• 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

胶质肌肉瘤。一例起源于恶性神经胶质瘤的横纹肌肉瘤病例报告。

Gliomyosarcoma. Report of a case of rhabdomyosarcoma arising in a malignant glioma.

作者信息

Barnard R O, Bradford R, Scott T, Thomas D G

出版信息

Acta Neuropathol. 1986;69(1-2):23-7. doi: 10.1007/BF00687034.

DOI:10.1007/BF00687034
PMID:3962596
Abstract

The development of sarcoma within a glioblastoma is a well recognised complication: in the majority of cases it is a fibro-sarcoma originating in the tissues of the proliferating hyperplastic blood vessels. In the case described here the tumour is a rhabdomyosarcoma, apparently derived from abnormal prolific vascular mesenchyme. Only one comparable example has been recorded previously.

摘要

胶质母细胞瘤内发生肉瘤是一种公认的并发症

在大多数情况下,它是起源于增生性血管组织的纤维肉瘤。在此描述的病例中,肿瘤是横纹肌肉瘤,显然源自异常增生的血管间充质。此前仅记录过一个类似病例。

相似文献

1
Gliomyosarcoma. Report of a case of rhabdomyosarcoma arising in a malignant glioma.胶质肌肉瘤。一例起源于恶性神经胶质瘤的横纹肌肉瘤病例报告。
Acta Neuropathol. 1986;69(1-2):23-7. doi: 10.1007/BF00687034.
2
Gliomyosarcoma of the cerebrum. Report of a unique case.大脑胶质肌肉瘤。1例罕见病例报告。
Am J Clin Pathol. 1969 Dec;52(6):741-4. doi: 10.1093/ajcp/52.6.741.
3
Subependymoma with rhabdomyosarcomatous differentiation: report of a case and literature review.具有横纹肌肉瘤分化的室管膜下瘤:一例报告及文献复习
Neurosurgery. 1991 May;28(5):761-8.
4
Gliomyosarcoma: an immunohistochemical analysis.平滑肌肉瘤:免疫组织化学分析
J Neurol Neurosurg Psychiatry. 1992 Aug;55(8):728-30. doi: 10.1136/jnnp.55.8.728.
5
Mixed glioma and rhabdomyosarcoma in brain of a wild deer.一只野生鹿脑内的混合性胶质瘤和横纹肌肉瘤
Vet Pathol. 1977 Nov;14(6):643-7. doi: 10.1177/030098587701400610.
6
[On the problem of malignant gliomas of the brain. I].
Arch Geschwulstforsch. 1967;29(4):331-54.
7
[The question of medullomyoblastoma].[髓母细胞瘤的问题]
Zentralbl Allg Pathol. 1989;135(5):445-55.
8
Rhabdomyosarcoma of the brain.脑横纹肌肉瘤
J Neurosurg. 1975 Aug;43(2):215-21. doi: 10.3171/jns.1975.43.2.0215.
9
Reactive glioma in intracranial sarcoma: a form of mixed sarcoma and glioma ("sarcoglioma"): report of eight cases.颅内肉瘤中的反应性胶质瘤:一种混合性肉瘤和胶质瘤(“肉瘤样胶质瘤”)形式:8例报告
Cancer. 1979 Jan;43(1):246-57. doi: 10.1002/1097-0142(197901)43:1<246::aid-cncr2820430136>3.0.co;2-j.
10
Medulloblastoma with striated muscle fibers. Case report.伴有横纹肌纤维的髓母细胞瘤。病例报告。
J Neurosurg. 1973 May;38(5):642-6. doi: 10.3171/jns.1973.38.5.0642.

引用本文的文献

1
Clinical Characteristics of Gliosarcoma and Outcomes From Standardized Treatment Relative to Conventional Glioblastoma.胶质肉瘤的临床特征及相对于传统胶质母细胞瘤的标准化治疗结果
Front Oncol. 2019 Dec 17;9:1425. doi: 10.3389/fonc.2019.01425. eCollection 2019.
2
Brachium Pontis Gliosarcoma With Well-Differentiated Cartilaginous Tissue: A Case Report.伴有高分化软骨组织的脑桥臂胶质肉瘤:一例报告
Medicine (Baltimore). 2015 Oct;94(42):e1735. doi: 10.1097/MD.0000000000001735.
3
Primary and secondary gliosarcomas: clinical, molecular and survival characteristics.

本文引用的文献

1
Malignant peripheral nerve sheath tumors with divergent differentiation.伴有异向分化的恶性外周神经鞘瘤
Cancer. 1984 Sep 15;54(6):1049-57. doi: 10.1002/1097-0142(19840915)54:6<1049::aid-cncr2820540620>3.0.co;2-1.
2
The role of astrocytes in the formation of cartilage in gliomas. An immunohistochemical study of four cases.星形胶质细胞在胶质瘤软骨形成中的作用。4例免疫组织化学研究。
Am J Pathol. 1984 Dec;117(3):471-83.
3
Cerebral medulloepithelioma with bone, cartilage, and striated muscle. Light microscopic and immunohistochemical study.
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.
4
Malignant pediatric gliosarcoma defies general survival data.小儿恶性胶质肉瘤不符合一般的生存数据。
Case Rep Med. 2014;2014:175679. doi: 10.1155/2014/175679. Epub 2014 Dec 17.
5
Gliosarcoma: A rare primary CNS tumor. Presentation of two cases.胶质肉瘤:一种罕见的原发性中枢神经系统肿瘤。两例病例报告。
Rep Pract Oncol Radiother. 2010 Jul 7;15(4):98-102. doi: 10.1016/j.rpor.2010.05.003. eCollection 2010.
6
Neoplastic cells are a rare component in human glioblastoma microvasculature.肿瘤细胞是人类胶质母细胞瘤微血管系统中的一种罕见成分。
Oncotarget. 2012 Jan;3(1):98-106. doi: 10.18632/oncotarget.427.
7
Gliosarcoma with bone infiltration and extracranial growth: case report and review of literature.骨浸润和颅外生长的胶质肉瘤:病例报告及文献复习。
J Neurooncol. 2011 Jul;103(3):765-70. doi: 10.1007/s11060-010-0437-9. Epub 2010 Oct 19.
8
Epithelial and pseudoepithelial differentiation in glioblastoma and gliosarcoma: a comparative morphologic and molecular genetic study.胶质母细胞瘤和胶质肉瘤中的上皮及假上皮分化:一项比较形态学和分子遗传学研究
Cancer. 2008 Nov 15;113(10):2779-89. doi: 10.1002/cncr.23899.
9
Gliosarcoma with multiple extracranial metastases: case report and review of the literature.伴有多发颅外转移的胶质肉瘤:病例报告及文献综述
J Neurooncol. 2007 May;83(1):39-46. doi: 10.1007/s11060-006-9295-x. Epub 2006 Dec 14.
10
Astroblastoma in childhood: pathological and clinical analysis.儿童成星形细胞瘤:病理与临床分析
Childs Nerv Syst. 2005 Mar;21(3):211-20. doi: 10.1007/s00381-004-1055-7. Epub 2005 Jan 15.
J Neuropathol Exp Neurol. 1983 May;42(3):256-67. doi: 10.1097/00005072-198305000-00004.
4
Primary intracerebral tumor with mixed chondrosarcoma and glioblastoma--gliosarcoma or sarcoglioma?
J Neuropathol Exp Neurol. 1980 May;39(3):329-35. doi: 10.1097/00005072-198005000-00007.
5
Medullomyoblastoma. A histologic, immunohistochemical, and ultrastructural study.
Cancer. 1984 Jul 15;54(2):323-32. doi: 10.1002/1097-0142(19840715)54:2<323::aid-cncr2820540225>3.0.co;2-5.
6
Gliomyosarcoma of the cerebrum. Report of a unique case.大脑胶质肌肉瘤。1例罕见病例报告。
Am J Clin Pathol. 1969 Dec;52(6):741-4. doi: 10.1093/ajcp/52.6.741.
7
Primary rhabdomyosarcoma of the central nervous system: case report.中枢神经系统原发性横纹肌肉瘤:病例报告
Neurosurgery. 1985 Jul;17(1):101-4. doi: 10.1227/00006123-198507000-00019.
8
Cerebral mixed tumour: osteo-condrosarcoma--glioblastoma multiforme.脑混合性肿瘤:骨软骨肉瘤——多形性胶质母细胞瘤。
Acta Neurochir (Wien). 1979;50(3-4):335-41. doi: 10.1007/BF01808532.