• 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

[外周神经外间充质瘤(神经外间充质瘤):一种由神经嵴成分构成的恶性肿瘤]

[Peripheral nerve ectomesenchymoma (neuroectomesenchymoma): a malignant tumor made up of neural crest elements].

作者信息

Galil-Ogly G A, Poroshin K K, Krylov L M

出版信息

Arkh Patol. 1981;43(10):33-40.

PMID:7316824
Abstract

Characteristics of a little-studied tumor of soft tissues are described on the basis of the author's own material (4 observations) and data from the literature. The matter at issue is a benign or malignant schwannoma (less frequently, ganglioneuroblastoma) in which there are areas of rhabdomyosarcoma and sometimes tumor elements of mesenchymal origin (angio- lipo-, or osteogenic sarcoma). As a rule, this tumor is located along the peripheral nerve or arises in one of the nodes in Recklinghausen's disease and has a trend to hematogenic metastasising. It is suggested that the source of growth of neoplasias of this kind are the cells of "neural crest" migrating in the process of embryogenesis. These cells are responsible for the formation of lemmocytes, ganglial elements and melanocytes, as well as ectomesenchyma from which, in its turn, a part of cross-striated musculature is formed. Therefore, the tumors described in the paper should be designated as "neuroectomesenchymoma" (according to some authors, ectomesenchymoma).

摘要

基于作者自己的资料(4例观察)以及文献数据,描述了一种研究较少的软组织肿瘤的特征。讨论的问题是一种良性或恶性神经鞘瘤(较少见的是神经节神经母细胞瘤),其中存在横纹肌肉瘤区域,有时还有间充质起源的肿瘤成分(血管脂肪肉瘤或骨肉瘤)。通常,这种肿瘤沿周围神经分布或发生于冯雷克林霍增氏病的一个结节中,并有血行转移倾向。提示这类肿瘤的生长来源是胚胎发育过程中迁移的“神经嵴”细胞。这些细胞负责形成雪旺细胞、神经节成分和黑素细胞,以及外间充质,进而由外间充质形成部分横纹肌组织。因此,本文所述肿瘤应命名为“神经外间充质瘤”(根据一些作者的说法,外间充质瘤)。

相似文献

1
[Peripheral nerve ectomesenchymoma (neuroectomesenchymoma): a malignant tumor made up of neural crest elements].[外周神经外间充质瘤(神经外间充质瘤):一种由神经嵴成分构成的恶性肿瘤]
Arkh Patol. 1981;43(10):33-40.
2
Malignant mesenchymoma of ulnar nerve: combined sarcoma of nerve sheath and rhabdomyosarcoma.尺神经恶性间叶瘤:神经鞘肉瘤与横纹肌肉瘤的联合肉瘤
J Neurol Neurosurg Psychiatry. 1979 Jun;42(6):524-8. doi: 10.1136/jnnp.42.6.524.
3
Molecular array analyses of 51 pediatric tumors shows overlap between malignant intracranial ectomesenchymoma and MPNST but not medulloblastoma or atypical teratoid rhabdoid tumor.对51例儿科肿瘤进行的分子阵列分析显示,恶性颅内外胚层间叶瘤与恶性周围神经鞘膜瘤之间存在重叠,但与髓母细胞瘤或非典型畸胎样横纹肌样瘤不存在重叠。
Acta Neuropathol. 2007 Jun;113(6):695-703. doi: 10.1007/s00401-007-0210-0. Epub 2007 Mar 13.
4
Actin expression in neural crest cell-derived tumors including schwannomas, malignant peripheral nerve sheath tumors, neurofibromas and melanocytic tumors.肌动蛋白在神经嵴细胞衍生肿瘤中的表达,包括神经鞘瘤、恶性外周神经鞘膜瘤、神经纤维瘤和黑素细胞肿瘤。
Pathol Int. 2009 Feb;59(2):86-90. doi: 10.1111/j.1440-1827.2008.02333.x.
5
Primary malignant ectomesenchymoma of the orbit.眼眶原发性恶性外间充质瘤。
Gen Diagn Pathol. 1997 Feb;142(3-4):221-5.
6
Ectomesenchymoma. A malignant tumor of migratory neural crest (ectomesenchyme) remnants showing ganglionic, schwannian, melanocytic and rhabdomyoblastic differentiation.外胚间叶瘤。一种起源于迁移性神经嵴(外胚间叶组织)残余物的恶性肿瘤,表现为神经节、施万细胞、黑素细胞和成横纹肌细胞分化。
Cancer. 1977 Jun;39(6):2486-96. doi: 10.1002/1097-0142(197706)39:6<2486::aid-cncr2820390627>3.0.co;2-e.
7
[Apropos of a case of malignant schwannoma with rhabdomyoblastic components. Malignant Triton tumor].
Arch Anat Cytol Pathol. 1988;36(4):175-7.
8
[Pelvic malignant ectomesenchymoma: a case report].[盆腔恶性外间叶瘤:一例报告]
Ann Pathol. 2001 Aug;21(4):344-7.
9
Malignant peripheral nerve sheath tumor of the breast: case report.乳腺恶性外周神经鞘膜瘤:病例报告
World J Surg Oncol. 2007 Dec 21;5:142. doi: 10.1186/1477-7819-5-142.
10
Ectomesenchymoma with embryonal rhabdomyosarcoma and ganglioneuroma, arising in association with benign triton tumor of the tongue.伴有胚胎性横纹肌肉瘤和神经节神经瘤的外间充质瘤,与舌部良性蝾螈瘤相关联发生。
Pediatr Dev Pathol. 2014 May-Jun;17(3):226-30. doi: 10.2350/14-01-1433-CR.1. Epub 2014 Mar 20.