• 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

幕上皮样囊肿。5例病例的表现与处理

Supratentorial dermoid cysts. Presentation and management of five cases.

作者信息

Bucciero A, Del Basso De Caro M L, Carraturo S, Vizioli L, Cerillo A, Tedeschi G

机构信息

Chair of Neurosurgery, 2nd School of Medicine, University of Naples, Italy.

出版信息

J Neurosurg Sci. 1995 Mar;39(1):7-11.

PMID:8568557
Abstract

Five patients with supratentorial dermoid cysts who were surgically treated are presented. There were three males and two females, between the ages of 17 and 35 years (mean 26.6 years). The tumor location was frontobasal and/or temporobasal. The duration of illness before the diagnosis ranged from 1 to 14 months (mean 7.4 months). Clinical presentation included seizures, intracranial hypertension syndrome, aseptic meningitis, homonimous lateral hemianopsia, and memory defect. Preoperatively, all patients were investigated by computerized tomography (CT); in two cases, magnetic resonance (MR) imaging was also obtained. Tumor removal was performed by microsurgical procedures; it was total in 3 cases and subtotal in the remaining 2 cases. Histologically, all of the tumors exhibited the typical dermoid cyst pattern. There were no operative deaths. Two patients experienced postoperative language dysfunction and/or hemiparesis. No patient developed clinicoradiological evidence of tumor recurrence at 1 to 10 years (mean 5 years) following surgery. These results are discussed in light of the data previously reported by the literature.

摘要

本文报告了5例接受手术治疗的幕上皮样囊肿患者。其中男性3例,女性2例,年龄在17至35岁之间(平均26.6岁)。肿瘤位于额底部和/或颞底部。诊断前的病程为1至14个月(平均7.4个月)。临床表现包括癫痫发作、颅内高压综合征、无菌性脑膜炎、同向性偏盲和记忆缺陷。术前,所有患者均接受了计算机断层扫描(CT)检查;2例还进行了磁共振(MR)成像检查。肿瘤切除采用显微外科手术;3例全切,其余2例次全切。组织学上,所有肿瘤均表现为典型的皮样囊肿模式。无手术死亡病例。2例患者术后出现语言功能障碍和/或偏瘫。术后1至10年(平均5年),无患者出现肿瘤复发的临床和影像学证据。结合文献先前报道的数据对这些结果进行了讨论。

相似文献

1
Supratentorial dermoid cysts. Presentation and management of five cases.幕上皮样囊肿。5例病例的表现与处理
J Neurosurg Sci. 1995 Mar;39(1):7-11.
2
[Intracranial epidermoid and dermoid cysts].[颅内表皮样囊肿和皮样囊肿]
Rev Neurol. 1998 Nov;27(159):777-82.
3
Rare Case of Giant Supratentorial Dermoid Cyst.罕见的巨大幕上皮样囊肿病例。
World Neurosurg. 2020 Mar;135:72-75. doi: 10.1016/j.wneu.2019.12.007. Epub 2019 Dec 9.
4
Supratentorial dermoid cysts.
J Neurosurg. 1991 Aug;75(2):262-6. doi: 10.3171/jns.1991.75.2.0262.
5
Intracranial dermoid cysts: variations of radiological and clinical features.颅内皮样囊肿:放射学和临床特征的变异
Acta Neurochir (Wien). 2008 Dec;150(12):1227-34; discussion 1234. doi: 10.1007/s00701-008-0152-x. Epub 2008 Nov 20.
6
Temporal dermoid cyst with a partial dermal sinus tract.伴有部分皮样窦道的颞部皮样囊肿。
Can J Neurol Sci. 1999 Nov;26(4):321-4. doi: 10.1017/s0317167100000470.
7
Microneurosurgical treatment of intracranial dermoid and epidermoid tumors.颅内皮样囊肿和表皮样囊肿的显微神经外科治疗。
Neurosurgery. 1989 Apr;24(4):561-7. doi: 10.1227/00006123-198904000-00012.
8
Intracranial midline dermoid and epidermoid cysts in children.儿童颅内中线皮样囊肿和表皮样囊肿
J Neurosurg. 2004 May;100(5 Suppl Pediatrics):473-80. doi: 10.3171/ped.2004.100.5.0473.
9
[Subarachnoid rupture of supratentorial dermoid cyst: CT and MRI aspects].[幕上皮样囊肿的蛛网膜下腔破裂:CT与MRI表现]
J Radiol. 1996 Dec;77(12):1237-9.
10
Ruptured intracranial dermoid cysts: clinical, radiographic, and surgical features.破裂的颅内皮样囊肿:临床、影像学及手术特征
Neurosurgery. 2008 Feb;62(2):377-84; discussion 384. doi: 10.1227/01.neu.0000316004.88517.29.

引用本文的文献

1
Postoperative Symptomatic Cerebral Vasospasm: Requiring Attention Following an Uneventful Resection of an Epidermoid Cyst - A Case Report and Literature Review.术后症状性脑血管痉挛:表皮样囊肿顺利切除后需引起关注——病例报告及文献综述
NMC Case Rep J. 2024 Jul 27;11:195-200. doi: 10.2176/jns-nmc.2023-0259. eCollection 2024.