Abstract
Tumors of the soft tissue and bone, classified as mesenchymal tumors, are relatively rare; the annual incidence in the United States is fewer than 5,000 cases. A major proportion of these tumors occur in the pediatric age group in the form of osteogenic or other bone sarcomas and rhabdomyo sarcomas. The adult types of sarcomas are the soft tissue variants, dominated by the malignant fibrohistiocytoma. The natural history and clinical behavior of the various categories of soft tissue sarcomas are related to the stage and histologic grade of the tumor, site of the primary tumor and, to some extent, the pathologic subtype.
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Lokich, J.J., Lackman, R., Weiss, A.J. (1987). Soft Tissue and Osteogenic Sarcomas. In: Cancer Chemotherapy by Infusion. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-3193-0_29
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DOI: https://doi.org/10.1007/978-94-009-3193-0_29
Publisher Name: Springer, Dordrecht
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