• 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

中枢神经细胞瘤的鉴别诊断:两例报告。

Differential Diagnosis of Central Neurocytoma: Two Cases.

机构信息

Department of Neurosurgery, Kantonsspital St. Gallen, St. Gallen, Switzerland.

Institute of Pathology, Kantonsspital St. Gallen, St. Gallen, Switzerland.

出版信息

J Neurol Surg A Cent Eur Neurosurg. 2021 Nov;82(6):599-603. doi: 10.1055/s-0040-1718693. Epub 2020 Dec 22.

DOI:10.1055/s-0040-1718693
PMID:33352608
Abstract

Central neurocytoma are rare primary brain tumors of the young and middle-aged adult, typically located in the lateral ventricles. Diagnosis has historically been difficult due to histomorphologic similarities to oligodendroglioma and ependymal tumors and remains a challenge even today. We present two cases of intraventricular central neurocytoma in which careful consideration of the clinical and radiological findings led to reevaluation of the preliminary histological interpretation, highlighting the importance of a meticulous differential diagnosis.

摘要

中枢神经细胞瘤是一种罕见的青年和中年人群原发性脑肿瘤,通常位于侧脑室。由于其组织形态学与少突胶质细胞瘤和室管膜肿瘤相似,历史上诊断较为困难,即使在今天,这仍然是一个挑战。我们报告了两例脑室中央神经细胞瘤,仔细考虑了临床和影像学发现,导致对初步组织学解释的重新评估,突出了细致鉴别诊断的重要性。

相似文献

1
Differential Diagnosis of Central Neurocytoma: Two Cases.中枢神经细胞瘤的鉴别诊断:两例报告。
J Neurol Surg A Cent Eur Neurosurg. 2021 Nov;82(6):599-603. doi: 10.1055/s-0040-1718693. Epub 2020 Dec 22.
2
Intraoperative imprint cytology of central neurocytoma: The great oligodendroglioma mimicker.中枢神经细胞瘤的术中印片细胞学检查:酷似少突胶质细胞瘤的疾病。
Diagn Cytopathol. 2010 Mar;38(3):202-7. doi: 10.1002/dc.21179.
3
[Central neurocytoma: case report].[中枢神经细胞瘤:病例报告]
J Radiol. 2003 Jul-Aug;84(7-8 Pt 1):855-6.
4
Extraventricular neurocytoma in a child: case report and review of the literature.儿童脑室外神经细胞瘤:病例报告及文献复习
J Child Neurol. 2009 Apr;24(4):491-4. doi: 10.1177/0883073808324534.
5
Central neurocytoma: clinico-pathological study of 5 cases and review of the literature.中枢神经细胞瘤:5例临床病理研究及文献复习
Clin Neurol Neurosurg. 1995 Aug;97(3):219-28. doi: 10.1016/0303-8467(95)00031-e.
6
Extraventricular neurocytoma in a child mimicking oligodendroglioma: a diagnostic pitfall.儿童室管膜外神经细胞瘤酷似少突胶质细胞瘤:一个诊断陷阱。
Pathologica. 2009 Apr;101(2):105-7.
7
Central Neurocytoma: Rare Presentation in Fourth Ventricle and Review of Literature.中枢神经细胞瘤:第四脑室的罕见表现及文献综述
World Neurosurg. 2019 Mar;123:357-361. doi: 10.1016/j.wneu.2018.12.021. Epub 2018 Dec 19.
8
Extraventricular neurocytoma: morphological and immunohistochemical considerations on differential diagnosis.脑室外神经细胞瘤:鉴别诊断的形态学及免疫组化考量
Pathol Res Pract. 2002;198(9):627-33; discussion 635-8. doi: 10.1078/0344-0338-00312.
9
Cytologic diagnosis of central neurocytoma in intraoperative squash preparations: a report of 2 cases.术中压片标本中枢神经细胞瘤的细胞学诊断:2例报告
Acta Cytol. 2010 Mar-Apr;54(2):209-13. doi: 10.1159/000325012.
10
Transcortical Approach to Deep-Seated Intraventricular and Intra-axial Tumors Using a Tubular Retractor System: A Technical Note and Review of the Literature.经皮质入路应用管状牵开器系统切除脑室内深部和脑内肿瘤:技术要点及文献复习
J Neurol Surg A Cent Eur Neurosurg. 2021 May;82(3):270-277. doi: 10.1055/s-0040-1719025. Epub 2020 Dec 15.

引用本文的文献

1
Rare Neuronal, Glial and Glioneuronal Tumours in Adults.成人罕见的神经元、神经胶质和神经胶质神经元肿瘤。
Cancers (Basel). 2023 Feb 9;15(4):1120. doi: 10.3390/cancers15041120.
2
Clinical prognostic factors for central neurocytoma and subgroup analysis of different treatment measures: A SEER database-based retrospective analysis from 2003 to 2019.中枢神经细胞瘤的临床预后因素及不同治疗措施的亚组分析:基于2003年至2019年监测、流行病学和最终结果(SEER)数据库的回顾性分析
Front Oncol. 2023 Jan 6;12:1014506. doi: 10.3389/fonc.2022.1014506. eCollection 2022.
3
A rare presentation of primary lateral ventricle H3 K27-altered diffuse midline glioma in a 14-year-old girl: a case description.
一名14岁女孩原发性侧脑室H3 K27改变的弥漫性中线胶质瘤的罕见表现:病例描述
Quant Imaging Med Surg. 2022 Nov;12(11):5288-5295. doi: 10.21037/qims-22-339.