Abstract
Soft tissue sarcoma is a rare type of cancer that begins in the tissues that connect, support, and surround other body structures. This includes muscle, fat, blood vessels, nerves, tendons, and the lining of your joints.
More than 50 subtypes of soft tissue sarcoma exist. Some types are more likely to affect children, while others affect mostly adults. These tumors can be difficult to diagnose because they may be mistaken for many other types of growths.Soft tissue sarcoma can occur anywhere in your body, but the most common types occur in the arms and legs, and in the abdomen. Surgical removal is the most common treatment, although radiation and chemotherapy also may be recommended-depending on the size, type, location and aggressiveness of the tumor.
Publisher
Mapsci Digital Publisher OPC Pvt. Ltd.
Reference11 articles.
1. Enzinger FM, Weiss SW. Soft Tissue Tumors. St Louis, Mosby. Second Edition.1989.
2. Boring CC, Squires TS, Tong T. Cancer statistics. CA Cancer J Clin. 1991;41(1):19-36. PubMed | CrossRef
3. Eriksson M, Hardell L, Berg NO, Möller T, Axelson O. Soft-tissue sarcomas and exposure to chemical substances: a case-referent study. Br J Ind Med. 1981;38(1):27-33. PubMed | CrossRef
4. Wiklund K, Holm LE. Soft tissue sarcoma risk in Swedish agricultural and forestry workers. J Natl Cancer Inst. 1986;76(2):229-34. PubMed
5. Greenwald P, Kovasznay B, Collins DN, Therriault G. Sarcomas of soft tissues after Vietnam service. J Natl Cancer Inst. 1984;73(5):1107-9. PubMed