Synovial sarcoma natural history, complications and prognosis: Difference between revisions
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== Prognosis == | == Prognosis == | ||
Despite treatment, prognosis is generally poor, with approximately 50% of patients dying from local reccurrence or [[metastasis]] within 10 years. | Despite treatment, prognosis is generally poor, with approximately 50% of patients dying from local reccurrence or [[metastasis]] within 10 years. | ||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} | ||
[[Category:Disease]] | [[Category:Disease]] | ||
Latest revision as of 19:56, 28 August 2015
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Natural History
synovial sarcoma is a misnomer and the origin of the tissue is unknown. Primary synovial sarcomas have been documented in most human tissues and organs, including the brain, prostate and heart. Synovial sarcoma occurs most commonly in adolescents and young adults.
Prognosis
Despite treatment, prognosis is generally poor, with approximately 50% of patients dying from local reccurrence or metastasis within 10 years.