Chordoma natural history: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
Line 15: | Line 15: | ||
[[Category:Disease]] | [[Category:Disease]] | ||
[[Category:Types of cancer]] | [[Category:Types of cancer]] | ||
{{WikiDoc Help Menu}} | {{WikiDoc Help Menu}} | ||
{{WikiDoc Sources}} | {{WikiDoc Sources}} |
Latest revision as of 14:52, 18 August 2015
Please help WikiDoc by adding more content here. It's easy! Click here to learn about editing.
Chordoma Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Chordoma natural history On the Web |
American Roentgen Ray Society Images of Chordoma natural history |
Risk calculators and risk factors for Chordoma natural history |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Natural History
Complications
Prognosis
In one study, the 10-year tumor free survival rate for sacral chordoma was 46%.[1] Chondroid chordomas appear to have a more indolent clinical course.
References
- ↑ Fuchs B, Dickey ID, Yaszemski MJ, Inwards CY, Sim FH (2005). "Operative management of sacral chordoma". The Journal of bone and joint surgery. American volume. 87 (10): 2211–6. doi:10.2106/JBJS.D.02693. PMID 16203885.