{"title":"Medulloblastoma","authors":"J. Rutka","doi":"10.1093/med/9780198746706.003.0028","DOIUrl":null,"url":null,"abstract":"Under the term embryonal tumours, we examine the malignant neoplasms medulloblastomas, CNS-PNETs, AT/RTs, and ETANTRs. The common histological link between them is the small, round, blue cells which appear on H&E stains. They are considered highly malignant tumours (WHO Grade IV), although significant variation of prognosis exists between the different subtypes. Current classification is based on their histopathological features. Advances on understanding of the molecular biology and behaviour of their cellular lines, has dramatically changed their stratification and scientific approach. Combination of surgical treatment with new schemes of adjuvant chemo- and radiotherapy offers improved survival rates but comes with a high cost on neurocognitive, endocrine, and overall functional status. New therapies with molecular targets will hopefully improve outcomes with minimal side effects and collateral damage.","PeriodicalId":115670,"journal":{"name":"Oxford Textbook of Neurological Surgery","volume":"262 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oxford Textbook of Neurological Surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/med/9780198746706.003.0028","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

Under the term embryonal tumours, we examine the malignant neoplasms medulloblastomas, CNS-PNETs, AT/RTs, and ETANTRs. The common histological link between them is the small, round, blue cells which appear on H&E stains. They are considered highly malignant tumours (WHO Grade IV), although significant variation of prognosis exists between the different subtypes. Current classification is based on their histopathological features. Advances on understanding of the molecular biology and behaviour of their cellular lines, has dramatically changed their stratification and scientific approach. Combination of surgical treatment with new schemes of adjuvant chemo- and radiotherapy offers improved survival rates but comes with a high cost on neurocognitive, endocrine, and overall functional status. New therapies with molecular targets will hopefully improve outcomes with minimal side effects and collateral damage.
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成神经管细胞瘤
在胚胎肿瘤这一术语下,我们研究了髓母细胞瘤、CNS-PNETs、AT/RTs和ETANTRs等恶性肿瘤。它们之间的共同组织学联系是H&E染色上出现的小而圆的蓝色细胞。它们被认为是高度恶性肿瘤(世卫组织四级),尽管不同亚型之间的预后存在显著差异。目前的分类是基于他们的组织病理学特征。对其细胞系的分子生物学和行为的理解的进步,极大地改变了它们的分层和科学方法。手术治疗与新的辅助化疗和放疗方案相结合可提高生存率,但在神经认知、内分泌和整体功能状态方面代价高昂。以分子为靶点的新疗法有望以最小的副作用和附带损害改善治疗效果。
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