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Simple approach for the histomolecular diagnosis of central nervous system gliomas based on 2021 World Health Organization Classification
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作者 Maher Kurdi Rana H Moshref +4 位作者 Yousef Katib Eyad Faizo Ahmed A Najjar Basem Bahakeem Ahmed KBamaga 《World Journal of Clinical Oncology》 CAS 2022年第7期567-576,共10页
The classification of central nervous system(CNS)glioma went through a sequence of developments,between 2006 and 2021,started with only histological approach then has been aided with a major emphasis on molecular sign... The classification of central nervous system(CNS)glioma went through a sequence of developments,between 2006 and 2021,started with only histological approach then has been aided with a major emphasis on molecular signatures in the 4^(th) and 5^(th) editions of the World Health Organization(WHO).The recent reformation in the 5th edition of the WHO classification has focused more on the molecularly defined entities with better characterized natural histories as well as new tumor types and subtypes in the adult and pediatric populations.These new subclassified entities have been incorporated in the 5^(th) edition after the continuous exploration of new genomic,epigenomic and transcriptomic discovery.Indeed,the current guidelines of 2021 WHO classification of CNS tumors and European Association of Neuro-Oncology(EANO)exploited the molecular signatures in the diagnostic approach of CNS gliomas.Our current review presents a practical diagnostic approach for diffuse CNS gliomas and circumscribed astrocytomas using histomolecular criteria adopted by the recent WHO classification.We also describe the treatment strategies for these tumors based on EANO guidelines. 展开更多
关键词 central nervous system glioma classification world health organization 2021 European Association of Neuro-Oncology guidelines
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Pathologic research update of colorectal neuroendocrine tumors 被引量:5
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作者 Ni, Shu-Juan Sheng, Wei-Qi Du, Xiang 《World Journal of Gastroenterology》 SCIE CAS CSCD 2010年第14期1713-1719,共7页
Colorectal neuroendocrine tumors (NETs) originate from neuroendocrine cells in the intestinal tract, and represent a small area within oncology, but one which has provided increasing new data during the past years. Al... Colorectal neuroendocrine tumors (NETs) originate from neuroendocrine cells in the intestinal tract, and represent a small area within oncology, but one which has provided increasing new data during the past years. Although the World Health Organization has determined clinical and histological features to predict prognosis for such tumors, they may not be valid on an individual basis. We aim to give an overview of the recent findings with regard to pathology, molecular genetics and diagnosis of NETs. 展开更多
关键词 Neuroendocrine tumors CARCINOID COLORECTAL world health organization classification Tumornode-metastases
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Epidemiological characteristics of central nervous system tumors in children: a 5-year review of 3180 cases from Beijing Tiantan Hospital
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作者 Zhi-ming Liu Chih-yi Liao +8 位作者 Heng Zhang Zhe Han Jun-mei Wang Zhen-yu Ma Chun-de Li Jian Gong Wei Liu Tao Sun Yong-ji Tian 《Chinese Neurosurgical Journal》 CSCD 2022年第3期188-194,共7页
Background:To describe the epidemiological characteristics of central nervous system(CNS)tumors in children,based on the neurosurgery department of Beijing Tiantan Hospital.Methods:From January 2015 to December 2019,3... Background:To describe the epidemiological characteristics of central nervous system(CNS)tumors in children,based on the neurosurgery department of Beijing Tiantan Hospital.Methods:From January 2015 to December 2019,3180 children were histopathologically diagnosed with CNS tumors based on the 2016 World Health Organization(WHO)classification of tumors.Patients were 0 to 15 years old.We analyzed age-related gender preferences,tumor locations,and the histological grades of the tumors.In addition,the epidemiological characteristics of the five most common intracranial tumors were compared to the previous studies.Results:In this study,intracranial and spinal tumors account for 96.4%(3066)and 3.6%(114)of all tumors,with a preponderance of supratentorial tumors(57.9%).Among all pediatric patients,low-grade tumors comprise 67.1%(2135).The integral gender ratio of males to females is 1.47:1 and the average age of patients is 7.59 years old.The five most common intracranial tumors are craniopharyngioma(15.4%),medulloblastoma(14.3%),pilocytic astrocytoma(11.8%),diffuse astrocytoma(9.8%),and anaplastic ependymoma(4.8%).Conclusions:Due to the lack of national data on childhood brain tumors,we used a large nationally representative population sample based on the largest pediatric neurosurgery center in China.We analyzed the data of the past 5 years,reflecting the incidence of CNS tumors in Chinese children to a certain extent,and laying a data foundation for subsequent clinical studies. 展开更多
关键词 EPIDEMIOLOGY central nervous system tumors PEDIATRIC world health organization classification
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世界卫生组织中枢神经系统肿瘤分类和Ki-67指数对脑胶质瘤患者预后的影响
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作者 马林岑 杨操 +1 位作者 葛畅 徐敬轩 《中外医药研究》 2024年第6期75-77,共3页
目的:探讨世界卫生组织中枢神经系统肿瘤分类(简称WHO分级)和Ki-67指数对脑胶质瘤患者预后的影响。方法:选取2019年1月—2022年6月于新疆医科大学第二附属医院神经外科行颅内肿瘤切除术的脑胶质瘤患者22例作为研究对象。收集患者临床资... 目的:探讨世界卫生组织中枢神经系统肿瘤分类(简称WHO分级)和Ki-67指数对脑胶质瘤患者预后的影响。方法:选取2019年1月—2022年6月于新疆医科大学第二附属医院神经外科行颅内肿瘤切除术的脑胶质瘤患者22例作为研究对象。收集患者临床资料,检测病理组织Ki-67水平,根据患者是否复发或死亡分为未复发组与复发或死亡组,分析脑胶质瘤预后的影响因素,WHO分级和Ki-67指数与生存时间的关系。结果:无复发组WHO分级低分级、Ki-67指数<5%占比高于复发或死亡组,差异有统计学意义(P<0.05)。Spearman相关分析显示,胶质瘤WHO分级、Ki-67指数均与生存时间呈负相关(P<0.05)。WHO分级与Ki-67指数呈正相关(P<0.001)。结论:WHO高级别和Ki-67指数≥5%与胶质瘤患者不良预后相关。 展开更多
关键词 脑胶质瘤 世界卫生组织中枢神经系统肿瘤分类 KI-67指数 生存时间
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Efficacy of endoscopic ultrasonography-guided fine needle aspiration for pancreatic neuroendocrine tumor grading 被引量:6
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作者 Mitsuru Sugimoto Tadayuki Takagi +11 位作者 Takuto Hikichi Rei Suzuki Ko Watanabe Jun Nakamura Hitomi Kikuchi Naoki Konno Yuichi Waragai Hiroyuki Asama Mika Takasumi Hiroshi Watanabe Katsutoshi Obara Hiromasa Ohira 《World Journal of Gastroenterology》 SCIE CAS 2015年第26期8118-8124,共7页
AIM: To evaluate the efficacy of endoscopic ultrasonography-guided fine needle aspiration(EUS-FNA) for grading pancreatic neuroendocrine tumors(PNETs).METHODS: A total of 22 patients were diagnosed with PNET by EUS-FN... AIM: To evaluate the efficacy of endoscopic ultrasonography-guided fine needle aspiration(EUS-FNA) for grading pancreatic neuroendocrine tumors(PNETs).METHODS: A total of 22 patients were diagnosed with PNET by EUS-FNA between October 2001 and December 2013 at Fukushima Medical University Hospital.Among these cases,we targeted 10 PNET patients who were evaluated according to the World Health Organization(WHO) 2010 classification.Surgery was performed in eight patients,and chemotherapy was performed in two patients due to multiple liver metastases.Specimens obtained by EUS-FNA were first stained with hematoxylin and eosin and then stained with chromogranin,synaptophysin,CD56,and Ki-67.The specimens were graded by the Ki-67 index according to the WHO 2010 classification.Specimens obtained by surgery were graded by the Ki-67 indexand mitotic count(WHO 2010 classification).For the eight specimens obtained by EUS-FNA,the Ki-67 index results were compared with those obtained by surgery.In the two cases treated with chemotherapy,the effects and prognoses were evaluated.RESULTS: The sampling rate for histological diagnosis by EUS-FNA was 100%.No adverse effects were observed.The concordance rate between specimens obtained by EUS-FNA and surgery was 87.5%(7/8).Fo r t h e t w o c a s e s t re a t e d w i t h c h e m o t h e ra p y,case 1 received somatostatin analog therapy and transcatheter arterial infusion(TAI) targeting multiple liver metastases.Subsequent treatment consisted of everolimus.During chemotherapy,the primary tumor remained unconfirmed,although the multiple liver metastases diminished dramatically.Case 2 was classified as neuroendocrine carcinoma(NEC) according to the Ki-67 index of a specimen obtained by EUS-FNA; therefore,cisplatin and irinotecan therapy was started.However,severe adverse effects,including renal failure and diarrhea,were observed,and the therapy regimen was changed to cisplatin and etoposide.TAI targeting multiple liver metastases was performed.Although the liver metastases diminished,the primary tumor remained unconfirmed.These chemotherapy regimens had immediate effects for both unresectable neuroendocrine tumor(NET) and NEC cases.These two subjects are still alive.CONCLUSION: EUS-FNA was effective for PNET diagnosis and Ki-67 index grading for WHO 2010 classification,enabling informed decisions on unresectable PNET treatment by identifying NET or NEC. 展开更多
关键词 PANCREATIC NEUROENDOCRINE tumor Endoscopicultrasonography-guided fine NEEDLE ASPIRATION Ki-67index world health organization classification 2010 Chemotherapy
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2022年世界卫生组织指南头颈部肿瘤分类的解读:牙源性和颌面部骨肿瘤
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作者 张超颖 李怡宁 +1 位作者 龚佳幸 王慧明 《国际口腔医学杂志》 CAS CSCD 2023年第3期263-271,共9页
世界卫生组织出版的《头颈部肿瘤分类》是口腔颌面外科、口腔病理科医生权威的参考资料。随着近年来分子生物学的飞速发展和诊疗技术的不断提升,作为头颈部肿瘤中一类重要疾病——牙源性和颌面骨肿瘤,它在已经出版的2022年第5版中出现... 世界卫生组织出版的《头颈部肿瘤分类》是口腔颌面外科、口腔病理科医生权威的参考资料。随着近年来分子生物学的飞速发展和诊疗技术的不断提升,作为头颈部肿瘤中一类重要疾病——牙源性和颌面骨肿瘤,它在已经出版的2022年第5版中出现了许多新变化。本文主要与2017年第4版的指南比较,重点阐述了第5版在新分类、新病种和新遗传分子学改变这三方面的内容,以期辅助临床诊疗。 展开更多
关键词 牙源性肿瘤 颌面骨肿瘤 肿瘤分类 世界卫生组织
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5540例中枢神经系统肿瘤WHO分类统计分析 被引量:4
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作者 崔世民 秦进喜 +4 位作者 刘梅丽 靳松 韩彤 阎世鑫 刘力 《中国现代神经疾病杂志》 CAS 2009年第1期65-69,共5页
目的根据2007年WHO中枢神经系统肿瘤分类标准,对中枢神经系统肿瘤患者的临床资料进行统计分析,以为学术交流提供可资参考的数据。方法应用2007年WHO中枢神经系统肿瘤分类标准,对1988年7月-2008年6月经病理明确诊断的5540例中枢神经... 目的根据2007年WHO中枢神经系统肿瘤分类标准,对中枢神经系统肿瘤患者的临床资料进行统计分析,以为学术交流提供可资参考的数据。方法应用2007年WHO中枢神经系统肿瘤分类标准,对1988年7月-2008年6月经病理明确诊断的5540例中枢神经系统肿瘤患者的性别、年龄及肿瘤类型、级别进行分析,并与相关文献进行比较。结果神经上皮组织肿瘤2205例,占39.80%;脑神经和脊旁神经肿瘤361例,占6.52%;脑膜肿瘤2105例,占38.00%;淋巴和造血组织肿瘤91例,占1.64%;生殖细胞肿瘤86例,占1.55%;蝶鞍区肿瘤(颅咽管瘤)250例,占4.51%;转移性肿瘤442例,占7.98%;儿童中枢神经系统肿瘤449例,占8.10%。结论2007年WHO中枢神经系统肿瘤分类标准对统一中枢神经系统肿瘤的命名与分类、了解不同地区肿瘤分布特征、进行流行病学调查及学术交流十分必要。 展开更多
关键词 中枢神经系统肿瘤 国际疾病分类法 世界卫生组织
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137例胸腺上皮肿瘤的预后影响因素 被引量:4
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作者 陈晨 尹邦良 +4 位作者 魏启幼 胡建国 喻风雷 袁运长 赵元 《中南大学学报(医学版)》 CAS CSCD 北大核心 2009年第4期340-344,共5页
目的:通过对胸腺上皮肿瘤患者临床、病理资料进行分析,探寻与疾病预后相关的影响因素。方法:本院心胸外科1997年6月至2007年9月胸腺上皮肿瘤病例137例,记录患者临床、病理资料,并于术后进行随访,按照Masaoka病理分期将所有病例分为Masao... 目的:通过对胸腺上皮肿瘤患者临床、病理资料进行分析,探寻与疾病预后相关的影响因素。方法:本院心胸外科1997年6月至2007年9月胸腺上皮肿瘤病例137例,记录患者临床、病理资料,并于术后进行随访,按照Masaoka病理分期将所有病例分为MasaokaI/Ⅱ期和Ⅲ/Ⅳ期两组,按照WHO组织学分型将所有病例分为WHOA/AB/B1组和B2/B3/C组,应用Kaplan-Meier法、COX回归模型等寻找疾病预后的相关因素。结果:所有病例中124例(90.5%)行全切手术,9例(6.6%)行姑息性切除,4例(2.9%)行活检术。MasaokaⅠ/Ⅱ期病例中手术全切率(100%)明显高于Ⅲ/Ⅳ期病例的全切率(分别为67.9%和63.6%,P<0.001)。137例病例中总的5年、10年总生存率为71.4%和50.1%。MasaokaI/Ⅱ期病例生存率明显高于Ⅲ期、Ⅳ期病例(P<0.001);按照WHO分型,A/AB/B1型5年、10年生存率明显高于B2/B3/C型病例(P<0.001);完全切除病例术后5年、10年生存率明显高于不完全切除和活检病例(P<0.001)。COX回归分析发现,Masaoka病理分期、WHO组织学分型、肿瘤完全切除及手术时年龄与预后相关。结论:Masaoka病理分期、WHO组织学分型、肿瘤完全切除及手术时患者年龄是胸腺上皮肿瘤患者重要的预后相关因素。 展开更多
关键词 胸腺上皮肿瘤 Masaoka病理分期 WHO组织学分型 预后
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2017版WHO牙源性肿瘤新分类之述评 被引量:15
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作者 陶谦 梁培盛 《口腔疾病防治》 2017年第12期749-754,共6页
第四版《WHO头颈部肿瘤分类》于2017年1月出版,该书第8章重点介绍了牙源性及颌面骨肿瘤的新分类。与2005版(第三版)分类相比,2017版新分类牙源性肿瘤部分发生了较大幅度的变动。本文重点介绍2017版牙源性肿瘤分类的新变化并对新分类的... 第四版《WHO头颈部肿瘤分类》于2017年1月出版,该书第8章重点介绍了牙源性及颌面骨肿瘤的新分类。与2005版(第三版)分类相比,2017版新分类牙源性肿瘤部分发生了较大幅度的变动。本文重点介绍2017版牙源性肿瘤分类的新变化并对新分类的修订内容作一简要述评。 展开更多
关键词 肿瘤分类 牙源性肿瘤 牙源性囊肿 病理学 分子遗传学 世界卫生组织
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2007年WHO神经系统肿瘤分类(第四版)几个新增肿瘤类型 被引量:10
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作者 何妙侠 王建军 《中国神经肿瘤杂志》 2007年第4期286-290,共5页
2007年新修改的WHO关于神经系统肿瘤分类(第4版)共增加了七种新的肿瘤类型,包括血管中心性胶质瘤、毛细胞粘液样星形细胞瘤、垂体细胞瘤、乳头状胶质神经元肿瘤、第四脑室菊形团形成的胶质神经元肿瘤,松果体区乳头状肿瘤和腺垂体梭形细... 2007年新修改的WHO关于神经系统肿瘤分类(第4版)共增加了七种新的肿瘤类型,包括血管中心性胶质瘤、毛细胞粘液样星形细胞瘤、垂体细胞瘤、乳头状胶质神经元肿瘤、第四脑室菊形团形成的胶质神经元肿瘤,松果体区乳头状肿瘤和腺垂体梭形细胞嗜酸细胞瘤,学习和掌握这些肿瘤的临床、形态、免疫和遗传学特点,对作好神经系统肿瘤的临床与病理诊断大有裨益。 展开更多
关键词 神经系统肿瘤 WHO分类 新类型
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中枢神经系统肿瘤的临床调查与分析 被引量:6
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作者 陆坤 顾培元 +4 位作者 魏栋 陈功 缪宗 胡士伟 胡卫星 《临床神经外科杂志》 CAS 2018年第4期296-300,共5页
目的研究江苏省人民医院近10年来中枢神经系统肿瘤的流行病学特点。方法统计分析江苏省人民医院近10年来,经手术治疗并取得病理学诊断的4553例中枢神经系统肿瘤患者的临床资料。结果按WHO 2016年新分类标准分型,本组患者以脑膜瘤(28.05%... 目的研究江苏省人民医院近10年来中枢神经系统肿瘤的流行病学特点。方法统计分析江苏省人民医院近10年来,经手术治疗并取得病理学诊断的4553例中枢神经系统肿瘤患者的临床资料。结果按WHO 2016年新分类标准分型,本组患者以脑膜瘤(28.05%)、鞍区肿瘤(25.98%)、弥漫性星形细胞和少突胶质细胞肿瘤(18.52%)、椎管内神经肿瘤(13.33%)、间质,非脑膜上皮性肿瘤(6.35%)为主。低级别肿瘤占86.43%,幕上肿瘤占71.47%,男女性别比为1∶1.32,发病率峰值为50~59岁。结论中枢神经系统肿瘤的临床特征与患者来源区域的地理环境、产业结构、经济发展、化工污染、人口性别比、医疗条件,以及患者职业等有着紧密联系。 展开更多
关键词 中枢神经系统肿瘤 临床调查 WHO分类 流行病学
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Pancreatic neuroendocrine neoplasms: Magnetic resonance imaging features according to grade and stage 被引量:17
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作者 Riccardo De Robertis Sara Cingarlini +11 位作者 Paolo Tinazzi Martini Silvia Ortolani Giovanni Butturini Luca Landoni Paolo Regi Roberto Girelli Paola Capelli Stefano Gobbo Giampaolo Tortora Aldo Scarpa Paolo Pederzoli Mirko D'Onofrio 《World Journal of Gastroenterology》 SCIE CAS 2017年第2期275-285,共11页
AIM To describe magnetic resonance(MR) imaging features of pancreatic neuroendocrine neoplasms(Pan NENs) according to their grade and tumor-nodes-metastases stage by comparing them to histopathology and todetermine th... AIM To describe magnetic resonance(MR) imaging features of pancreatic neuroendocrine neoplasms(Pan NENs) according to their grade and tumor-nodes-metastases stage by comparing them to histopathology and todetermine the accuracy of MR imaging features in predicting their biological behavior.METHODS This study was approved by our institutional review board; requirement for informed patient consent was waived due to the retrospective nature of the study. Preoperative MR examinations of 55 Pan NEN patients(29 men, 26 women; mean age of 57.6 years, range 21-83 years) performed between June 2013 and December 2015 were reviewed. Qualitative and quantitative features were compared between tumor grades and stages determined by histopathological analysis.RESULTS Ill defined margins were more common in G2-3 and stage Ⅲ-Ⅳ PanN ENs than in G1 and low-stage tumors(P < 0.001); this feature had high specificity in the identification of G2-3 and stage Ⅲ-Ⅳ tumors(90.3% and 96%, 95%CI: 73.1-97.5 and 77.7-99.8). The mean apparent diffusion coefficient value was significantly lower in G2-3 and stage Ⅲ-Ⅳ lesions compared to well differentiated and low-stage tumors(1.09 × 10-3 mm2/s vs 1.45 × 10-3 mm2/s and 1.10 × 10-3 mm2/s vs 1.53 × 10-3 mm2/s, P = 0.003 and 0.001). Receiving operator characteristic analysis determined optimal cutoffs of 1.21 and 1.28 × 10-3 mm2/s for the identification of G2-3 and stage Ⅲ-Ⅳ tumors, with sensitivity and specificity values of 70.8/80.7% and 64.5/64%(95%CI: 48.7-86.6/60-92.7 and 45.4-80.2/42.6-81.3).CONCLUSION MR features of PanN ENs vary according to their grade of differentiation and their stage at diagnosis and could predict the biological behavior of these tumors. 展开更多
关键词 胰腺的 neuroendocrine 肿瘤 世界健康组织分类 2010 散开加权的成像 欧洲 Neuroendocrine 肿瘤社会阶段系统 磁性的回声成像
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Expression and prognostic value of brain and acute leukemia,cytoplasmic in meningiomas
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作者 Yong-Tao He Qiao Zhou +3 位作者 Tao Zhu Jia Zhu Jing Zhang Mei Jin 《Chinese Medical Journal》 SCIE CAS CSCD 2019年第18期2248-2250,共3页
To the Editor:Meningiomas are the most common central nervous system neoplasms.[1] The World Health Organization (WHO) 2016 classification system classifies meningiomas into three grades:grade Ⅰ (benign),grade Ⅱ (at... To the Editor:Meningiomas are the most common central nervous system neoplasms.[1] The World Health Organization (WHO) 2016 classification system classifies meningiomas into three grades:grade Ⅰ (benign),grade Ⅱ (atypical),and grade Ⅲ (anaplastic/malignant) meningioma.[1] Benign meningiomas are usually associated with favorable prognosis;however,higher grade (WHO grades Ⅱ and Ⅲ) menigiomas are more aggressive,resulting in less favorable outcome. 展开更多
关键词 central nervous system world health organization MENINGIOMA
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2016年WHO中枢神经系统肿瘤分类解读 被引量:19
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作者 魏社鹏 赵继宗 《中华神经医学杂志》 CSCD 北大核心 2017年第5期529-536,共8页
2016年WHO中枢神经系统(CNS)肿瘤分类(简称2016分类)首次采用分子参数(不仅仅是组织学参数)定义了许多肿瘤实体,因而明确的阐述了一个概念,即在分子时代CNS肿瘤的诊断应当如何构建。依此,2016分类提出了主要针对弥漫性胶质瘤... 2016年WHO中枢神经系统(CNS)肿瘤分类(简称2016分类)首次采用分子参数(不仅仅是组织学参数)定义了许多肿瘤实体,因而明确的阐述了一个概念,即在分子时代CNS肿瘤的诊断应当如何构建。依此,2016分类提出了主要针对弥漫性胶质瘤、髓母细胞瘤和其他胚胎性肿瘤的重新分组,同时增加了被组织和分子特点所定义的新实体,包括胶质母细胞瘤(异柠檬酸脱氢酶(IDH)-野生型)和胶质母细胞瘤(IDn.突变型)、弥漫性中线胶质瘤(H3K4M-突变型)、室管膜瘤(RELA融合-阳性)、髓母细胞瘤(WNT激活的)、髓母细胞瘤(SHH激活的)和胚胎性肿瘤伴多层菊形团(C19MC-改变的)。总之,2016分类增加了新确定的肿瘤,丢弃了一些不再具有诊断相关性和(或)生物相关性的实体、变种和雏型。2016分类能够让临床诊疗、临床试验和流行病学研究变得更加便利.从而有利于改善CNS肿瘤患者的生活质量。 展开更多
关键词 中枢神经系统 肿瘤分类 世界卫生组织
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2022版世界卫生组织垂体神经内分泌肿瘤的病理新分类和临床启示 被引量:1
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作者 谢静 吴哲褒 《中华医学杂志》 CAS CSCD 北大核心 2022年第47期3723-3726,共4页
2022年世界卫生组织对垂体腺瘤再次提出新分类,其命名正式进入垂体神经内分泌肿瘤(PitNETs)的时代。新分类中,常规使用垂体转录因子(PIT1、TPIT、SF1、GATA3和ERα)和激素等抗体提供了PitNETs的详细组织学亚型。PIT1、TPIT和SF1谱系定义... 2022年世界卫生组织对垂体腺瘤再次提出新分类,其命名正式进入垂体神经内分泌肿瘤(PitNETs)的时代。新分类中,常规使用垂体转录因子(PIT1、TPIT、SF1、GATA3和ERα)和激素等抗体提供了PitNETs的详细组织学亚型。PIT1、TPIT和SF1谱系定义的PitNETs类型和亚型具有明显的形态学、分子和临床差异。与2017版相比,主要改变包括:(1)嗜酸细胞干细胞型和泌乳素生长激素细胞瘤、混合性泌乳-生长激素细胞腺瘤,在2022版中均作为一个独立的类型;(2)未成熟PIT1谱系肿瘤和成熟多激素PIT1谱系肿瘤,取代原先的多激素PIT1阳性腺瘤;(3)提倡用"转移性PitNET"来取代之前的"垂体癌"。新版分类强调了PitNETs病理分型的重要性,很显然,准确的病理解读是判断临床治疗路径和预后的关键。 展开更多
关键词 世界卫生组织 垂体神经内分泌肿瘤 垂体腺瘤 肿瘤细胞谱系 肿瘤分类
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