• 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

鼻腔血管外皮瘤样肿瘤。23例临床病理研究

Hemangiopericytoma-like intranasal tumors. A clinicopathologic study of 23 cases.

作者信息

Compagno J, Hyams V J

出版信息

Am J Clin Pathol. 1976 Oct;66(4):672-83. doi: 10.1093/ajcp/66.4.672.

DOI:10.1093/ajcp/66.4.672
PMID:970369
Abstract

The clinical, microscopic, and gross pathologic features of 23 cases of intranasal hemangiopericytoma-like tumors are reviewed and studied. When in the nasal cavity, these lesions often originated in a paranasal sinus and extended into the nasal cavity secondarily. They occurred most commonly in adults in the sixth and seventh decades of life; there was no significant sex predilection. Twenty-two of the 23 patients were Caucasian. These patients most commonly had symptoms of nasal obstruction and epistaxis. Clinically the lesions were generally thought to represent allergic polyps. Although appearing microscopically as non-differentiated spindle-cell neoplasms, these lesions showed little nuclear or cytoplasmic pleomorphism, minimal mitotic activity, and no necrosis or hemorrhage or other evidence of anaplasia found in malignant tumors. Follow-up data showed no evidence to suggest a malignant or biologically unpredictable lesion. Nineteen of 22 cases followed showed no recurrence regardless of the treatment; those that recurred did so locally. No metastasis or other form of aggressive behavior attributed to hemangiopericytomas in other anatomic locations was seen in this series. Another case, diagnosed as a malignant hemangiopericytoma of the nasal cavity, showed dissimilar and anaplastic histologic features. This case metastasized and is discussed, though not included in this study.

摘要

对23例鼻腔血管外皮细胞瘤样肿瘤的临床、显微镜下及大体病理特征进行了回顾和研究。当位于鼻腔时,这些病变常起源于鼻窦,继而延伸至鼻腔。它们最常见于60和70岁的成年人;无明显性别倾向。23例患者中有22例为白种人。这些患者最常见的症状是鼻塞和鼻出血。临床上这些病变通常被认为是过敏性息肉。尽管在显微镜下表现为未分化的梭形细胞肿瘤,但这些病变几乎没有核或胞质多形性,有丝分裂活动极少,且未发现恶性肿瘤中出现的坏死、出血或其他间变证据。随访数据显示,没有证据表明这些病变具有恶性或生物学上不可预测性。22例接受随访的病例中,19例无论接受何种治疗均未复发;复发的病例均为局部复发。本系列中未观察到其他解剖部位血管外皮细胞瘤所具有的转移或其他侵袭性行为。另一例被诊断为鼻腔恶性血管外皮细胞瘤的病例,表现出不同的间变组织学特征。该病例发生了转移并进行了讨论,但未纳入本研究。

相似文献

1
Hemangiopericytoma-like intranasal tumors. A clinicopathologic study of 23 cases.鼻腔血管外皮瘤样肿瘤。23例临床病理研究
Am J Clin Pathol. 1976 Oct;66(4):672-83. doi: 10.1093/ajcp/66.4.672.
2
Hemangiopericytoma-like tumors of the nasal cavity: a comparison with hemangiopericytoma of soft tissues.鼻腔血管外皮细胞瘤样肿瘤:与软组织血管外皮细胞瘤的比较
Laryngoscope. 1978 Mar;88(3):460-9. doi: 10.1288/00005537-197803000-00010.
3
[Clinical analysis of sinonasal hemangiopericytoma].[鼻窦血管外皮细胞瘤的临床分析]
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2014 Jun;49(6):452-6.
4
[2 cases of hemangiopericytoma of the maxilla and nose].上颌骨及鼻血管外皮细胞瘤2例
Otolaryngol Pol. 1982;36(5-6):365-71.
5
Sinonasal hemangiopericytoma. A reassessment with electron microscopy, immunohistochemistry, and long-term follow-up.
Am J Surg Pathol. 1990 Sep;14(9):856-66.
6
[Hemangiopericytoma in nasal cavity: a case report].[鼻腔血管外皮细胞瘤:一例报告]
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2015 May;29(9):853-4.
7
Sinonasal-type hemangiopericytoma: a clinicopathologic and immunophenotypic analysis of 104 cases showing perivascular myoid differentiation.鼻窦型血管外皮细胞瘤:104例显示血管周肌样分化的临床病理及免疫表型分析
Am J Surg Pathol. 2003 Jun;27(6):737-49. doi: 10.1097/00000478-200306000-00004.
8
Sino-nasal hemangiopericytoma--a rare tumor.鼻窦血管外皮细胞瘤——一种罕见肿瘤。
Med J Malaysia. 2005 Oct;60(4):485-8.
9
[Sinonasal hemangiopericytoma].
HNO. 2004 Dec;52(12):1091-6. doi: 10.1007/s00106-003-1030-8.
10
Nasal haemangiopericytoma.鼻腔血管外皮细胞瘤
J Laryngol Otol. 1991 Jul;105(7):593-5. doi: 10.1017/s0022215100116718.

引用本文的文献

1
A Hemangiopericytoma in the External Auditory Canal: A Rare Clinical Presentation and Management.外耳道血管外皮细胞瘤:一种罕见的临床表现及处理
Cureus. 2024 Sep 4;16(9):e68676. doi: 10.7759/cureus.68676. eCollection 2024 Sep.
2
Breaking New Ground: Unraveling Sinonasal Hemangiopericytoma Through a Rare Case Series on Endoscopic Excision and Postoperative Monitoring.开辟新天地:通过一组罕见的内镜切除及术后监测病例系列解析鼻窦血管外皮细胞瘤
Indian J Otolaryngol Head Neck Surg. 2024 Aug;76(4):3369-3373. doi: 10.1007/s12070-024-04692-x. Epub 2024 Apr 29.
3
Glomangiopericytoma with mutation.
伴 突变的血管外皮细胞瘤。
BMJ Case Rep. 2023 Sep 18;16(9):e256787. doi: 10.1136/bcr-2023-256787.
4
Clinical and histopathological findings of a rare sinonasal glomangiopericytoma.一例罕见鼻窦血管外皮细胞瘤的临床及组织病理学表现
Autops Case Rep. 2023 Apr 10;13:e2023424. doi: 10.4322/acr.2023.424. eCollection 2023.
5
Endoscopic Excision of Sino Nasal Hemangiopericytoma.鼻腔鼻窦血管外皮细胞瘤的内镜下切除
Indian J Otolaryngol Head Neck Surg. 2022 Oct;74(Suppl 2):1274-1280. doi: 10.1007/s12070-021-02387-1. Epub 2021 Jan 26.
6
CT and MRI Findings of Glomangiopericytoma in the Head and Neck: Case Series Study and Systematic Review.头颈部血管外皮细胞瘤的 CT 和 MRI 表现:病例系列研究和系统评价。
AJNR Am J Neuroradiol. 2020 Jan;41(1):155-159. doi: 10.3174/ajnr.A6336. Epub 2019 Dec 5.
7
β-catenin (CTNNB1) mutation and LEF1 expression in sinonasal glomangiopericytoma (sinonasal-type hemangiopericytoma).β-连环蛋白(CTNNB1)突变和 LEF1 表达在鼻腔鼻窦血管外皮细胞瘤(鼻腔鼻窦型血管外皮细胞瘤)中。
Virchows Arch. 2018 Aug;473(2):235-239. doi: 10.1007/s00428-018-2370-9. Epub 2018 May 7.
8
Glomangiopericytoma of the Spinal Cord.脊髓血管外皮细胞瘤
Korean J Spine. 2017 Dec;14(4):166-169. doi: 10.14245/kjs.2017.14.4.166. Epub 2017 Dec 31.
9
Update on Select Benign Mesenchymal and Meningothelial Sinonasal Tract Lesions.鼻腔鼻窦良性间叶组织及脑膜上皮性病变的最新进展
Head Neck Pathol. 2016 Mar;10(1):95-108. doi: 10.1007/s12105-016-0697-6. Epub 2016 Feb 1.
10
Nuclear expression and gain-of-function β-catenin mutation in glomangiopericytoma (sinonasal-type hemangiopericytoma): insight into pathogenesis and a diagnostic marker.肾小球血管外皮细胞瘤(鼻窦型血管外皮细胞瘤)中的核表达及功能获得性β-连环蛋白突变:对发病机制的见解及一种诊断标志物
Mod Pathol. 2015 May;28(5):715-20. doi: 10.1038/modpathol.2014.161. Epub 2014 Nov 28.