved survival.
DIAGNOSTIC FEATURES
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IMAGING
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