• 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

Spontaneous regression of a congenital high-grade glioma-a case report.

作者信息

Riedmeier Maria, Stock Annika, Krauß Jürgen, Sahm Felix, Jones David T W, Sturm Dominik, Kramm Christof M, Eyrich Matthias, Härtel Christoph, Schlegel Simon, Schlegel Paul Gerhardt, Monoranu Camelia-Maria, Wiegering Verena

机构信息

Department of Pediatric Hematology, Oncology and Stem Cell Transplantation, University Children's Hospital, University of Würzburg, Würzburg, Germany.

Department of Neuroradiology, University Hospital, University of Würzburg, Würzburg, Germany.

出版信息

Neurooncol Adv. 2021 Aug 25;3(1):vdab120. doi: 10.1093/noajnl/vdab120. eCollection 2021 Jan-Dec.

DOI:10.1093/noajnl/vdab120
PMID:34704035
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8541705/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f1/8541705/64229dc03758/vdab120f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f1/8541705/0acb291c3503/vdab120f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f1/8541705/e987d29e7da7/vdab120f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f1/8541705/64229dc03758/vdab120f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f1/8541705/0acb291c3503/vdab120f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f1/8541705/e987d29e7da7/vdab120f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f1/8541705/64229dc03758/vdab120f0003.jpg

相似文献

1
Spontaneous regression of a congenital high-grade glioma-a case report.先天性高级别胶质瘤的自发消退——病例报告
Neurooncol Adv. 2021 Aug 25;3(1):vdab120. doi: 10.1093/noajnl/vdab120. eCollection 2021 Jan-Dec.
2
Spontaneous complete regression of a brain stem glioma pathologically diagnosed as a high-grade glioma.一例经病理诊断为高级别胶质瘤的脑干胶质瘤自发完全消退。
Childs Nerv Syst. 2017 Dec;33(12):2177-2180. doi: 10.1007/s00381-017-3570-3. Epub 2017 Aug 14.
3
A Case of Congenital Malignant Spinal Cord Glioma as a Cause of Congenital Ascites in a Neonate.一例先天性恶性脊髓胶质瘤导致新生儿先天性腹水的病例。
Case Rep Pediatr. 2016;2016:5208753. doi: 10.1155/2016/5208753. Epub 2016 Aug 14.
4
Progression of Low-Grade Glioma During Pregnancy With Subsequent Regression Postpartum Without Treatment-A Case Report.妊娠期低级别胶质瘤进展，产后未经治疗自行消退——1 例报告
Neurosurgery. 2019 Jun 1;84(6):E430-E436. doi: 10.1093/neuros/nyy191.
5
Resolving mystery behind autonomous retrogression of low-grade gliomas: A systematic review.
J Pak Med Assoc. 2020 Dec;70(12(B)):2441-2448. doi: 10.47391/JPMA.581.
6
Occurrence of high-grade glioma in Noonan syndrome: Report of two cases.Noonan 综合征中高级别胶质瘤的发生：两例报告。
Pediatr Blood Cancer. 2019 May;66(5):e27625. doi: 10.1002/pbc.27625. Epub 2019 Jan 28.
7
Antigenic expression and spontaneous immune responses support the use of a selected peptide set from the IMA950 glioblastoma vaccine for immunotherapy of grade II and III glioma.抗原表达和自发免疫反应支持使用从IMA950胶质母细胞瘤疫苗中挑选的一组肽用于II级和III级胶质瘤的免疫治疗。
Oncoimmunology. 2017 Nov 7;7(2):e1391972. doi: 10.1080/2162402X.2017.1391972. eCollection 2018.
8
Regression of Recurrent High-Grade Glioma with Temozolomide, Dexamethasone, and Levetiracetam: Case Report and Review of the Literature.替莫唑胺、地塞米松和左乙拉西坦治疗复发性高级别胶质瘤的疗效：病例报告及文献综述
World Neurosurg. 2017 Dec;108:990.e11-990.e16. doi: 10.1016/j.wneu.2017.08.136. Epub 2017 Sep 1.
9
Regression of Recurrent Spinal Cord High-Grade Glioma After Convection-Enhanced Delivery of Nimustine Hydrochloride: Case Reports and Literature Review.
Oper Neurosurg. 2020 Apr 1;18(4):451-459. doi: 10.1093/ons/opz172.
10
Identification and validation of an individualized prognostic signature of lower-grade glioma based on nine immune related long non-coding RNA.基于九个免疫相关长链非编码RNA的低级别胶质瘤个体化预后标志物的鉴定与验证
Clin Neurol Neurosurg. 2021 Feb;201:106464. doi: 10.1016/j.clineuro.2020.106464. Epub 2021 Jan 5.

引用本文的文献

1
Rare Oncogenic Fusions in Pediatric Central Nervous System Tumors: A Case Series and Literature Review.儿童中枢神经系统肿瘤中的罕见致癌融合：病例系列及文献综述
Cancers (Basel). 2024 Sep 30;16(19):3344. doi: 10.3390/cancers16193344.
2
Clinical, pathologic, and genomic characteristics of two pediatric glioneuronal tumors with a CLIP2::MET fusion.具有 CLIP2::MET 融合的两例儿科胶质神经元肿瘤的临床、病理和基因组特征。
Acta Neuropathol Commun. 2024 Apr 22;12(1):63. doi: 10.1186/s40478-024-01776-1.

本文引用的文献

1
A glioneuronal tumor with fusion.一种伴有融合的神经胶质神经元肿瘤。
NPJ Genom Med. 2020 Jun 3;5:24. doi: 10.1038/s41525-020-0131-6. eCollection 2020.
2
Infant High-Grade Gliomas Comprise Multiple Subgroups Characterized by Novel Targetable Gene Fusions and Favorable Outcomes.婴儿高级别神经胶质瘤包含多个亚组，其特征为新型可靶向基因融合和良好的预后。
Cancer Discov. 2020 Jul;10(7):942-963. doi: 10.1158/2159-8290.CD-19-1030. Epub 2020 Apr 1.
3
Targetable molecular alterations in congenital glioblastoma.先天性神经胶质瘤的靶向分子改变。
J Neurooncol. 2020 Jan;146(2):247-252. doi: 10.1007/s11060-019-03377-8. Epub 2019 Dec 24.
4
Alterations in ALK/ROS1/NTRK/MET drive a group of infantile hemispheric gliomas.ALK/ROS1/NTRK/MET 改变驱动一组婴儿半球胶质瘤。
Nat Commun. 2019 Sep 25;10(1):4343. doi: 10.1038/s41467-019-12187-5.
5
Spontaneous regression of neuroblastoma.神经母细胞瘤的自发消退。
Cell Tissue Res. 2018 May;372(2):277-286. doi: 10.1007/s00441-017-2761-2. Epub 2018 Jan 5.
6
Perinatal (fetal and neonatal) astrocytoma: a review.围产期（胎儿和新生儿）星形细胞瘤：综述
Childs Nerv Syst. 2016 Nov;32(11):2085-2096. doi: 10.1007/s00381-016-3215-y. Epub 2016 Aug 27.