• 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

MUC4 在血管肌纤维母细胞瘤中的表达。

MUC4 Expression in Angiomatoid Fibrous Histiocytoma.

机构信息

Bacchi Lab, Botucatu, SP, Brazil.

出版信息

Appl Immunohistochem Mol Morphol. 2020 Sep;28(8):641-645. doi: 10.1097/PAI.0000000000000816.

DOI:10.1097/PAI.0000000000000816
PMID:31652145
Abstract

Angiomatoid fibrous histiocytoma (AFH) is a rarely metastasizing neoplasm that typically occurs in the deep dermis and subcutis of the extremities of young patients, characterized by a t(2;22) translocation involving EWSR1 and CREB1. Because of its distinctive histologic features, the diagnosis of AFH is generally straightforward, although the immunohistochemistry (IHC) findings are relatively nonspecific. We recently encountered a case of primary cranial AFH that showed strong MUC4 IHC expression, which has not yet been reported previously. Prompted by this surprising finding, we investigated MUC4 expression in a series of AFH to evaluate this potential diagnostic pitfall. The expression of ALK by IHC, recently discovered in AFH, was also assessed in this study. We also analyzed EWSR1 rearrangement by fluorescence in situ hybridization using a dual color break-apart probe to confirm the diagnosis. The results showed MUC4 expression in 22.2% of AFH cases (4/18 cases), demonstrating a variable intensity of cytoplasmic staining. Most notably, one of the positive cases showed strong and diffuse expression. ALK IHC expression was observed in 17 of 18 cases (94.4%), usually in a diffuse and strong cytoplasmic pattern. EWSR1 rearrangement was demonstrated by fluorescence in situ hybridization in 81.2% of cases (13 of 16), including all the MUC4-positive cases. Our results indicate that although the significance of MUC4 expression in AFH is unknown, it is important to be aware that a subset of AFH can express the protein by IHC, expanding a variety of MUC4-positive mesenchymal tumors.

摘要

血管肌纤维母细胞瘤(angiomatoid fibrous histiocytoma,AFH)是一种罕见转移的肿瘤,通常发生在四肢的真皮和皮下组织深部,其特征在于涉及 EWSR1 和 CREB1 的 t(2;22)易位。由于其独特的组织学特征,AFH 的诊断通常较为直接,尽管免疫组织化学(immunohistochemistry,IHC)结果相对非特异性。我们最近遇到了一例原发于颅部的 AFH,其 MUC4 IHC 表达较强,此前尚未有报道。鉴于这一令人惊讶的发现,我们在一系列 AFH 中研究了 MUC4 的表达,以评估这一潜在的诊断陷阱。本研究还评估了最近在 AFH 中发现的 ALK 的 IHC 表达。我们还使用双色分离探针通过荧光原位杂交分析 EWSR1 重排,以确认诊断。结果显示,22.2%(4/18 例)的 AFH 病例表达 MUC4,表现为细胞质染色强度不同。最值得注意的是,其中一个阳性病例表现出强烈和弥漫的表达。18 例中有 17 例(94.4%)可见 ALK IHC 表达,通常呈弥漫和强细胞质模式。荧光原位杂交显示 81.2%(13/16 例)的病例存在 EWSR1 重排,包括所有 MUC4 阳性病例。我们的结果表明,尽管 MUC4 在 AFH 中的表达意义尚不清楚,但需要注意的是,AFH 中的一部分亚群可以通过 IHC 表达该蛋白,从而扩大了各种 MUC4 阳性间叶性肿瘤的范围。

相似文献

1
MUC4 Expression in Angiomatoid Fibrous Histiocytoma.MUC4 在血管肌纤维母细胞瘤中的表达。
Appl Immunohistochem Mol Morphol. 2020 Sep;28(8):641-645. doi: 10.1097/PAI.0000000000000816.
2
Angiomatoid fibrous histiocytoma: comparison of fluorescence in situ hybridization and reverse transcription polymerase chain reaction as adjunct diagnostic modalities.血管样纤维组织细胞瘤:荧光原位杂交与逆转录聚合酶链反应作为辅助诊断方法的比较
Ann Diagn Pathol. 2015 Jun;19(3):137-42. doi: 10.1016/j.anndiagpath.2015.03.004. Epub 2015 Mar 14.
3
ALK Expression in Angiomatoid Fibrous Histiocytoma: A Potential Diagnostic Pitfall.ALK 表达在血管肌纤维母细胞瘤中的表达:一个潜在的诊断陷阱。
Am J Surg Pathol. 2019 Jan;43(1):93-101. doi: 10.1097/PAS.0000000000001103.
4
MUC4 is a sensitive and extremely useful marker for sclerosing epithelioid fibrosarcoma: association with FUS gene rearrangement.MUC4 是硬化性上皮样纤维肉瘤的一个敏感且非常有用的标志物:与 FUS 基因重排相关。
Am J Surg Pathol. 2012 Oct;36(10):1444-51. doi: 10.1097/PAS.0b013e3182562bf8.
5
Intracranial mesenchymal tumor with FET-CREB fusion-A unifying diagnosis for the spectrum of intracranial myxoid mesenchymal tumors and angiomatoid fibrous histiocytoma-like neoplasms.颅内间质瘤伴 FET-CREB 融合——颅内黏液样间叶性肿瘤和血管外皮细胞瘤样肿瘤谱的统一诊断。
Brain Pathol. 2021 Jul;31(4):e12918. doi: 10.1111/bpa.12918. Epub 2021 Jan 28.
6
SOX9 Immunohistochemistry in the Distinction of Angiomatoid Fibrous Histiocytoma From Histologic Mimics: Diagnostic Utility and Pitfalls.SOX9 免疫组化在鉴别血管肌纤维母细胞瘤与组织学类似物中的作用:诊断效用及陷阱。
Appl Immunohistochem Mol Morphol. 2020 Sep;28(8):635-640. doi: 10.1097/PAI.0000000000000809.
7
Angiomatoid fibrous histiocytoma including cases with pleomorphic features analysed by fluorescence in situ hybridisation.血管肌纤维母细胞瘤包括通过荧光原位杂交分析的具有多形性特征的病例。
J Clin Pathol. 2010 Feb;63(2):124-8. doi: 10.1136/jcp.2009.072256.
8
Utility of FISH in the diagnosis of angiomatoid fibrous histiocytoma: a series of 18 cases.荧光原位杂交技术在血管肌纤维母细胞瘤诊断中的应用:18 例系列研究。
Mod Pathol. 2010 Jan;23(1):93-7. doi: 10.1038/modpathol.2009.138. Epub 2009 Oct 2.
9
Intracranial myxoid angiomatoid fibrous histiocytoma with "classic" histology and EWSR1:CREM fusion providing insight for reconciliation with intracranial myxoid mesenchymal tumors.具有“经典”组织学特征及EWSR1:CREM融合的颅内黏液样血管样纤维组织细胞瘤,为与颅内黏液样间叶性肿瘤的鉴别提供线索
Neuropathology. 2021 Aug;41(4):306-314. doi: 10.1111/neup.12737. Epub 2021 Jul 12.
10
Intracranial myxoid mesenchymal tumors with EWSR1-CREB family gene fusions: myxoid variant of angiomatoid fibrous histiocytoma or novel entity?颅内黏液样间叶性肿瘤伴 EWSR1-CREB 家族基因融合:血管外皮细胞瘤样纤维组织细胞瘤的黏液样变体还是新实体?
Brain Pathol. 2018 Mar;28(2):183-191. doi: 10.1111/bpa.12504. Epub 2017 Apr 11.

引用本文的文献

1
Extra-abdominal and intra-abdominal FET::CREM fusion mesenchymal neoplasms: comparative clinicopathological study of 9 new cases further supporting a distinct potentially aggressive sarcoma and report of novel sites.腹外和腹内FET::CREM融合间质性肿瘤:9例新病例的比较临床病理研究,进一步支持一种独特的潜在侵袭性肉瘤及新发病部位报告
Virchows Arch. 2024 Dec;485(6):1007-1019. doi: 10.1007/s00428-024-03917-2. Epub 2024 Sep 9.
2
An integrative histopathological and epigenetic characterization of primary intracranial mesenchymal tumors, FET:CREB-fused broadening the spectrum of tumor entities in comparison with their soft tissue counterparts.原发颅内间质瘤的综合组织病理学和表观遗传学特征,FET:CREB 融合——与软组织对应物相比,拓宽了肿瘤实体的范围。
Brain Pathol. 2022 Jan;32(1):e13010. doi: 10.1111/bpa.13010. Epub 2021 Jul 27.
3
MUC4 is expressed in alveolar rhabdomyosarcoma.MUC4 在肺泡横纹肌肉瘤中表达。
Histopathology. 2021 May;78(6):905-908. doi: 10.1111/his.14321. Epub 2021 Mar 16.
4
Distinct clinicopathological features of pulmonary primary angiomatoid fibrous histiocytoma: A report of four new cases and review of the literature.肺原发性血管外皮细胞瘤样纤维组织细胞瘤的独特临床病理特征:四例新病例报告及文献复习。
Thorac Cancer. 2021 Feb;12(3):314-323. doi: 10.1111/1759-7714.13727. Epub 2020 Dec 12.