Soft tissue sarcoma epidemiology and demographics: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{Soft tissue sarcoma}} | {{Soft tissue sarcoma}} | ||
{{CMG}} | {{CMG}} | ||
==Overview== | ==Overview== | ||
Soft tissue sarcomas are relatively uncommon cancers. They account for less than 1 % of all new cancer cases each year. | Soft tissue sarcomas are relatively uncommon cancers. They account for less than 1% of all new cancer cases each year.<ref name="pmid9344316">{{cite journal| author=Zahm SH, Fraumeni JF| title=The epidemiology of soft tissue sarcoma. | journal=Semin Oncol | year= 1997 | volume= 24 | issue= 5 | pages= 504-14 | pmid=9344316 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9344316 }} </ref> | ||
==Epidemiology== | ==Epidemiology== | ||
===Incidence=== | |||
In 2006, about 9,500 new cases were diagnosed in the United States.<ref>Ries LAG, Harkins D, Krapcho M, et al. SEER Cancer Statistics Review, 1975–2003. Bethesda , MD: National Cancer Institute, 2006.</ref> | In 2006, about 9,500 new cases were diagnosed in the United States.<ref>Ries LAG, Harkins D, Krapcho M, et al. SEER Cancer Statistics Review, 1975–2003. Bethesda , MD: National Cancer Institute, 2006.</ref> | ||
===Age=== | ===Age=== | ||
Revision as of 00:58, 17 June 2014
Template:Soft tissue sarcoma Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Soft tissue sarcomas are relatively uncommon cancers. They account for less than 1% of all new cancer cases each year.[1]
Epidemiology
Incidence
In 2006, about 9,500 new cases were diagnosed in the United States.[2]
Age
Soft tissue sarcomas are more commonly found in older patients (>50 years old) although in children and adolescents under age 20, certain histologies are common (rhabdomyosarcoma).
Percent Distribution of Soft Tissue Sarcoma by Histology
- Fibrosarcoma: 6.9%
- Infantile fibrosarcoma: 0.2%
- Fibrous histiocytoma, malignant: 9.2%
- Dermatofibrosarcoma: 3.6%
- Liposarcoma: 17.1%
- Leiomyosarcoma: 13.2%
- Rhabdomyosarcoma: 3.1%
- Embryonal rhabdomyosarcoma: 1.3%
- Hemangiosarcoma: 3.7%
- Hemangiopericytoma, malignant: 0.5%
- Kaposi sarcoma: 0.8%
- Malignant peripheral nerve sheath tumor: 1.6%
- Malignant neurilemmoma: 0.2%
- Neuroblastoma: 0.6%
- Synovial sarcoma: 4.8%
References
- ↑ Zahm SH, Fraumeni JF (1997). "The epidemiology of soft tissue sarcoma". Semin Oncol. 24 (5): 504–14. PMID 9344316.
- ↑ Ries LAG, Harkins D, Krapcho M, et al. SEER Cancer Statistics Review, 1975–2003. Bethesda , MD: National Cancer Institute, 2006.