Pathology for severe inflammatory PML with PD1/PD-L1 expression of favorable prognosis: What's a prognostic factor for PML-IRIS?

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY Neuropathology Pub Date : 2024-02-01 Epub Date: 2023-07-09 DOI:10.1111/neup.12929
Yukiko Shishido-Hara, Jiro Akimoto, Shinjiro Fukami, Michihiro Kohno, Jun Matsubayashi, Toshitaka Nagao
{"title":"Pathology for severe inflammatory PML with PD1/PD-L1 expression of favorable prognosis: What's a prognostic factor for PML-IRIS?","authors":"Yukiko Shishido-Hara, Jiro Akimoto, Shinjiro Fukami, Michihiro Kohno, Jun Matsubayashi, Toshitaka Nagao","doi":"10.1111/neup.12929","DOIUrl":null,"url":null,"abstract":"<p><p>A 72-year-old woman with dermatomyositis (DM) developed neurological manifestation, and magnetic resonance imaging (MRI) revealed multiple T2/fluid-attenuated inversion recovery (FLAIR)-hyperintense lesions predominantly in the deep white matter of the cerebral hemisphere. Punctate or linear contrast enhancement was observed surrounding the T1-hypointense area. Multiple T2/FLAIR-hyperintense lesions were aligned along with the corona radiata. Malignant lymphoma was first suspected, and a brain biopsy was performed. Pathological investigation suggested the provisional diagnosis of \"suspicious of malignant lymphoma.\" Owing to emergent clinical conditions, high-dose methotrexate (MTX) therapy was conducted, and then T2/FLAIR-hyperintense lesions were dramatically reduced. However, the diagnosis of malignant lymphoma was concerning since multiplex PCR demonstrated clonal restriction of the Ig H gene for B cells and TCR beta genes for T cells. Histopathology revealed the infiltration of both CD4<sup>+</sup> and CD8<sup>+</sup> T cells, and the CD4<sup>+</sup> /CD8<sup>+</sup> ratio was 4.0. Moreover, prominent plasma cells were observed, in addition to CD20<sup>+</sup> B cells. Atypical cells with enlarged nuclei were present, and they were not hematopoietic but found as glial cells. JC virus (JCV) infection was verified with both immunohistochemistry and in situ hybridization; the final diagnosis was progressive multifocal leukoencephalopathy (PML). The patient was treated with mefloquine and discharged. This case is informative in understanding the host anti-viral response. Variable inflammatory cells were observed, including CD4<sup>+</sup> and CD8<sup>+</sup> T cells, plasma cells, and a small amount of perivascular CD20<sup>+</sup> B cells. PD-1 and PD-L1 expression was observed in lymphoid cells and macrophages, respectively. PML with inflammatory reactions was thought fatal, and autopsy cases of PML with immune reconstitution inflammatory syndrome (IRIS) demonstrated excessive infiltration of only CD8<sup>+</sup> T cells. However, this case revealed infiltration of variable inflammatory cells, and a favorable prognosis would be expected under PD-1/PD-L1 immune-checkpoint regulation.</p>","PeriodicalId":19204,"journal":{"name":"Neuropathology","volume":" ","pages":"47-58"},"PeriodicalIF":1.3000,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuropathology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/neup.12929","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/7/9 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

A 72-year-old woman with dermatomyositis (DM) developed neurological manifestation, and magnetic resonance imaging (MRI) revealed multiple T2/fluid-attenuated inversion recovery (FLAIR)-hyperintense lesions predominantly in the deep white matter of the cerebral hemisphere. Punctate or linear contrast enhancement was observed surrounding the T1-hypointense area. Multiple T2/FLAIR-hyperintense lesions were aligned along with the corona radiata. Malignant lymphoma was first suspected, and a brain biopsy was performed. Pathological investigation suggested the provisional diagnosis of "suspicious of malignant lymphoma." Owing to emergent clinical conditions, high-dose methotrexate (MTX) therapy was conducted, and then T2/FLAIR-hyperintense lesions were dramatically reduced. However, the diagnosis of malignant lymphoma was concerning since multiplex PCR demonstrated clonal restriction of the Ig H gene for B cells and TCR beta genes for T cells. Histopathology revealed the infiltration of both CD4+ and CD8+ T cells, and the CD4+ /CD8+ ratio was 4.0. Moreover, prominent plasma cells were observed, in addition to CD20+ B cells. Atypical cells with enlarged nuclei were present, and they were not hematopoietic but found as glial cells. JC virus (JCV) infection was verified with both immunohistochemistry and in situ hybridization; the final diagnosis was progressive multifocal leukoencephalopathy (PML). The patient was treated with mefloquine and discharged. This case is informative in understanding the host anti-viral response. Variable inflammatory cells were observed, including CD4+ and CD8+ T cells, plasma cells, and a small amount of perivascular CD20+ B cells. PD-1 and PD-L1 expression was observed in lymphoid cells and macrophages, respectively. PML with inflammatory reactions was thought fatal, and autopsy cases of PML with immune reconstitution inflammatory syndrome (IRIS) demonstrated excessive infiltration of only CD8+ T cells. However, this case revealed infiltration of variable inflammatory cells, and a favorable prognosis would be expected under PD-1/PD-L1 immune-checkpoint regulation.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
重症炎性PML病理结果显示PD1/PD-L1表达预后良好:PML-IRIS的预后因素是什么?
一名72岁的皮肌炎(DM)女性患者出现了神经系统表现,磁共振成像(MRI)显示多发T2/流体增强反转恢复(FLAIR)高密度病变,主要位于大脑半球的深部白质。在T1高密度区周围观察到点状或线状对比增强。多个T2/FLAIR高密度病变与放射冠排列在一起。首先怀疑是恶性淋巴瘤,并进行了脑活检。病理检查提示临时诊断为 "疑似恶性淋巴瘤"。由于临床情况紧急,患者接受了大剂量甲氨蝶呤(MTX)治疗,T2/FLAIR高密度病灶明显缩小。然而,恶性淋巴瘤的诊断令人担忧,因为多重 PCR 显示 B 细胞的 Ig H 基因和 T 细胞的 TCR beta 基因存在克隆限制。组织病理学显示 CD4+ 和 CD8+ T 细胞均有浸润,CD4+/CD8+比率为 4.0。此外,除了 CD20+ B 细胞外,还观察到突出的浆细胞。出现了核增大的非典型细胞,它们不是造血细胞,而是胶质细胞。免疫组化和原位杂交验证了JC病毒(JCV)感染;最终诊断为进行性多灶性白质脑病(PML)。患者接受甲氟喹治疗后出院。该病例有助于了解宿主的抗病毒反应。观察到各种炎症细胞,包括 CD4+ 和 CD8+ T 细胞、浆细胞和少量血管周围 CD20+ B 细胞。在淋巴细胞和巨噬细胞中分别观察到 PD-1 和 PD-L1 的表达。伴有炎症反应的 PML 被认为是致命的,伴有免疫重建炎症综合征(IRIS)的 PML 尸检病例显示只有 CD8+ T 细胞过度浸润。然而,该病例显示了不同炎症细胞的浸润,在PD-1/PD-L1免疫检查点的调控下,预后良好。
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 去求助
来源期刊
Neuropathology
Neuropathology 医学-病理学
CiteScore
4.10
自引率
4.30%
发文量
105
审稿时长
6-12 weeks
期刊介绍: Neuropathology is an international journal sponsored by the Japanese Society of Neuropathology and publishes peer-reviewed original papers dealing with all aspects of human and experimental neuropathology and related fields of research. The Journal aims to promote the international exchange of results and encourages authors from all countries to submit papers in the following categories: Original Articles, Case Reports, Short Communications, Occasional Reviews, Editorials and Letters to the Editor. All articles are peer-reviewed by at least two researchers expert in the field of the submitted paper.
期刊最新文献
MYB::QKI fusion-positive diffuse glioma of the cerebellum: A case report. Utilizing quantitative susceptibility mapping to differentiate primary lateral sclerosis from progressive supranuclear palsy: A case report. Primary intracranial dedifferentiated liposarcoma: An extremely rare site with unusual histopathological findings. Solitary subependymal giant cell astrocytoma lacking TSC1/2 mutations and TTF-1 expression: A potential diagnostic pitfall. Adenoid glioblastoma: Stromal hypovascularity and secretion of chondromodulin-I by tumor cells.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1