Abstract
Musculoskeletal sarcomas represent a heterogeneous group of malignancies involving bone and soft tissue with a highly variable natural history and a correspondingly diverse range of potential therapeutic strategies. The choice of treatment is largely driven by prognostic factors but is also dependent on local expertise, resources, and philosophies and the particular clinical circumstances of individual patients. Important considerations include the type, grade, extent, and location of the tumor. Curative treatment approaches in osteogenic sarcoma combine surgery and chemotherapy. In Ewing sarcoma, chemotherapy is used, and local control is achieved by surgery, radiotherapy, or a combination of both (1-3).
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Howman-Giles, R., Hicks, R.J., McCowage, G., Chung, D.K. (2006). Primary Bone Tumors. In: Charron, M. (eds) Pediatric PET Imaging. Springer, New York, NY. https://doi.org/10.1007/0-387-34641-4_15
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DOI: https://doi.org/10.1007/0-387-34641-4_15
Publisher Name: Springer, New York, NY
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