• 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

伴有罕见融合基因的骨假肌源性血管内皮瘤:病例报告及文献复习

Pseudomyogenic hemangioendothelioma of bone with rare fusion gene: Case report and literature review.

作者信息

Murshed Khaled A, Torres-Mora Jorge, ElSayed Ahmed Mounir, Ammar Adham, Al-Bozom Issam

机构信息

Department of Laboratory Medicine & Pathology Hamad Medical Corporation Doha Qatar.

Mayo Clinic Laboratories- Rochester Main Campus Rochester MN USA.

出版信息

Clin Case Rep. 2021 Jan 19;9(3):1494-1499. doi: 10.1002/ccr3.3808. eCollection 2021 Mar.

DOI:10.1002/ccr3.3808
PMID:33768875
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7981765/
Abstract

Pseudomyogenic hemangioendothelioma rarely arises in bone. fusion gene is rarely reported in PMHE of bone. Currently, fusion genes can be used as diagnostic markers in PMHE; however, their prognostic and therapeutic significance is unclear.

摘要

假性肌源性血管内皮瘤很少发生于骨。骨假性肌源性血管内皮瘤中很少报道有融合基因。目前,融合基因可作为假性肌源性血管内皮瘤的诊断标志物;然而,它们的预后和治疗意义尚不清楚。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d2a/7981765/4852e4255bd1/CCR3-9-1494-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d2a/7981765/a50ed794b928/CCR3-9-1494-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d2a/7981765/630b9409a2d6/CCR3-9-1494-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d2a/7981765/3eec7fc67e66/CCR3-9-1494-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d2a/7981765/4852e4255bd1/CCR3-9-1494-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d2a/7981765/a50ed794b928/CCR3-9-1494-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d2a/7981765/630b9409a2d6/CCR3-9-1494-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d2a/7981765/3eec7fc67e66/CCR3-9-1494-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d2a/7981765/4852e4255bd1/CCR3-9-1494-g001.jpg

相似文献

1
Pseudomyogenic hemangioendothelioma of bone with rare fusion gene: Case report and literature review.伴有罕见融合基因的骨假肌源性血管内皮瘤:病例报告及文献复习
Clin Case Rep. 2021 Jan 19;9(3):1494-1499. doi: 10.1002/ccr3.3808. eCollection 2021 Mar.
2
Fusion of the Genes and in Pseudomyogenic Hemangioendothelioma.融合基因和在假性肌源性血管内皮瘤中的融合。
Cancer Genomics Proteomics. 2019 Jul-Aug;16(4):293-298. doi: 10.21873/cgp.20134.
3
Molecularly Confirmed Pseudomyogenic Hemangioendothelioma with Unusual EGFL7::FOSB Fusion in the Head and Neck Region of an Older Patient.分子确诊的假性肌源性血管内皮瘤伴不寻常的EGFL7::FOSB融合,发生于一名老年患者的头颈部区域。
Diagnostics (Basel). 2024 Feb 5;14(3):342. doi: 10.3390/diagnostics14030342.
4
A novel CLTC-FOSB gene fusion in pseudomyogenic hemangioendothelioma of bone.骨假肌样血管内皮瘤中存在新型 CLTC-FOSB 基因融合。
Genes Chromosomes Cancer. 2021 Jan;60(1):38-42. doi: 10.1002/gcc.22891. Epub 2020 Aug 22.
5
FOSB is a Useful Diagnostic Marker for Pseudomyogenic Hemangioendothelioma.FOSB是假性肌源性血管内皮瘤的一种有用诊断标志物。
Am J Surg Pathol. 2017 May;41(5):596-606. doi: 10.1097/PAS.0000000000000795.
6
Penile pseudomyogenic hemangioendothelioma/epithelioid sarcoma-like hemangioendothelioma with a novel pattern of SERPINE1-FOSB fusion detected by RT-PCR--report of a case.阴茎假肌源性血管内皮瘤/上皮样肉瘤样血管内皮瘤,通过逆转录聚合酶链反应检测到一种新的丝氨酸蛋白酶抑制剂E1- FBJ原癌基因FosB融合模式——病例报告
Pathol Res Pract. 2015 May;211(5):415-20. doi: 10.1016/j.prp.2015.02.003. Epub 2015 Feb 17.
7
The clinicopathological spectrum of pseudomyogenic hemangioendothelioma: report of an additional series with review of the literature.假肌源性血管内皮瘤的临床病理谱:附加系列报告并文献复习。
Virchows Arch. 2020 Aug;477(2):231-240. doi: 10.1007/s00428-020-02753-4. Epub 2020 Jan 24.
8
Pseudomyogenic hemangioendothelioma of bone treated with denosumab: a case report.骨假肌源性血管内皮瘤采用地舒单抗治疗:病例报告。
BMC Cancer. 2019 Sep 3;19(1):872. doi: 10.1186/s12885-019-6072-8.
9
Expanding the Spectrum of Genetic Alterations in Pseudomyogenic Hemangioendothelioma With Recurrent Novel ACTB-FOSB Gene Fusions.具有反复出现的新型 ACTB-FOSB 基因融合的假性肌源性血管内皮瘤中遗传改变谱的扩展。
Am J Surg Pathol. 2018 Dec;42(12):1653-1661. doi: 10.1097/PAS.0000000000001147.
10
A novel SERPINE1-FOSB fusion gene in pseudomyogenic hemangioendothelioma results in activation of intact FOSB and the PI3K-AKT-mTOR signaling pathway and responsiveness to sirolimus.在假性肌源性血管内皮瘤中发现一种新型 SERPINE1-FOSB 融合基因,导致完整的 FOSB 和 PI3K-AKT-mTOR 信号通路被激活,并对西罗莫司有反应。
J Dermatol. 2021 Dec;48(12):1900-1906. doi: 10.1111/1346-8138.16158. Epub 2021 Sep 27.

引用本文的文献

1
Pseudomyogenic hemangioendothelioma with bone and soft tissue involvement with favorable response to pamidronate: a case report and systematic review of the literature.骨及软组织受累的假肌源性血管内皮瘤对帕米膦酸盐治疗有效:病例报告及文献系统评价。
Arch Osteoporos. 2022 Feb 1;17(1):28. doi: 10.1007/s11657-022-01062-4.
2
The genetics of vascular tumours: an update.血管肿瘤的遗传学:更新。
Histopathology. 2022 Jan;80(1):19-32. doi: 10.1111/his.14458.

本文引用的文献

1
Multifocal Epithelioid Hemangioma of the Penis in a 4-Year-Old Child: A Case Report.
Am J Dermatopathol. 2020 May;42(5):372-374. doi: 10.1097/DAD.0000000000001566.
2
ZFP36-FOSB fusion in a haemorrhagic epithelioid and spindle cell haemangioma of bone: is there a family of FOSB-rearranged vascular neoplasms of the bone?骨出血性上皮样和梭形细胞血管瘤中的ZFP36-FOSB融合:是否存在一个FOSB重排的骨血管肿瘤家族?
Histopathology. 2020 Feb;76(3):490-493. doi: 10.1111/his.14002. Epub 2020 Jan 13.
3
Pseudomyogenic hemangioendothelioma of bone treated with denosumab: a case report.骨假肌源性血管内皮瘤采用地舒单抗治疗:病例报告。
BMC Cancer. 2019 Sep 3;19(1):872. doi: 10.1186/s12885-019-6072-8.
4
Pseudomyogenic hemangioendothelioma-A case report and review of the literature.假性肌源性血管内皮瘤——病例报告及文献综述
Radiol Case Rep. 2019 Aug 6;14(10):1228-1232. doi: 10.1016/j.radcr.2019.06.029. eCollection 2019 Oct.
5
Fusion of the Genes and in Pseudomyogenic Hemangioendothelioma.融合基因和在假性肌源性血管内皮瘤中的融合。
Cancer Genomics Proteomics. 2019 Jul-Aug;16(4):293-298. doi: 10.21873/cgp.20134.
6
Pseudomyogenic Hemangioendothelioma.假肌源性血管内皮瘤。
Arch Pathol Lab Med. 2019 Jun;143(6):763-767. doi: 10.5858/arpa.2017-0430-RS. Epub 2018 Dec 21.
7
Primary pseudomyogenic hemangioendothelioma of bone: case report and review of the literature.骨原发性假肌源性血管内皮瘤:病例报告及文献复习
Pathologica. 2018 Sep;110(2):96-101.
8
Diagnosis of known sarcoma fusions and novel fusion partners by targeted RNA sequencing with identification of a recurrent ACTB-FOSB fusion in pseudomyogenic hemangioendothelioma.通过靶向 RNA 测序诊断已知肉瘤融合基因和新型融合伙伴,并在假肌源性血管内皮瘤中鉴定出一种反复出现的 ACTB-FOSB 融合。
Mod Pathol. 2019 May;32(5):609-620. doi: 10.1038/s41379-018-0175-7. Epub 2018 Nov 21.
9
Expanding the Spectrum of Genetic Alterations in Pseudomyogenic Hemangioendothelioma With Recurrent Novel ACTB-FOSB Gene Fusions.具有反复出现的新型 ACTB-FOSB 基因融合的假性肌源性血管内皮瘤中遗传改变谱的扩展。
Am J Surg Pathol. 2018 Dec;42(12):1653-1661. doi: 10.1097/PAS.0000000000001147.
10
Pseudomyogenic hemangioendothelioma of skin, bone and soft tissue-a clinicopathological, immunohistochemical, and fluorescence in situ hybridization study.皮肤、骨和软组织的假肌源性血管内皮瘤:一项临床病理、免疫组织化学和荧光原位杂交研究。
Hum Pathol. 2018 Jan;71:126-134. doi: 10.1016/j.humpath.2017.10.023. Epub 2017 Nov 2.