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Introduction to Bone Sarcomas

  • Ioannis D. Papanastassiou
  • Nikolaos S. Demertzis
Chapter

Abstract

Sarcomas are malignant tumors of mesenchymal origin, while carcinomas derive from epithelial cells. They comprise approximately 1% of all malignancies, with soft tissue sarcomas being around 80% off all sarcomas. Bone sarcomas are seen more often in childhood (except chondrosarcomas), while soft tissue sarcomas predominate in the elderly. Since they have distinct features, they will be discussed separately (NCCN Guidelines (2012) Bone cancer. Version 2. www.nccn.org).

References

  1. 1.
    NCCN Guidelines (2012) Bone cancer. Version 2. www.nccn.org
  2. 2.
    Fletcher CDM, Unni KK, Mertens F (2002) World Health Organization Classification of tumours: pathology and genetics of tumours of soft tissue and bone. IARC Press, LyonGoogle Scholar
  3. 3.
    Mankin HJ, Mankin CJ, Simon MA (1996) The hazards of the biopsy, revisited. J Bone Joint Surg Am 78(5):656–663CrossRefGoogle Scholar
  4. 4.
    Simon MA, Aschliman MA, Thomas N, Mankin HJ (1986) Limb Salvage treatment versus amputation for osteosarcoma of the distal end of the femur. J Bone Joint Surg Am 68(9):1331–1337CrossRefGoogle Scholar
  5. 5.
    Theos C, Koulouvaris P, Kottakis S, Demertzis N (2008) Reconstruction of tibia defects by ipsilateral vascularized fibula transposition. Arch Orthop Trauma Surg 128(2):179–184CrossRefGoogle Scholar

Copyright information

© Springer International Publishing AG, part of Springer Nature 2018

Authors and Affiliations

  • Ioannis D. Papanastassiou
    • 1
  • Nikolaos S. Demertzis
    • 1
  1. 1.General Oncological HospitalAthensGreece

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