Prajapati Hanuman Prasad, Kannaujia Sanjay Kumar
Department of Neurosurgery, Uttar Pradesh University of Medical Sciences, Etawah, Uttar Pradesh, India.
Department of Pathology, Uttar Pradesh University of Medical Sciences, Etawah, Uttar Pradesh, India.
Surg Neurol Int. 2022 Jun 17;13:252. doi: 10.25259/SNI_102_2022. eCollection 2022.
Building on the 2016 updated fourth edition and the work of consortium to inform molecular and practical approach to CNS tumor taxonomy, the major dramatic change occurs in 2021 fifth edition by advancing the role of molecular diagnostics in CNS tumor classification. The present review summarizes the major general changes in the 2021 fifth edition classification and the specific changes in each taxonomic category.
The review was designed in accordance to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis. Articles published in PubMed Central, Medline, and Embase databases till now were all searched. Only nonexperimental and nonanimal clinical studies were included in the study. Articles written only in the English language were considered.
All IDH mutant diffuse astrocytic tumors are considered in a single type "astrocytoma IDH mutant" and then graded as CNS WHO Grades 2-4. Pediatric-type diffuse gliomas are now classified as separate entity. Anatomical site is also taken into consideration to classify ependymoma. The "Desmoplastic myxoid tumor of the pineal region, SMARCB1 mutant" and "Atypical neurofibromatous neoplasm of unknown biological potential" are new tumor type added to pineal and neurofibroma group, respectively. Mesenchymal tumor is now termed as only solitary fibrous tumor. Adamantinomatous and papillary subtype of craniopharyngioma are now classified as distinct tumor type. The new term "Pituitary neuroendocrine tumor" has been coined for pituitary adenoma.
The WHO CNS-5 introduces a new knowledge into the classification with progressive manner by introducing newly recognizing entities, by obsoleting tumor type, and by adjusting the taxonomic structure.
基于2016年更新的第四版以及相关联盟的工作,以提供中枢神经系统肿瘤分类的分子和实用方法,2021年第五版发生了重大变化,即提升了分子诊断在中枢神经系统肿瘤分类中的作用。本综述总结了2021年第五版分类中的主要总体变化以及每个分类类别的具体变化。
本综述按照系统评价和Meta分析的首选报告项目进行设计。检索了截至目前在PubMed Central、Medline和Embase数据库中发表的文章。研究仅纳入非实验性和非动物临床研究。仅考虑用英语撰写的文章。
所有异柠檬酸脱氢酶(IDH)突变型弥漫性星形细胞瘤被归为单一类型“IDH突变型星形细胞瘤”,然后分为世界卫生组织(WHO)中枢神经系统2-4级。儿童型弥漫性胶质瘤现在被分类为单独的实体。室管膜瘤的分类也考虑了解剖部位。“松果体区促纤维增生性黏液样肿瘤,SMARCB1突变型”和“生物学潜能未知的非典型神经纤维瘤性肿瘤”分别是新增到松果体和神经纤维瘤组的新肿瘤类型。间叶性肿瘤现在仅称为孤立性纤维瘤。颅咽管瘤的牙釉质型和乳头型亚型现在被分类为不同的肿瘤类型。垂体腺瘤有了新术语“垂体神经内分泌肿瘤”。
WHO中枢神经系统肿瘤分类第5版通过引入新识别的实体、淘汰肿瘤类型以及调整分类结构,以渐进的方式为分类引入了新知识。