综合组织分子方法鉴别原发性头皮毛囊中心区和边缘区淋巴瘤。

IF 3 3区 医学 Q1 PATHOLOGY
Marie Donzel, Alexis Trecourt, Stéphane Dalle, Olivier Harou, Marie Perier-Muzet, Florent Grange, Brigitte Balme, Florian Pesce, Alexandra Traverse-Glehen, Claire Mauduit
{"title":"综合组织分子方法鉴别原发性头皮毛囊中心区和边缘区淋巴瘤。","authors":"Marie Donzel, Alexis Trecourt, Stéphane Dalle, Olivier Harou, Marie Perier-Muzet, Florent Grange, Brigitte Balme, Florian Pesce, Alexandra Traverse-Glehen, Claire Mauduit","doi":"10.1016/j.pathol.2025.04.009","DOIUrl":null,"url":null,"abstract":"<p><p>Overlapping features between follicular lymphomas (FLs) and marginal zone lymphomas (MZLs) have been described, especially in their paediatric forms. Although adult primary cutaneous follicle centre lymphoma (PCFL) and primary cutaneous marginal zone lymphoma (PCMZL) of the scalp appear to display overlapping histological and molecular features, these entities have never been studied. The aim of this study was to describe the clinical, histological, and mutational profiles of PCFL and PCMZL of the scalp and to highlight possible overlapping features. From 2011 to 2023, 38 patients with PCFL or PCMZL of the scalp from two centres were retrospectively included. In each case, a histological review, immunohistochemistry with additional immunostaining for myeloid cell nuclear differentiation antigen, BCL2 fluorescence in situ hybridisation, and targeted next-generation sequencing were performed. Among the 23 PCFL (60%) and 15 PCMZL (40%) cases included, 10 had a difficult initial diagnosis based on histological data alone. The most frequent pathogenic variants in PCFL cases were TNFRSF14 (15%), BCL2 (11%), SOCS1 (11%), and CREBBP (6%). The most frequent pathogenic variants in PCMZL cases were TNFAIP3 (24%), KMT2D (14%), CARD11 (10%), and ITPKB (10%). The integrated histomolecular approach helped reclassify five PCMZL cases into PCFL and showed plasmacytic differentiation in 12% of PCFL cases. This study highlights the histological and molecular overlaps between PCFL and PCMZL of the scalp and underscores the interest of an integrated histomolecular diagnosis to discriminate between these entities.</p>","PeriodicalId":19915,"journal":{"name":"Pathology","volume":" ","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2025-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Integrated histomolecular approach to discriminate primary cutaneous follicle centre and marginal zone lymphoma of the scalp.\",\"authors\":\"Marie Donzel, Alexis Trecourt, Stéphane Dalle, Olivier Harou, Marie Perier-Muzet, Florent Grange, Brigitte Balme, Florian Pesce, Alexandra Traverse-Glehen, Claire Mauduit\",\"doi\":\"10.1016/j.pathol.2025.04.009\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Overlapping features between follicular lymphomas (FLs) and marginal zone lymphomas (MZLs) have been described, especially in their paediatric forms. Although adult primary cutaneous follicle centre lymphoma (PCFL) and primary cutaneous marginal zone lymphoma (PCMZL) of the scalp appear to display overlapping histological and molecular features, these entities have never been studied. The aim of this study was to describe the clinical, histological, and mutational profiles of PCFL and PCMZL of the scalp and to highlight possible overlapping features. From 2011 to 2023, 38 patients with PCFL or PCMZL of the scalp from two centres were retrospectively included. In each case, a histological review, immunohistochemistry with additional immunostaining for myeloid cell nuclear differentiation antigen, BCL2 fluorescence in situ hybridisation, and targeted next-generation sequencing were performed. Among the 23 PCFL (60%) and 15 PCMZL (40%) cases included, 10 had a difficult initial diagnosis based on histological data alone. The most frequent pathogenic variants in PCFL cases were TNFRSF14 (15%), BCL2 (11%), SOCS1 (11%), and CREBBP (6%). The most frequent pathogenic variants in PCMZL cases were TNFAIP3 (24%), KMT2D (14%), CARD11 (10%), and ITPKB (10%). The integrated histomolecular approach helped reclassify five PCMZL cases into PCFL and showed plasmacytic differentiation in 12% of PCFL cases. This study highlights the histological and molecular overlaps between PCFL and PCMZL of the scalp and underscores the interest of an integrated histomolecular diagnosis to discriminate between these entities.</p>\",\"PeriodicalId\":19915,\"journal\":{\"name\":\"Pathology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2025-06-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pathology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.pathol.2025.04.009\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PATHOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pathology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.pathol.2025.04.009","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PATHOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

滤泡性淋巴瘤(FLs)和边缘区淋巴瘤(MZLs)之间的重叠特征已经被描述,特别是在他们的儿科形式。虽然头皮的成人原发性皮肤毛囊中心淋巴瘤(PCFL)和原发性皮肤边缘区淋巴瘤(PCMZL)似乎表现出重叠的组织学和分子特征,但这些实体从未被研究过。本研究的目的是描述头皮PCFL和PCMZL的临床、组织学和突变特征,并强调可能的重叠特征。从2011年到2023年,回顾性分析了来自两个中心的38例头皮PCFL或PCMZL患者。在每个病例中,都进行了组织学检查,免疫组织化学和额外的骨髓细胞核分化抗原免疫染色,BCL2荧光原位杂交,以及靶向下一代测序。在23例PCFL(60%)和15例PCMZL(40%)病例中,10例仅根据组织学资料难以进行初步诊断。PCFL病例中最常见的致病变异是TNFRSF14(15%)、BCL2(11%)、SOCS1(11%)和CREBBP(6%)。PCMZL病例中最常见的致病变异是TNFAIP3(24%)、KMT2D(14%)、CARD11(10%)和ITPKB(10%)。综合组织分子方法帮助将5例PCMZL重新分类为PCFL,并在12%的PCFL病例中显示浆细胞分化。本研究强调了头皮PCFL和PCMZL之间的组织学和分子重叠,并强调了综合组织分子诊断来区分这些实体的兴趣。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Integrated histomolecular approach to discriminate primary cutaneous follicle centre and marginal zone lymphoma of the scalp.

Overlapping features between follicular lymphomas (FLs) and marginal zone lymphomas (MZLs) have been described, especially in their paediatric forms. Although adult primary cutaneous follicle centre lymphoma (PCFL) and primary cutaneous marginal zone lymphoma (PCMZL) of the scalp appear to display overlapping histological and molecular features, these entities have never been studied. The aim of this study was to describe the clinical, histological, and mutational profiles of PCFL and PCMZL of the scalp and to highlight possible overlapping features. From 2011 to 2023, 38 patients with PCFL or PCMZL of the scalp from two centres were retrospectively included. In each case, a histological review, immunohistochemistry with additional immunostaining for myeloid cell nuclear differentiation antigen, BCL2 fluorescence in situ hybridisation, and targeted next-generation sequencing were performed. Among the 23 PCFL (60%) and 15 PCMZL (40%) cases included, 10 had a difficult initial diagnosis based on histological data alone. The most frequent pathogenic variants in PCFL cases were TNFRSF14 (15%), BCL2 (11%), SOCS1 (11%), and CREBBP (6%). The most frequent pathogenic variants in PCMZL cases were TNFAIP3 (24%), KMT2D (14%), CARD11 (10%), and ITPKB (10%). The integrated histomolecular approach helped reclassify five PCMZL cases into PCFL and showed plasmacytic differentiation in 12% of PCFL cases. This study highlights the histological and molecular overlaps between PCFL and PCMZL of the scalp and underscores the interest of an integrated histomolecular diagnosis to discriminate between these entities.

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
Pathology
Pathology 医学-病理学
CiteScore
6.50
自引率
2.20%
发文量
459
审稿时长
54 days
期刊介绍: Published by Elsevier from 2016 Pathology is the official journal of the Royal College of Pathologists of Australasia (RCPA). It is committed to publishing peer-reviewed, original articles related to the science of pathology in its broadest sense, including anatomical pathology, chemical pathology and biochemistry, cytopathology, experimental pathology, forensic pathology and morbid anatomy, genetics, haematology, immunology and immunopathology, microbiology and molecular pathology.
×
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:604180095
Book学术官方微信