• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

胶质肉瘤:神经影像学和免疫组织化学表现。

Gliosarcoma: Neuroimaging and Immunohistochemical Findings.

机构信息

Department of Radiology and Imaging Sciences, University of Utah Health Sciences Center, Salt Lake City, UT.

Department of Pathology, University of Utah Health Sciences Center, Salt Lake City, UT.

出版信息

J Neuroimaging. 2019 Jan;29(1):126-132. doi: 10.1111/jon.12565. Epub 2018 Oct 8.

DOI:10.1111/jon.12565
PMID:30295979
Abstract

BACKGROUND AND PURPOSE

Gliosarcoma (GSC) is an intra-axial lesion which often abuts a dural margin and is composed of glial and mesenchymal elements. This lesion is considered a variant of isocitrate dehydrogenase (IDH)-wild type glioblastoma (GBM). The purpose of this study is to evaluate the imaging and molecular features of GSC in a large patient cohort.

METHODS

Pathology-proved GSC cases were collected from our quaternary care center spanning the last 16 years and IDH status was documented. Older GSC cases without prior immunohistochemical testing underwent tissue block staining to obtain IDH status. When available, p53, phosphate and tensin (PTEN), MIB-1, EGFR amplification, and MGMT methylation were recorded and imaging findings tabulated. Logistic regression analyses were performed to determine correlation of molecular markers and imaging characteristics.

RESULTS

A total of 25 cases were identified (21 de novo, 4 post-treatment). All lesions contacted a dural, pial, or ependymal surface and were negative for an IDH R132H mutation, including postradiation GSC. In total, 16 of 16 cases showed nonamplification of EGFR/CEP7, 2 of 16 demonstrated MGMT methylation, and multiple lesions demonstrated p53 and PTEN mutations. Imaging features included areas of nodular thickening in necrotic lesions which appeared to abut the site of dural contact. There was no significant correlation of molecular markers with imaging characteristics.

CONCLUSION

GSC was IDH(-) in all cases, supporting the current understanding of this lesion being a wild-type GBM variant. Additional molecular markers demonstrated no significant correlation with imaging findings in this cohort.

摘要

背景与目的

神经胶母肉瘤(gliosarcoma,GSC)是一种位于脑内的病变,常与硬脑膜边缘相邻,由神经胶质和间叶成分组成。该病变被认为是异柠檬酸脱氢酶(IDH)野生型胶质母细胞瘤(glioblastoma,GBM)的一种变体。本研究的目的是在一个大型患者队列中评估 GSC 的影像学和分子特征。

方法

从我们的四级医疗中心收集了过去 16 年中经病理证实的 GSC 病例,并记录了 IDH 状态。对于没有先前免疫组织化学检测的较老的 GSC 病例,进行组织块染色以获得 IDH 状态。当有条件时,记录 p53、磷酸和张力蛋白(phosphate and tensin,PTEN)、MIB-1、表皮生长因子受体(epidermal growth factor receptor,EGFR)扩增和 O6-甲基鸟嘌呤-DNA 甲基转移酶(O6-methylguanine-DNA methyltransferase,MGMT)甲基化,并列出影像学表现。进行逻辑回归分析以确定分子标志物和影像学特征的相关性。

结果

共确定了 25 例病例(21 例为初发,4 例为治疗后)。所有病变均与硬脑膜、软脑膜或室管膜表面接触,且 IDH R132H 突变均为阴性,包括放疗后 GSC。16 例中有 16 例 EGFR/CEP7 无扩增,2 例有 MGMT 甲基化,多个病变有 p53 和 PTEN 突变。影像学特征包括坏死病变中出现结节性增厚区,这些区域似乎与硬脑膜接触部位相邻。在本队列中,分子标志物与影像学特征之间没有显著相关性。

结论

所有病例的 GSC 均为 IDH(-),支持目前对该病变为野生型 GBM 变体的认识。在本队列中,其他分子标志物与影像学发现之间没有显著相关性。

相似文献

1
Gliosarcoma: Neuroimaging and Immunohistochemical Findings.胶质肉瘤:神经影像学和免疫组织化学表现。
J Neuroimaging. 2019 Jan;29(1):126-132. doi: 10.1111/jon.12565. Epub 2018 Oct 8.
2
Primary and secondary gliosarcomas: clinical, molecular and survival characteristics.原发性和继发性胶质肉瘤:临床、分子及生存特征
J Neurooncol. 2015 Nov;125(2):401-10. doi: 10.1007/s11060-015-1930-y. Epub 2015 Sep 9.
3
An IDH1-mutated primary gliosarcoma: case report.伴 IDH1 突变的原发性胶质肉瘤:病例报告。
J Neurosurg. 2017 Feb;126(2):476-480. doi: 10.3171/2016.2.JNS151482. Epub 2016 May 6.
4
Clinical insights gained by refining the 2016 WHO classification of diffuse gliomas with: EGFR amplification, TERT mutations, PTEN deletion and MGMT methylation.通过对 2016 年 WHO 弥漫性胶质瘤分类进行以下四项指标的细化:EGFR 扩增、TERT 突变、PTEN 缺失和 MGMT 甲基化,获得的临床见解。
BMC Cancer. 2019 Oct 17;19(1):968. doi: 10.1186/s12885-019-6177-0.
5
Use of telomerase promoter mutations to mark specific molecular subsets with reciprocal clinical behavior in IDH mutant and IDH wild-type diffuse gliomas.在 IDH 突变型和 IDH 野生型弥漫性胶质瘤中,使用端粒酶启动子突变来标记具有相互临床行为的特定分子亚群。
J Neurosurg. 2018 Apr;128(4):1102-1114. doi: 10.3171/2016.11.JNS16973. Epub 2017 Jun 16.
6
Expression of CD70 (CD27L) Is Associated With Epithelioid and Sarcomatous Features in IDH-Wild-Type Glioblastoma.CD70(CD27L)的表达与异柠檬酸脱氢酶(IDH)野生型胶质母细胞瘤的上皮样和肉瘤样特征相关。
J Neuropathol Exp Neurol. 2017 Aug 1;76(8):697-708. doi: 10.1093/jnen/nlx051.
7
Transformation of IDH-wildtype glioblastoma to gliosarcoma with features of osteosarcoma.IDH 野生型胶质母细胞瘤向具有骨肉瘤特征的恶性纤维组织细胞瘤的转化。
Folia Neuropathol. 2024;62(1):96-101. doi: 10.5114/fn.2024.136020.
8
Genomic landscape of gliosarcoma: distinguishing features and targetable alterations.胶质肉瘤的基因组景观:鉴别特征和可靶向改变。
Sci Rep. 2021 Sep 9;11(1):18009. doi: 10.1038/s41598-021-97454-6.
9
Demographic, radiographic, molecular and clinical characteristics of primary gliosarcoma and differences to glioblastoma.原发性胶质肉瘤的人口统计学、影像学、分子及临床特征以及与胶质母细胞瘤的差异
Clin Neurol Neurosurg. 2021 Jan;200:106348. doi: 10.1016/j.clineuro.2020.106348. Epub 2020 Nov 1.
10
Isocitrate Dehydrogenase Mutations are Better Prognostic Marker than O6-methylguanine-DNA Methyltransferase Promoter Methylation in Glioblastomas - a Retrospective, Single-centre Molecular Genetics Study of Gliomas.异柠檬酸脱氢酶突变在胶质母细胞瘤中是比O6-甲基鸟嘌呤-DNA甲基转移酶启动子甲基化更好的预后标志物——一项胶质瘤的回顾性、单中心分子遗传学研究
Klin Onkol. 2017 Fall;30(5):361-371. doi: 10.14735/amko2017361.

引用本文的文献

1
A Challenging Diagnosis of Gliosarcoma: A Case Report.胶质肉瘤的疑难诊断:一例报告
Cureus. 2025 Jun 3;17(6):e85292. doi: 10.7759/cureus.85292. eCollection 2025 Jun.
2
The 2021 World Health Organization Central Nervous System Tumor Classification: The Spectrum of Diffuse Gliomas.《2021年世界卫生组织中枢神经系统肿瘤分类:弥漫性胶质瘤谱系》
Biomedicines. 2024 Jun 18;12(6):1349. doi: 10.3390/biomedicines12061349.
3
Freiburg Neuropathology Case Conference : Headache, Mental Confusion and Mild Hemiparesis in a 68-year-old Patient.
弗莱堡神经病理学病例研讨会:一名68岁患者的头痛、精神错乱和轻度偏瘫
Clin Neuroradiol. 2023 Dec;33(4):1159-1164. doi: 10.1007/s00062-023-01359-y. Epub 2023 Oct 23.
4
Gliosarcoma with direct involvement of the oculomotor nerve: Case report and literature review.直接累及动眼神经的胶质肉瘤:病例报告及文献复习
Radiol Case Rep. 2022 Feb 4;17(4):1148-1153. doi: 10.1016/j.radcr.2022.01.018. eCollection 2022 Apr.
5
Chasing a rarity: a retrospective single-center evaluation of prognostic factors in primary gliosarcoma.追求罕见:原发性胶质肉瘤预后因素的回顾性单中心评估。
Strahlenther Onkol. 2022 May;198(5):468-474. doi: 10.1007/s00066-021-01884-0. Epub 2021 Dec 22.
6
Genomic landscape of gliosarcoma: distinguishing features and targetable alterations.胶质肉瘤的基因组景观:鉴别特征和可靶向改变。
Sci Rep. 2021 Sep 9;11(1):18009. doi: 10.1038/s41598-021-97454-6.
7
Machine Learning-Based Analysis of Magnetic Resonance Radiomics for the Classification of Gliosarcoma and Glioblastoma.基于机器学习的磁共振影像组学分析用于胶质肉瘤和胶质母细胞瘤的分类
Front Oncol. 2021 Aug 20;11:699789. doi: 10.3389/fonc.2021.699789. eCollection 2021.
8
Optic pathway gliosarcoma: A very rare location for a rare disease.视神经通路胶质肉瘤:一种罕见疾病的极为罕见发病部位。
Radiol Case Rep. 2021 Apr 30;16(7):1665-1668. doi: 10.1016/j.radcr.2021.04.001. eCollection 2021 Jul.
9
Do gliosarcomas have distinct imaging features on routine MRI?胶质肉瘤在常规 MRI 上有独特的影像学特征吗?
Neuroradiol J. 2021 Oct;34(5):501-508. doi: 10.1177/19714009211012345. Epub 2021 Apr 30.
10
IDH1-mutant primary intraventricular gliosarcoma: Case report and systematic review of a rare location and molecular profile.异柠檬酸脱氢酶1(IDH1)突变型原发性脑室内胶质肉瘤:罕见部位及分子特征的病例报告与系统综述
Surg Neurol Int. 2020 Nov 6;11:372. doi: 10.25259/SNI_586_2020. eCollection 2020.