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| 008 | 100301s2006 ne | s |||| 0|eng d | ||
| 020 | _a9781402039980 | ||
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_aRD663 _b.S354 2006 EB |
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| 082 | 0 | 4 | _a614.5999 |
| 100 | 1 |
_aSchiffer, Davide _984284 _0Local |
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| 245 | 1 | 0 |
_aBrain Tumor Pathology : _bCurrent Diagnostic Hotspots and Pitfalls _cby Davide Schiffer |
| 260 |
_aDordrecht _bSpringer International Publishing _c2006 |
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| 300 | _a1 recurso en línea (VI, 272 p.) | ||
| 336 |
_aTexto (visual) _btxt _2rdacontent |
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| 337 |
_aelectrónico _bc _2rdamedia |
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_arecurso electrónico _bcr _2rdacarrier |
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_aonline resource _bcr _2rdacarrier |
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| 520 | _aSince 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. | ||
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| 988 | _aEBOOK, EBSPRINGERrevisado | ||
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_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://link.springer.com/book/10.1007/1-4020-3998-0 _zAcceso a este recurso digital (usuarios Universidad Europea de Madrid) |
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