新出现的“颅内”间充质肿瘤的颅外中枢神经系统表现,FET: creb融合阳性。

IF 2.7 3区 医学 Q2 CLINICAL NEUROLOGY
Arnault Tauziède-Espariat, Gaëlle Pierron, Delphine Guillemot, Chiara Benevello, Johan Pallud, Joseph Benzakoun, Lauren Hasty, Alice Métais, Fabrice Chrétien, Pascale Varlet
{"title":"新出现的“颅内”间充质肿瘤的颅外中枢神经系统表现,FET: creb融合阳性。","authors":"Arnault Tauziède-Espariat,&nbsp;Gaëlle Pierron,&nbsp;Delphine Guillemot,&nbsp;Chiara Benevello,&nbsp;Johan Pallud,&nbsp;Joseph Benzakoun,&nbsp;Lauren Hasty,&nbsp;Alice Métais,&nbsp;Fabrice Chrétien,&nbsp;Pascale Varlet","doi":"10.1007/s10014-022-00443-4","DOIUrl":null,"url":null,"abstract":"<p><p>A novel histomolecular tumor, the \"intracranial mesenchymal tumor (IMT), FET::CREB fusion-positive\", has recently been identified and added to the 2021 World Health Organization Classification of Tumors of the Central Nervous System. One of the essential diagnostic criteria defined in this classification is the intracranial location of the tumor. Herein, we report a spinal case of IMT with a classical EWSR1::CREM fusion. We compare its clinical, histopathological, immunophenotypical, genetic and epigenetic features with those previously described in IMT, FET::CREB fusion-positive. The current case presented histopathological (epithelioid morphology with mucin-rich stroma, and expression of EMA and desmin), radiological (an extraparenchymal lobulated mass without dural tail), genetic (fusion implicating the EWSR1 and CREM genes), and epigenetic (DNA-methylation profiling) similarities to previously reported cases. This case constitutes the third \"extracranial\" observation of an IMT. Our results added data suggesting that the terminology \"IMT, FET::CREB fusion-positive\" is provisional and that further series of cases are needed to better characterize them.</p>","PeriodicalId":9226,"journal":{"name":"Brain Tumor Pathology","volume":"40 1","pages":"35-39"},"PeriodicalIF":2.7000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"An extracranial CNS presentation of the emerging \\\"intracranial\\\" mesenchymal tumor, FET: CREB-fusion positive.\",\"authors\":\"Arnault Tauziède-Espariat,&nbsp;Gaëlle Pierron,&nbsp;Delphine Guillemot,&nbsp;Chiara Benevello,&nbsp;Johan Pallud,&nbsp;Joseph Benzakoun,&nbsp;Lauren Hasty,&nbsp;Alice Métais,&nbsp;Fabrice Chrétien,&nbsp;Pascale Varlet\",\"doi\":\"10.1007/s10014-022-00443-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A novel histomolecular tumor, the \\\"intracranial mesenchymal tumor (IMT), FET::CREB fusion-positive\\\", has recently been identified and added to the 2021 World Health Organization Classification of Tumors of the Central Nervous System. One of the essential diagnostic criteria defined in this classification is the intracranial location of the tumor. Herein, we report a spinal case of IMT with a classical EWSR1::CREM fusion. We compare its clinical, histopathological, immunophenotypical, genetic and epigenetic features with those previously described in IMT, FET::CREB fusion-positive. The current case presented histopathological (epithelioid morphology with mucin-rich stroma, and expression of EMA and desmin), radiological (an extraparenchymal lobulated mass without dural tail), genetic (fusion implicating the EWSR1 and CREM genes), and epigenetic (DNA-methylation profiling) similarities to previously reported cases. This case constitutes the third \\\"extracranial\\\" observation of an IMT. Our results added data suggesting that the terminology \\\"IMT, FET::CREB fusion-positive\\\" is provisional and that further series of cases are needed to better characterize them.</p>\",\"PeriodicalId\":9226,\"journal\":{\"name\":\"Brain Tumor Pathology\",\"volume\":\"40 1\",\"pages\":\"35-39\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Brain Tumor Pathology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s10014-022-00443-4\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain Tumor Pathology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s10014-022-00443-4","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 1

摘要

最近发现了一种新的组织分子肿瘤“颅内间充质瘤(IMT), FET::CREB融合阳性”,并将其添加到2021年世界卫生组织中枢神经系统肿瘤分类中。在这种分类中定义的基本诊断标准之一是肿瘤的颅内位置。在此,我们报告一例脊柱IMT合并经典EWSR1::CREM融合。我们将其临床、组织病理学、免疫表型、遗传和表观遗传特征与先前描述的IMT、FET::CREB融合阳性进行比较。目前的病例在组织病理学上(上皮样形态,有富含黏液的基质,EMA和desmin的表达)、放射学上(没有硬脑膜尾的肝实质外分叶状肿块)、遗传学上(融合了EWSR1和CREM基因)和表观遗传学上(dna甲基化谱)与先前报道的病例相似。本病例是第三例IMT的“颅外”观察。我们的结果增加了数据,表明术语“IMT, FET::CREB融合阳性”是暂时的,需要进一步的病例系列来更好地表征它们。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

An extracranial CNS presentation of the emerging "intracranial" mesenchymal tumor, FET: CREB-fusion positive.

An extracranial CNS presentation of the emerging "intracranial" mesenchymal tumor, FET: CREB-fusion positive.

A novel histomolecular tumor, the "intracranial mesenchymal tumor (IMT), FET::CREB fusion-positive", has recently been identified and added to the 2021 World Health Organization Classification of Tumors of the Central Nervous System. One of the essential diagnostic criteria defined in this classification is the intracranial location of the tumor. Herein, we report a spinal case of IMT with a classical EWSR1::CREM fusion. We compare its clinical, histopathological, immunophenotypical, genetic and epigenetic features with those previously described in IMT, FET::CREB fusion-positive. The current case presented histopathological (epithelioid morphology with mucin-rich stroma, and expression of EMA and desmin), radiological (an extraparenchymal lobulated mass without dural tail), genetic (fusion implicating the EWSR1 and CREM genes), and epigenetic (DNA-methylation profiling) similarities to previously reported cases. This case constitutes the third "extracranial" observation of an IMT. Our results added data suggesting that the terminology "IMT, FET::CREB fusion-positive" is provisional and that further series of cases are needed to better characterize them.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Brain Tumor Pathology
Brain Tumor Pathology 医学-病理学
CiteScore
5.40
自引率
9.10%
发文量
30
审稿时长
>12 weeks
期刊介绍: Brain Tumor Pathology is the official journal of the Japan Society of Brain Tumor Pathology. This international journal documents the latest research and topical debate in all clinical and experimental fields relating to brain tumors, especially brain tumor pathology. The journal has been published since 1983 and has been recognized worldwide as a unique journal of high quality. The journal welcomes the submission of manuscripts from any country. Membership in the society is not a prerequisite for submission. The journal publishes original articles, case reports, rapid short communications, instructional lectures, review articles, letters to the editor, and topics.Review articles and Topics may be recommended at the annual meeting of the Japan Society of Brain Tumor Pathology. All contributions should be aimed at promoting international scientific collaboration.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信