Plasmablastic Lymphoma Associated with Adjacent Mature Plasma Cell Population Exhibiting Opposite Light Chain Restriction.

IF 0.7 Q4 PATHOLOGY
Case Reports in Pathology Pub Date : 2020-12-28 eCollection Date: 2020-01-01 DOI:10.1155/2020/8875547
Karina Furlan, Ira Miller, Brett Mahon, Fernando A Ocampo Gonzalez, Nicholas Ward
{"title":"Plasmablastic Lymphoma Associated with Adjacent Mature Plasma Cell Population Exhibiting Opposite Light Chain Restriction.","authors":"Karina Furlan,&nbsp;Ira Miller,&nbsp;Brett Mahon,&nbsp;Fernando A Ocampo Gonzalez,&nbsp;Nicholas Ward","doi":"10.1155/2020/8875547","DOIUrl":null,"url":null,"abstract":"<p><p>Plasmablastic lymphoma (PBL) is an aggressive high-grade B cell lymphoma, considered a variant of diffuse large B cell lymphoma with approximately 75% mortality within 6-7 months. We describe an unusual case of PBL arising as a maxillary mass in an HIV-negative, nontransplanted 78-year-old female. Histologic examination revealed a diffuse infiltrate of anaplastic appearing cells exhibiting plasmablastic morphology with an adjacent contiguous infiltrate of mature appearing plasma cells. The PBL and mature plasma cell components both demonstrated an immunophenotype of CD20(-), CD38(+), and CD138(+). The two populations differed by the PBL featuring a high proliferation rate by Ki-67 (~95%) with coexpression of both c-MYC and EBV, while the mature plasma cell component featured a low proliferation rate by Ki-67 (~5%) without coexpression of c-MYC or EBV. Kappa/lambda staining demonstrated lambda light chain restriction involving the PBL, while the mature plasma cell infiltrate revealed kappa light chain restriction. Our findings describe the rare association of PBL with a synchronous distinct population of mature plasma cells exhibiting opposite light chain restriction.</p>","PeriodicalId":45638,"journal":{"name":"Case Reports in Pathology","volume":"2020 ","pages":"8875547"},"PeriodicalIF":0.7000,"publicationDate":"2020-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803171/pdf/","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Pathology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2020/8875547","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2020/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"PATHOLOGY","Score":null,"Total":0}
引用次数: 1

Abstract

Plasmablastic lymphoma (PBL) is an aggressive high-grade B cell lymphoma, considered a variant of diffuse large B cell lymphoma with approximately 75% mortality within 6-7 months. We describe an unusual case of PBL arising as a maxillary mass in an HIV-negative, nontransplanted 78-year-old female. Histologic examination revealed a diffuse infiltrate of anaplastic appearing cells exhibiting plasmablastic morphology with an adjacent contiguous infiltrate of mature appearing plasma cells. The PBL and mature plasma cell components both demonstrated an immunophenotype of CD20(-), CD38(+), and CD138(+). The two populations differed by the PBL featuring a high proliferation rate by Ki-67 (~95%) with coexpression of both c-MYC and EBV, while the mature plasma cell component featured a low proliferation rate by Ki-67 (~5%) without coexpression of c-MYC or EBV. Kappa/lambda staining demonstrated lambda light chain restriction involving the PBL, while the mature plasma cell infiltrate revealed kappa light chain restriction. Our findings describe the rare association of PBL with a synchronous distinct population of mature plasma cells exhibiting opposite light chain restriction.

Abstract Image

Abstract Image

Abstract Image

浆母细胞淋巴瘤与邻近成熟浆细胞群表现相反轻链限制相关。
浆母细胞淋巴瘤(PBL)是一种侵袭性高级别B细胞淋巴瘤,被认为是弥漫性大B细胞淋巴瘤的一种变体,在6-7个月内死亡率约为75%。我们描述了一个不寻常的病例PBL引起的上颌肿块在一个hiv阴性,未移植的78岁女性。组织学检查显示弥漫性浸润的未分化细胞表现为浆细胞形态,并伴有相邻的成熟浆细胞浸润。PBL和成熟浆细胞成分均表现出CD20(-)、CD38(+)和CD138(+)的免疫表型。这两个群体的不同之处是,在同时表达c-MYC和EBV的情况下,PBL的Ki-67增殖率高(~95%),而成熟浆细胞组分的Ki-67增殖率低(~5%),不同时表达c-MYC和EBV。Kappa/lambda染色显示涉及PBL的lambda轻链限制,而成熟浆细胞浸润显示Kappa轻链限制。我们的研究结果描述了PBL与表现相反轻链限制的同步不同成熟浆细胞群的罕见关联。
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
自引率
0.00%
发文量
20
审稿时长
12 weeks
×
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