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Part of the book series: Medical Radiology ((Med Radiol Radiat Oncol))

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Abstract

The incidence of CNS tumors is 7–10 per 100,000 (Parkin and Muir 1992). These include parenchymal tumors as well as other non-CNS intracranial lesions like meningioma. CNS tumors can be organized according to the cell of origin, location, or behavior. Consideration of metastatic lesions provides an additional criterion for organization into primary and secondary lesions. Most presentations and classifications are based on the cell of origin, including the recent classification protocols established by the World Health Organization (WHO) (Kleihues et al. 1993; Burger 1995). The bulk of this chapter is organized according to the cell of origin. The cell of origin is not known for all CNS tumors. The identity of the hemangioblastoma stromal cell, for example, is not known. The bulk of the mature central nervous system cellular population consists of neurons, astrocytes, oligodendrocytes,and ependymal cells. These are all derivatives of the primitive embryona neuroectoderm. The most common intraparenchymal neoplasms arise from the astrocyte and will be discussed first.

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© 2003 Springer-Verlag Berlin Heidelberg

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Atkinson, R. (2003). Pathology of CNS Tumors. In: Petrovich, Z., Brady, L.W., Apuzzo, M.L.J., Bamberg, M. (eds) Combined Modality Therapy of Central Nervous System Tumors. Medical Radiology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-56411-6_2

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  • DOI: https://doi.org/10.1007/978-3-642-56411-6_2

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-00627-5

  • Online ISBN: 978-3-642-56411-6

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