Chondrosarcoma natural history: Difference between revisions
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{{Chondrosarcoma}} | {{Chondrosarcoma}} | ||
==Overview== | |||
==Complications== | |||
Chondrosarcoma may return and may need treatment with [[surgery]], [[chemotherapy]] or [[radiation]]. | |||
==Prognosis== | |||
*Generally, chondrosarcoma carries a good prognosis. | |||
*Chondrosarcoma is associated with a 5 year survival rate of 75%. | |||
*Depending upon the subtype, prognosis vary substantially: | |||
**Chondrosarcoma NOS and myxoid chondrosarcoma have a five year survival of approximately 70%. | |||
**Mesenchymal chondrosarcoma have a 5 year survival of approximately 50%. | |||
**Dedifferentiated chondrosarcoma have a 5 year survival of 0%. | |||
==References== | ==References== | ||
Revision as of 17:43, 28 August 2015
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Chondrosarcoma Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Chondrosarcoma natural history On the Web |
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American Roentgen Ray Society Images of Chondrosarcoma natural history |
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Risk calculators and risk factors for Chondrosarcoma natural history |
Overview
Complications
Chondrosarcoma may return and may need treatment with surgery, chemotherapy or radiation.
Prognosis
- Generally, chondrosarcoma carries a good prognosis.
- Chondrosarcoma is associated with a 5 year survival rate of 75%.
- Depending upon the subtype, prognosis vary substantially:
- Chondrosarcoma NOS and myxoid chondrosarcoma have a five year survival of approximately 70%.
- Mesenchymal chondrosarcoma have a 5 year survival of approximately 50%.
- Dedifferentiated chondrosarcoma have a 5 year survival of 0%.