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Bone and Soft Tissue Cancer

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Manual of Clinical Oncology

Part of the book series: UICC International Union Against Cancer ((UICCI))

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Abstract

Bone tumors are relatively rare. Their incidence varies according to age. While the frequency of osteogenic sarcoma and Ewing’s sarcoma is higher in adolescents than in adults, the opposite is true for chondrosarcoma. The incidence of Ewing’s sarcoma among blacks is about 10% of the incidence among white children and adolescents. Benign bone tumors (osteomas, chondromas, benign bone-forming lesions) occur in both young and adult patients and must not be mistaken for sarcomas.

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References and Further Reading

  • Lemerle J ed (1989) Cancer de l’enfant. Flammarion, Paris

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  • NIH (1985) Consensus development panel on limb-sparing treatment. Cancer treatment symposia, vol 3

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  • Spiessl B, Scheibe O, Wagner G (eds) (1982) TNM-Atlas. Springer, Berlin Heidelberg New York

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  • Voute PA, Barrett A, Bloom HJG et al. (eds) (1986) Cancer in children, 2nd edn. Springer, Berlin Heidelberg New York

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© 1982 Springer-Verlag Berlin Heidelberg

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Voûte, P.A., Hossfeld, D.K. (1982). Bone and Soft Tissue Cancer. In: Sherman, C.D., Hossfeld, D.K., Love, R.R., Bosch, F.X. (eds) Manual of Clinical Oncology. UICC International Union Against Cancer. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-97267-6_32

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  • DOI: https://doi.org/10.1007/978-3-642-97267-6_32

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-52769-5

  • Online ISBN: 978-3-642-97267-6

  • eBook Packages: Springer Book Archive

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