Publication | Closed Access
Soft Tissue Sarcoma
166
Citations
490
References
2010
Year
Soft Tissue SurgerySurgical OncologyTumoral PathologySoft Tissue SarcomaGastrointestinal OncologyFrequent SarcomasMedicineSurgical PathologyHistopathologyGastroenterologyPathologyGastrointestinal Stromal TumorsAnnual IncidenceSurgeryBone.soft Tissue SarcomasOncologyMalignant DiseaseCancer Research
OverviewSarcomas constitute a heterogeneous group of rare solid tumors of mesenchymal cell origin with distinct clinical and pathological features, and are usually divided into 2 broad categories: sarcomas of soft tissues (including fat, muscle, nerve and nerve sheath, blood vessels, and other connective tissues) and sarcomas of bone.Soft tissue sarcomas (STS) are the most frequent sarcomas; the annual incidence in the United States for 2009 is estimated to be approximately 10,660 cases, with an overall mortality rate of approximately 3820 cases per year, including adults and children. 1 The true incidence of sarcoma is underestimated, especially because a large proportion of patients with gastrointestinal stromal tumors (GIST) may not
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