实用肿瘤学杂志 ›› 2013, Vol. 27 ›› Issue (5): 433-435.doi: 10.3969/j.issn.1002-3070.2013.05.012

• 个案 • 上一篇    下一篇

伸长细胞型室管膜瘤1例报告

陈立强1,胡帅2,李文忠1,陈大伟1,罗毅男1   

  1. 1.吉林大学第一医院神经外科(长春 130021)
    2.大连医科大学附属第一医院神经内科
  • 收稿日期:2013-04-09 出版日期:2013-10-28 发布日期:2013-10-15
  • 通讯作者: 罗毅男,E-mail:northcliffs@126.com
  • 作者简介:陈立强,男,(1986-),硕士研究生,从事神经系统肿瘤的临床与基础研究

A case report of tanycytic ependymoma

CHEN Liqiang1,HU Shuai2,LI Wenzhong1,CHEN Dawei1,LUO Yinan1   

  1. 1.First Hospital of Jilin University,changchun 130021,China
    2.The official First Affiliated Hospital of Dalian Medical University
  • Received:2013-04-09 Online:2013-10-28 Published:2013-10-15

摘要: 通过分析吉林大学第一医院1例确诊为伸长细胞型室管膜瘤患者的临床资料,整理近期国内外关于伸长细胞型室管膜瘤的相关文献。我们可以得出伸长细胞型室管膜瘤十分罕见,多来源于脑室壁和脊髓中央管表面室管膜瘤细胞,缺乏特征性影像学表现,以压迫而不是侵犯脑和脊髓组织为主要临床表现,室管膜瘤的治疗方案是手术中容易达到的部位全切肿瘤结合术后放疗治疗。伸长细胞型室管膜瘤手术后预后尚需进一步观察。

Abstract: To report a case of tanycytic ependymoma and to review the interrelated articles.Our Conclusion is that tanycytic ependymoma is rare.TE derives mainly from paraventricular and spinal ependymoma central tube surface cells,which is lack of characteristic imaging findings.The main clinical manifestations is to oppress but not brain and spinal cord tissue .Tanycytic Ependymoma treatment is tumorectomy ecteug combined with postoperative radiation therapy.Tanycytic ependymoma prognosis after surgery still needs further observation.

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