• 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

皮肤复合性血管内皮瘤:病例报告及已发表报告综述

Cutaneous composite hemangioendothelioma: case report and review of published reports.

作者信息

Stojsic Zorica, Brasanac Dimitrije, Stojanovic Martina, Boricic Mladen

机构信息

Dr. Dimitrije Brasanac, Institute of Pathology,, Faculty of Medicine,, University of Belgrade,, Belgrade 11000, Serbia, T: +381.11-3643410;, F: +381-11-3643346,

出版信息

Ann Saudi Med. 2014 Mar-Apr;34(2):182-8. doi: 10.5144/0256-4947.2014.182.

DOI:10.5144/0256-4947.2014.182
PMID:24894791
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6074862/
Abstract

Composite hemangioendothelioma (CHE) is a rare, locally aggressive, vascular tumor of intermediate-/ low-grade malignancy, and is characterized by varying combinations of benign, low-grade malignant, and malignant vascular components. In cutaneous localization, only 22 cases have been reported so far. A new case of CHE of the gluteal region in a 58-year-old man is described. Microscopically, vascular neoplasm, situated mainly within the deep dermis and the subcutaneous fat tissue, was composed of sinusoidal hemangioma, arteriovenous hemangioma, retiform hemangioendothelioma (RHE), and angiosarcoma. An average number of mitoses within the angiosarcomatous component was 10 per 10 high-power fields. Immunohistochemically, the tumor cells were positive for factor VIII-related antigen, CD34, and CD31 and negative for D2-40 and GLUT-1. Ki-67 labeling index was 21%, 1.2%, and 0% in the areas of angiosarcoma, RHE, and sinusoidal hemangioma, respectively. No recurrent disease was noted 3 months after the surgery. The present case displayed the following features previously undescribed in CHE: a novel component of sinusoidal hemangioma and localization at the gluteal region. We also provide review of clinical, histopathological, and immunohistochemical characteristics of cutaneous CHE from the published cases.

摘要

复合性血管内皮瘤(CHE)是一种罕见的、局部侵袭性的、中/低级别恶性的血管肿瘤,其特征是良性、低级别恶性和恶性血管成分的不同组合。在皮肤定位方面,迄今为止仅报道了22例。本文描述了一名58岁男性臀区CHE的新病例。显微镜下,血管肿瘤主要位于真皮深层和皮下脂肪组织内,由窦性血管瘤、动静脉血管瘤、网状血管内皮瘤(RHE)和血管肉瘤组成。血管肉瘤成分内每10个高倍视野的平均有丝分裂数为10个。免疫组化显示,肿瘤细胞因子VIII相关抗原、CD34和CD31呈阳性,D2-40和GLUT-1呈阴性。在血管肉瘤、RHE和窦性血管瘤区域,Ki-67标记指数分别为21%、1.2%和0%。术后3个月未发现复发病例。本病例表现出CHE以前未描述的以下特征:窦性血管瘤的新成分和臀区定位。我们还对已发表病例中皮肤CHE的临床、组织病理学和免疫组化特征进行了综述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1242/6074862/fc9a804739b0/asm-2-182f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1242/6074862/77c46a676ca2/asm-2-182f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1242/6074862/7201f8141517/asm-2-182f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1242/6074862/6106b5c8f25a/asm-2-182f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1242/6074862/6e0476b59dc6/asm-2-182f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1242/6074862/fc9a804739b0/asm-2-182f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1242/6074862/77c46a676ca2/asm-2-182f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1242/6074862/7201f8141517/asm-2-182f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1242/6074862/6106b5c8f25a/asm-2-182f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1242/6074862/6e0476b59dc6/asm-2-182f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1242/6074862/fc9a804739b0/asm-2-182f5.jpg

相似文献

1
Cutaneous composite hemangioendothelioma: case report and review of published reports.皮肤复合性血管内皮瘤:病例报告及已发表报告综述
Ann Saudi Med. 2014 Mar-Apr;34(2):182-8. doi: 10.5144/0256-4947.2014.182.
2
Composite hemangioendothelioma arising from the kidney: case report with review of the literature.起源于肾脏的复合性血管内皮瘤:病例报告并文献复习
Int J Clin Exp Pathol. 2013 Aug 15;6(9):1935-41. eCollection 2013.
3
Composite hemangioendothelioma: report of 5 cases including one with associated Maffucci syndrome.复合性血管内皮瘤:5例报告,其中1例伴有马富西综合征。
Am J Surg Pathol. 2007 Oct;31(10):1567-72. doi: 10.1097/PAS.0b013e318038f6b5.
4
Spindle cell hemangioendothelioma. A low-grade angiosarcoma resembling a cavernous hemangioma and Kaposi's sarcoma.梭形细胞血管内皮瘤。一种类似于海绵状血管瘤和卡波西肉瘤的低级别血管肉瘤。
Am J Surg Pathol. 1986 Aug;10(8):521-30.
5
Recurrent YAP1 and MAML2 Gene Rearrangements in Retiform and Composite Hemangioendothelioma.复发性 YAP1 和 MAML2 基因重排与网织和复合血管内皮细胞瘤。
Am J Surg Pathol. 2020 Dec;44(12):1677-1684. doi: 10.1097/PAS.0000000000001575.
6
A case of retiform-hemangioendothelioma with unusual presentation and aggressive clinical features.一例具有不寻常表现和侵袭性临床特征的网状血管内皮瘤病例。
Int J Clin Exp Pathol. 2010 May 12;3(5):528-33.
7
Contributions of Dr. Juan Rosai to the pathology of cutaneous vascular proliferations: A review of selected lesions.胡安·罗萨伊博士对皮肤血管增生病理学的贡献:对部分病变的综述
Semin Diagn Pathol. 2016 Sep;33(5):284-93. doi: 10.1053/j.semdp.2016.05.010. Epub 2016 May 13.
8
The First Case of Composite Hemangioendothelioma in The Heart.首例心脏复合性血管内皮瘤病例。
Heart Surg Forum. 2022 Apr 22;25(2):E284-E287. doi: 10.1532/hsf.4587.
9
Cutaneous composite hemangioendothelioma with satellitosis and lymph node metastases.伴有卫星灶及淋巴结转移的皮肤复合性血管内皮瘤
J Cutan Pathol. 2008 Feb;35(2):225-30. doi: 10.1111/j.1600-0560.2007.00781.x.
10
Composite hemangioendothelioma: a complex, low-grade vascular lesion mimicking angiosarcoma.复合性血管内皮瘤:一种类似血管肉瘤的复杂低度血管性病变。
Am J Surg Pathol. 2000 Mar;24(3):352-61. doi: 10.1097/00000478-200003000-00003.

引用本文的文献

1
Composite hemangioendothelioma: report of a rare neoplasm.
An Bras Dermatol. 2025 Sep-Oct;100(5):501166. doi: 10.1016/j.abd.2025.501166. Epub 2025 Aug 9.
2
the enigma: composite hemangioendothelioma of the base of tongue-a comprehensive review of literature.谜团:舌根部复合性血管内皮瘤——文献综述
J Maxillofac Oral Surg. 2025 Jun;24(3):820-825. doi: 10.1007/s12663-025-02451-1. Epub 2025 Jan 23.
3
Recurrence-Free Survival in Composite Hemangioendothelioma: A Case Study and Updated Systematic Review.复合性血管内皮瘤的无复发生存率:一项病例研究及最新系统评价

本文引用的文献

1
Cutaneous composite hemangioendothelioma on the nose treated with electron beam.
Int J Dermatol. 2013 Dec;52(12):1618-9. doi: 10.1111/j.1365-4632.2011.05432.x. Epub 2012 Sep 24.
2
Composite haemangioendothelioma: report of four cases with emphasis on atypical clinical presentation.复合性血管内皮瘤:四例报告并着重于非典型临床表现
Pathology. 2011 Feb;43(2):176-80. doi: 10.1097/PAT.0b013e328342718d.
3
Composite haemangioendothelioma with lymph-node metastasis: an unusual presentation at an uncommon site.伴有淋巴结转移的复合性血管内皮细胞瘤:不常见部位的不常见表现。
J Clin Med. 2025 Apr 8;14(8):2541. doi: 10.3390/jcm14082541.
4
Dural composite hemangioendothelioma: The first intracranial case.硬脑膜复合性血管内皮瘤:首例颅内病例。
Surg Neurol Int. 2024 Feb 23;15:55. doi: 10.25259/SNI_3_2024. eCollection 2024.
5
Composite hemangioendothelioma- report of two cases located in bone and review of the literature.骨复合型血管内皮细胞瘤——两例报告及文献复习。
BMC Musculoskelet Disord. 2023 Aug 24;24(1):676. doi: 10.1186/s12891-023-06745-8.
6
Multiply Recurrent Composite Hemangioendothelioma of Penis with Histologic Progression to High-Grade Features.阴茎多发性复发性复合性血管内皮瘤伴组织学进展至高级别特征
Dermatopathology (Basel). 2023 Jan 11;10(1):41-45. doi: 10.3390/dermatopathology10010005.
7
Composite hemangioendothelioma in the cervical spine with kaposiform hemangioendothelioma features in an elderly patient: a case report.老年患者颈椎的复合性血管内皮细胞瘤伴kaposiform 血管内皮细胞瘤特征:病例报告。
BMC Geriatr. 2022 Dec 9;22(1):952. doi: 10.1186/s12877-022-03677-1.
8
Cutaneous Vascular Neoplasms of Uncertain Biological Behavior.生物学行为不确定的皮肤血管肿瘤
Biology (Basel). 2021 Nov 9;10(11):1160. doi: 10.3390/biology10111160.
9
Composite hemangioendothelioma with neuroendocrine marker expression: an aggressive variant.复合性血管内皮细胞瘤伴神经内分泌标志物表达:一种侵袭性变异型。
Mod Pathol. 2017 Nov;30(11):1589-1602. doi: 10.1038/modpathol.2017.83. Epub 2017 Jul 21.
Clin Exp Dermatol. 2009 Dec;34(8):e802-6. doi: 10.1111/j.1365-2230.2009.03529.x.
4
Composite cutaneous hemangioendothelioma on the back.
Am J Dermatopathol. 2008 Jun;30(3):262-4. doi: 10.1097/DAD.0b013e31816c3f8e.
5
Composite cutaneous haemangioendothelioma treated with interferon.用干扰素治疗的复合性皮肤血管内皮瘤
J Eur Acad Dermatol Venereol. 2008 Apr;22(4):503-5. doi: 10.1111/j.1468-3083.2007.02366.x.
6
Cutaneous composite hemangioendothelioma with satellitosis and lymph node metastases.伴有卫星灶及淋巴结转移的皮肤复合性血管内皮瘤
J Cutan Pathol. 2008 Feb;35(2):225-30. doi: 10.1111/j.1600-0560.2007.00781.x.
7
Composite hemangioendothelioma: report of 5 cases including one with associated Maffucci syndrome.复合性血管内皮瘤:5例报告,其中1例伴有马富西综合征。
Am J Surg Pathol. 2007 Oct;31(10):1567-72. doi: 10.1097/PAS.0b013e318038f6b5.
8
Spindle cell hemangioma and epithelioid hemangioendothelioma arising in an area of lymphedema.
Am J Dermatopathol. 2006 Jun;28(3):223-7. doi: 10.1097/00000372-200606000-00010.
9
Composite cutaneous haemangioendothelioma: case report and review of the literature.复合性皮肤血管内皮瘤:病例报告及文献综述
Clin Exp Dermatol. 2005 Jul;30(4):385-7. doi: 10.1111/j.1365-2230.2005.01786.x.
10
Congenital composite hemangioendothelioma: case report and reappraisal of the hemangioendothelioma spectrum.先天性复合性血管内皮瘤:病例报告及对血管内皮瘤谱系的重新评估
J Cutan Pathol. 2002 Apr;29(4):226-31. doi: 10.1034/j.1600-0560.2002.290405.x.