神经胶质肿瘤

IF 0.1 Q4 PATHOLOGY
C. Welsh
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引用次数: 2

摘要

神经胶质肿瘤占原发性轴内颅内肿瘤的大多数。世界卫生组织(WHO)中枢神经系统肿瘤分类修订第四版自2016年推出以来,改变了神经胶质肿瘤的诊断和治疗方法(WHO中枢神经系统肿瘤分类[修订第四版];里昂,法国:国际癌症研究机构;2016)。弥漫性胶质瘤(WHO分级II-IV级)现在根据异柠檬酸脱氢酶1或2突变状态进行分子分层,并根据1p/19q编码状态分为星形细胞型或少突胶质型。现在更新的速度比世卫组织新版本的分类编制速度要快,因此更新是通过CNS肿瘤分类分子和实用方法通报联盟的期刊文章发布的(Brain Pathol 2019;29(4): 469-472)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Glial Tumors
Abstract Glial tumors comprise the majority of primary intra-axial intracranial tumors. Since its introduction in 2016, the revised fourth edition of the World Health Organization (WHO) classification of central nervous system tumors has changed the diagnostic and therapeutic approach in glial tumors (WHO Classification of Tumours of the Central Nervous System [revised fourth edition]; Lyon, France: IARC; 2016). Diffuse gliomas (WHO grades II–IV) are now molecularly stratified based on isocitrate dehydrogenase 1 or 2 mutation status and classified according to 1p/19q codeletion status into astrocytic or oligodendroglial type. Updates now occur faster than new editions of the WHO classification can be prepared, so updates are being issued by way of journal articles from a Consortium to Inform Molecular and Practical Approaches to CNS Tumor Taxonomy (Brain Pathol 2019;29(4):469–472).
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来源期刊
CiteScore
0.30
自引率
0.00%
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