Kleihues Paul, Louis David N, Scheithauer Bernd W, Rorke Lucy B, Reifenberger Guido, Burger Peter C, Cavenee Webster K
International Agency for Research on Cancer (IARC), Lyon, France.
J Neuropathol Exp Neurol. 2002 Mar;61(3):215-25; discussion 226-9. doi: 10.1093/jnen/61.3.215.
The new World Health Organization (WHO) classification of nervous system tumors, published in 2000, emerged from a 1999 international consensus conference of neuropathologists. New entities include chordoid glioma of the third ventricle, cerebellar liponeurocytoma, atypical teratoid/rhabdoid tumor, and perineurioma. Several histological variants were added, including tanycytic ependymoma, large cell medulloblastoma, and rhabdoid meningioma. The WHO grading scheme was updated and, for meningiomas, extensively revised. In recognition of the emerging role of molecular diagnostic approaches to tumor classification, genetic profiles have been emphasized, as in the distinct subtypes of glioblastoma and the already clinically useful 1p and 19q markers for oligodendroglioma and 22q/INI1 for atypical teratoid/rhabdoid tumors. In accord with the new WHO Blue Book series, the actual classification is accompanied by extensive descriptions and illustrations of clinicopathological characteristics of each tumor type, including molecular genetic features, predictive factors, and separate chapters on inherited tumor syndromes. The 2000 WHO classification of nervous system tumors aims at being used and implemented by the neuro-oncology and biomedical research communities worldwide.
2000年出版的世界卫生组织(WHO)新版神经系统肿瘤分类,源自1999年神经病理学家国际共识会议。新的肿瘤类型包括第三脑室脊索样胶质瘤、小脑脂肪神经细胞瘤、非典型畸胎样/横纹肌样瘤和神经束膜瘤。增加了几种组织学变异型,包括伸长细胞型室管膜瘤、大细胞型髓母细胞瘤和横纹肌样脑膜瘤。WHO分级方案进行了更新,对于脑膜瘤分级进行了广泛修订。鉴于分子诊断方法在肿瘤分类中日益重要的作用,强调了基因特征,如胶质母细胞瘤的不同亚型以及少突胶质细胞瘤中已具有临床应用价值的1p和19q标记,非典型畸胎样/横纹肌样瘤中的22q/INI1标记。按照WHO新蓝皮书系列,实际分类伴有每种肿瘤类型临床病理特征的详尽描述和图示,包括分子遗传学特征、预测因素以及关于遗传性肿瘤综合征的单独章节。2000年WHO神经系统肿瘤分类旨在供全球神经肿瘤学和生物医学研究领域使用和实施。