Soft tissue sarcoma
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| Soft tissue sarcoma | |
| ICD-9 | 171 |
|---|---|
| DiseasesDB | 31472 |
| MeSH | D012509 |
Template:Soft tissue sarcoma Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Treatment
- Surgery is the most common treatment for soft tissue sarcomas. If possible, the doctor will remove the cancer and a safe margin of the healthy tissue around it. Depending on the size and location of the sarcoma, it may occasionally be necessary to remove all or part of an arm or leg (amputation). However, the need for amputation rarely arises; no more than 10 % to 15 % of individuals with sarcoma undergo amputation. In most cases, limb-sparing surgery is an option to avoid amputating the arm or leg. It is important to obtain a margin free of tumor to decrease the likelihood of local recurrence and give the best chance for eradication of the tumor.
- Radiation therapy (treatment with x-rays or radioactive implants) may be used either before surgery to shrink tumors or after surgery to kill any cancer cells that may have been left behind. In some cases, it can be used to treat tumours that cannot be surgically removed. In multiple studies, radiation therapy has been found to improve the rate of local control, but has not had any influence on overall survival.
References
External links
- http://www.cancer.gov/cancertopics/factsheet/Sites-Types/soft-tissue-sarcoma National Cancer Institute Factsheet
- http://www.acor.org/sarcoma-support.html List of ACOR Information & Support Online Communities for sarcomas
- http://cureasps.org/ Cure Alveolar Soft Part Sarcoma International
- http://www.mskcc.org