Rhabdomyosarcoma and other soft-tissue sarcomas Book Section


Authors: Fein Levy, C.; Wexler, L. H.
Editors: Lanzkowsky, P.; Lipton, J. M.; Fish, J. D.
Article/Chapter Title: Rhabdomyosarcoma and other soft-tissue sarcomas
Abstract: Soft-tissue sarcomas (STS) are a heterogeneous group of malignant tumors derived from primitive mesenchymal cells. These tumors arise from muscle, connective tissue, supportive tissue, and vascular tissue. As a group, they are locally highly invasive and have a high propensity for local recurrence. They usually metastasize via the bloodstream and, less commonly, via the lymphatics. The STS can be divided into two groups: 1. Rhabdomyosarcoma (RMS). 2. Nonrhabdomyosarcoma soft-tissue sarcomas (NRSTS).
Keywords: relapse; risk; pet; prognostic-factors; radiation-therapy; childrens oncology group
Book Title: Lanzkowsky's Manual of Pediatric Hematology and Oncology. 6th ed
ISBN: 9780128013687
Publisher: Academic Press, Elsevier Inc  
Publication Place: San Diego, CA
Date Published: 2016-05-12
Start Page: 505
End Page: 523
Language: English
ACCESSION: WOS:000411358100033
PROVIDER: wos
DOI: 10.1016/B978-0-12-801368-7.00026-0
Notes: Article; Book Chapter: 26 -- Source: Wos
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  1. Leonard H Wexler
    192 Wexler