胶质瘤的诊断和发病机制

Colin Smith, James W. Ironside
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引用次数: 22

摘要

胶质瘤是儿童和成人中枢神经系统(CNS)中最常见的肿瘤。这两个年龄组的发病率似乎都在增加,原因尚不清楚。胶质瘤的生物学行为各不相同,从生长缓慢、界限清晰、可通过切除治愈的肿瘤到恶性侵袭性肿瘤,都是致命的。病理学在胶质瘤患者的治疗中起着重要的作用,它提供了组织学诊断和肿瘤分级,这对预后具有重要意义。分子遗传学研究发现,许多神经胶质瘤中遗传物质的丢失,随着肿瘤级别的增加,遗传物质的丢失逐渐增加。在少突胶质细胞瘤中,染色体1p和19q上的杂合性缺失作为肿瘤对化疗反应的预测因子具有治疗意义。世卫组织即将修订的中枢神经系统肿瘤分类预计将提供有关胶质瘤诊断和分级的最新建议。
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Diagnosis and pathogenesis of gliomas

Gliomas are the commonest groups of tumours arising in the central nervous system (CNS) in both children and adults. Their incidence in both age groups appears to be increasing, for reasons that are poorly understood. The biological behaviour of gliomas varies from slow-growing well-demarcated tumours that are curable by excision to malignant invasive tumours that are uniformly fatal. Pathology has a major role to play in the management of patients with gliomas by providing a histological diagnosis and tumour grade, which are of major prognostic significance. Molecular genetic studies have found loss of genetic material in many gliomas, with progressive losses identified with increasing tumour grade. In oligodendrogliomas, loss of heterozygosity on chromosomes 1p and 19q is of therapeutic significance as a predictor of tumour response to chemotherapy. The forthcoming revision of the WHO classification of CNS tumours is expected to provide updated recommendations on glioma diagnosis and grading.

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