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[胶质瘤诊断和预后价值的临床病理及分子学方面]

[Clinico-pathological and molecular aspects of diagnostic and prognostic value in gliomas].

作者信息

Ortega-Aznar A, Jimenez-Leon P, Martinez E, Romero-Vidal F J

机构信息

Servicio de Anatomía Patológica, Hospital Universitario Vall d'Hebron, Barcelona, Espana.

出版信息

Rev Neurol. 2013 Feb 1;56(3):161-70.

Abstract

INTRODUCTION

Diffuse infiltrative gliomas, the most common primary brain tumours, account for almost 80% of malignant brain tumours. 60-70% of gliomas are astrocytic and over 80% of these tumours is considered high grade malignancy (grade III and IV) according to current World Health Organization classification. Infiltrating gliomas include diffuse astrocytomas, oligodendrogliomas and oligoastrocytomas.

AIM

To review the clinical and histological features of cerebral gliomas, and molecular alterations that add relevant information for novel approaches in diagnosis, prognosis and treatment.

DEVELOPMENT

The current gold standard diagnosis of these tumours relies on histopathological classification, which provides a grading of malignancy as a predictor of biological behaviour. However emerging molecular abnormalities have been discovered in the last years and these molecular changes are playing an increasingly prominent role as predictive biomarkers or in the development of diagnostic and prognostic. Now the neuropathologist is in crossroads between pathology and molecular biology and he plays a significant role in implementation of treatments and/or clinical trials.

CONCLUSIONS

The study of proteomics and molecular biomarkers should complement the histopathological analysis and sometimes allows to determine direct or indirect predictive factors as well as the study of affected pathways which may become selective therapeutic targets.

摘要

引言

弥漫性浸润性胶质瘤是最常见的原发性脑肿瘤,占恶性脑肿瘤的近80%。根据世界卫生组织目前的分类,60%-70%的胶质瘤是星形细胞性的,其中超过80%的肿瘤被认为是高级别恶性肿瘤(III级和IV级)。浸润性胶质瘤包括弥漫性星形细胞瘤、少突胶质细胞瘤和少突星形细胞瘤。

目的

回顾脑胶质瘤的临床和组织学特征,以及为诊断、预后和治疗新方法提供相关信息的分子改变。

进展

目前这些肿瘤的金标准诊断依赖于组织病理学分类,该分类提供恶性程度分级作为生物学行为的预测指标。然而,近年来发现了新出现的分子异常,这些分子变化在作为预测生物标志物或在诊断和预后发展中发挥着越来越突出的作用。现在神经病理学家正处于病理学和分子生物学的交叉点,并且在治疗实施和/或临床试验中发挥着重要作用。

结论

蛋白质组学和分子生物标志物的研究应补充组织病理学分析,有时可以确定直接或间接的预测因素以及对可能成为选择性治疗靶点的受影响途径的研究。

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