Clinicopathological analysis of primary central nervous system lymphoma in patients with or without HIV infection

IF 1.5 4区 医学 Q3 PATHOLOGY
Man Li , Jiamin Chen , Peng Wang , Enshan Feng , Xiangmei Chen , Haili Gao , Zhiyuan Ma , Xingang Zhou
{"title":"Clinicopathological analysis of primary central nervous system lymphoma in patients with or without HIV infection","authors":"Man Li ,&nbsp;Jiamin Chen ,&nbsp;Peng Wang ,&nbsp;Enshan Feng ,&nbsp;Xiangmei Chen ,&nbsp;Haili Gao ,&nbsp;Zhiyuan Ma ,&nbsp;Xingang Zhou","doi":"10.1016/j.anndiagpath.2024.152383","DOIUrl":null,"url":null,"abstract":"<div><div>The clinicopathological features of HIV-related primary central nervous system lymphoma (PCNSL) and immunocompetent primary central nervous system lymphoma (IC-PCNSL) were found to be distinct. Thirty-seven patients with HIV-related PCNSL and thirty patients with IC-PCNSL were included in our study. Hematoxylin &amp; eosin (HE) staining, immunohistochemical detection using CD10, MUM1, CD20, Bcl-2, Bcl-6, p53, C-MYC, Ki67, methyltransferase like factor 3 (METTL3) antibodies and Epstein–Barr encoding region (EBER) in situ hybridization were performed. All of the patients were classified as the diffuse large B-cell lymphoma (DLBCL) histological type. Patients with HIV-related PCNSL were younger and more likely to be male, with elevated lactate dehydrogenase (LDH) and low sugar content in cerebrospinal fluid (CSF) compared to patients with IC-PCNSL.The positive rates of METTL3, Bcl-2, p53 and EBER were significantly higher in HIV-related PCNSL patients than in IC-PCNSL patients. Furthermore, we also found that the expression of METTL3 was lower in germinal centre B-cell (GCB)-like DLBCL (<em>n</em> = 7) than in non-GCB like DLBCL (<em>n</em> = 30) in HIV-related PCNSL (<em>P</em> = 0.030); however, in IC-PCNSL patients, the expression of METTL3 was not significantly different between GCB-like DLBCL and non-GCB-like DLBCL (<em>P</em> = 0.670). Although the manifestations are similar in PCNSL patients with and without HIV, HIV-related PCNSL differs from IC-PCNSL in terms of pathological characteristics including METTL3, Bcl-2, p53 and EBER. We therefore suggest that the pathogenesis of HIV-related PCNSL and IC-PCNSL may differ according to host immune status.</div></div>","PeriodicalId":50768,"journal":{"name":"Annals of Diagnostic Pathology","volume":"73 ","pages":"Article 152383"},"PeriodicalIF":1.5000,"publicationDate":"2024-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Diagnostic Pathology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1092913424001205","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PATHOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The clinicopathological features of HIV-related primary central nervous system lymphoma (PCNSL) and immunocompetent primary central nervous system lymphoma (IC-PCNSL) were found to be distinct. Thirty-seven patients with HIV-related PCNSL and thirty patients with IC-PCNSL were included in our study. Hematoxylin & eosin (HE) staining, immunohistochemical detection using CD10, MUM1, CD20, Bcl-2, Bcl-6, p53, C-MYC, Ki67, methyltransferase like factor 3 (METTL3) antibodies and Epstein–Barr encoding region (EBER) in situ hybridization were performed. All of the patients were classified as the diffuse large B-cell lymphoma (DLBCL) histological type. Patients with HIV-related PCNSL were younger and more likely to be male, with elevated lactate dehydrogenase (LDH) and low sugar content in cerebrospinal fluid (CSF) compared to patients with IC-PCNSL.The positive rates of METTL3, Bcl-2, p53 and EBER were significantly higher in HIV-related PCNSL patients than in IC-PCNSL patients. Furthermore, we also found that the expression of METTL3 was lower in germinal centre B-cell (GCB)-like DLBCL (n = 7) than in non-GCB like DLBCL (n = 30) in HIV-related PCNSL (P = 0.030); however, in IC-PCNSL patients, the expression of METTL3 was not significantly different between GCB-like DLBCL and non-GCB-like DLBCL (P = 0.670). Although the manifestations are similar in PCNSL patients with and without HIV, HIV-related PCNSL differs from IC-PCNSL in terms of pathological characteristics including METTL3, Bcl-2, p53 and EBER. We therefore suggest that the pathogenesis of HIV-related PCNSL and IC-PCNSL may differ according to host immune status.
感染或未感染艾滋病毒患者原发性中枢神经系统淋巴瘤的临床病理分析
研究发现,HIV相关原发性中枢神经系统淋巴瘤(PCNSL)和免疫功能正常原发性中枢神经系统淋巴瘤(IC-PCNSL)的临床病理特征截然不同。我们的研究纳入了 37 例 HIV 相关 PCNSL 患者和 30 例 IC-PCNSL 患者。研究人员对患者进行了血沉和伊红(HE)染色,使用 CD10、MUM1、CD20、Bcl-2、Bcl-6、p53、C-MYC、Ki67、甲基转移酶样因子 3(METTL3)抗体进行了免疫组化检测,并进行了 Epstein-Barr 编码区(EBER)原位杂交。所有患者均被归类为弥漫大B细胞淋巴瘤(DLBCL)组织学类型。与IC-PCNSL患者相比,HIV相关PCNSL患者更年轻,更可能是男性,乳酸脱氢酶(LDH)升高,脑脊液(CSF)中糖含量低。此外,我们还发现,在HIV相关PCNSL患者中,生殖中心B细胞(GCB)样DLBCL(n = 7)的METTL3表达低于非GCB样DLBCL(n = 30)(P = 0.030);但在IC-PCNSL患者中,GCB样DLBCL和非GCB样DLBCL的METTL3表达无明显差异(P = 0.670)。虽然感染和未感染艾滋病毒的 PCNSL 患者表现相似,但艾滋病毒相关 PCNSL 在病理特征(包括 METTL3、Bcl-2、p53 和 EBER)方面与 IC-PCNSL 不同。因此,我们认为,HIV 相关 PCNSL 和 IC-PCNSL 的发病机制可能因宿主免疫状态而异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
3.90
自引率
5.00%
发文量
149
审稿时长
26 days
期刊介绍: A peer-reviewed journal devoted to the publication of articles dealing with traditional morphologic studies using standard diagnostic techniques and stressing clinicopathological correlations and scientific observation of relevance to the daily practice of pathology. Special features include pathologic-radiologic correlations and pathologic-cytologic correlations.
×
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