Record Display for the EPA National Library Catalog

RECORD NUMBER: 35 OF 349

OLS Field Name OLS Field Data
Main Title Brain Tumor Pathology: Current Diagnostic Hotspots and Pitfalls [electronic resource] /
Type EBOOK
Author Schiffer, Davide.
Publisher Springer Netherlands,
Year Published 2006
Call Number RC261-271
ISBN 9781402039980
Subjects Medicine. ; Oncology. ; Neurosciences. ; Neurology. ; Neurosurgery. ; Pathology.
Internet Access
Description Access URL
http://dx.doi.org/10.1007/1-4020-3998-0
Collation VI, 272 p. online resource.
Notes
Due to license restrictions, this resource is available to EPA employees and authorized contractors only
Contents Notes
The Origin of Gliomas in Relation to the Histological Diagnosis -- Molecular Genetics Outline of Brain Tumors -- General Remarks -- Astrocytic Tumors I -- Astrocytic Tumors II -- Oligodendroglial Tumors -- Ependymal Tumors -- Neuronal and Mixed Glio-Neural Tumors I -- Neuronal and Mixed Glio-Neural Tumors II -- Peculiar Tumors -- Cell Migration and Invasion -- Apoptosis -- The Ubiquitin-Proteasome System -- Angiogenesis -- Meningiomas. 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.