Kleihues P, Burger P C, Scheithauer B W
Department of Pathology, University Hospital, Zurich, Switzerland.
Brain Pathol. 1993 Jul;3(3):255-68. doi: 10.1111/j.1750-3639.1993.tb00752.x.
The new edition of the World Health Organization (WHO) book on 'Histological Typing of Tumours of the Central Nervous System' reflects the progress in brain tumour classification which has been achieved since publication of the first edition in 1979. Several new tumour entities have been added, including the pleomorphic xanthoastrocytoma, central neurocytoma, the infantile desmoplastic astrocytoma/ganglioglioma, and the dysembryoplastic neuroepithelial tumour. The list of histological variants has also been expanded. In line with recent morphological and molecular data on glioma progression, the glioblastoma is now grouped together with astrocytic tumours. The classification of childhood tumours has been largely retained, the diagnosis primitive neuroectodermal tumour (PNET) only being recommended as a generic term for cerebellar medulloblastomas and neoplasms that are histologically indistinguishable from medulloblastoma but located in the CNS at sites other than the cerebellum. The WHO grading scheme was revised and adapted to new entities but its use, as before, remains optional.
世界卫生组织(WHO)关于《中枢神经系统肿瘤组织学分类》的新版书籍反映了自1979年第一版出版以来在脑肿瘤分类方面所取得的进展。新增了几种新的肿瘤实体,包括多形性黄色星形细胞瘤、中枢神经细胞瘤、婴儿促纤维增生性星形细胞瘤/节细胞胶质瘤以及胚胎发育不良性神经上皮肿瘤。组织学变异类型的列表也有所扩充。根据近期关于胶质瘤进展的形态学和分子数据,现在将胶质母细胞瘤与星形细胞肿瘤归为一类。儿童肿瘤的分类在很大程度上得以保留,仅建议将原始神经外胚层肿瘤(PNET)作为小脑髓母细胞瘤以及组织学上与髓母细胞瘤难以区分但位于中枢神经系统小脑以外部位的肿瘤的通用术语。WHO分级方案进行了修订并适用于新的实体,但与以前一样,其使用仍然是可选择的。