Brain Tumor Pathology: Current Diagnostic Hotspots and Pitfalls

  • Davide¬†Schiffer

Table of contents

  1. Front Matter
    Pages i-vi
  2. Pages 1-2
  3. Pages 25-26
  4. Pages 27-58
  5. Pages 59-81
  6. Pages 113-121
  7. Pages 155-160
  8. Pages 171-182
  9. Pages 189-198
  10. Pages 199-209
  11. Back Matter
    Pages 211-272

About this book

Introduction

Since Bailey and Cushing (1926), all brain tumor classifications have been called histogenetic. The nosographic position that the tumor types progressively acquired in the classification systems derived from the resemblance of tumor cells to those of the cytogenesis, modified whenever new information became available from different biological research fields and especially from molecular genetics. Classically, on the basis of the rough correspondence between the mature/immature aspect of tumor cells and the benign/malignant biological behavior of the tumors, the histological labels contained a prognostic significance. The supposed origin of the tumors was thus a factor for prognosis. Later on, with the concept of anaplasia (Cox, 1933; Kernohan et al., 1949) new criteria were introduced for establishing the malignancy grades of tumors. Immunohistochemistry and later molecular genetics further refined the prognostic diagnoses, substantially increasing the opportunities to recognize the cell origin of tumors, beside revealing the pathogenetic mechanisms. Prognoses became more accurate, as required by the greater and more targeted possibilities of therapy.

Keywords

angiogenesis apoptosis biopsy diagnostics glioma

Authors and affiliations

  • Davide¬†Schiffer
    • 1
  1. 1.Neuro-bio oncology Center, Policlinico di Monza FoundationUniversity of TurinItaly

Bibliographic information

  • DOI https://doi.org/10.1007/1-4020-3998-0
  • Copyright Information Springer 2006
  • Publisher Name Springer, Dordrecht
  • eBook Packages Biomedical and Life Sciences
  • Print ISBN 978-1-4020-3997-3
  • Online ISBN 978-1-4020-3998-0
  • About this book