Evidence map›Paper›PMID 42294335›Full record

ArticleFrontiers in oncology2026

Primary central nervous system lymphoma and tumefactive demyelinating lesions in multiple sclerosis: a retrospective observational cohort study.

Yushan Chen, Lvying Shen, Shaoqiang Chen, Shunyong Zheng, Jianmin Xie, Shuishun Zheng

Abstract read
In one paragraph

Article in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yushan Chen *Radiology Department, Zhangzhou Affiliated Hospital of Fujian Medical University, Zhangzhou, Fujian, China.
Lvying Shen *Hematology Department, Zhangzhou Affiliated Hospital of Fujian Medical University, Zhangzhou, Fujian, China.
Shaoqiang ChenDepartment of Human Anatomy, Fujian Medical University, Fuzhou, China.
Shunyong ZhengDepartment of Imaging, Zhangzhou Affiliated Hospital of Fujian Medical University, Zhangzhou, China.
Jianmin XieNeurosurgery Department, Fujian Zhangzhou Traditional Chinese Medicine Hospital, Zhangzhou, Fujian, China.
Shuishun ZhengNeurosurgery Department, Zhangzhou Affiliated Hospital of Fujian Medical University, Zhangzhou, Fujian, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Differentiating primary central nervous system lymphoma (PCNSL) from tumefactive demyelinating lesions (TDLs) remains a major diagnostic challenge. Objective: Our study aimed to compare the differences in clinical observations, neuroimaging data, and pathological features between the PCNSL and TDLs, as well as their potential biomarkers. Method: This was a retrospective observational cohort study of 183 patients (97 PCNSL and 86 TDLs). Baseline clinical data were collected. Neuroimaging features were determined by MRI. Pathological characteristics were evaluated by using hematoxylin-eosin (HE) staining, and immunochemical staining of CD3 and CD20. Cerebrospinal fluid (CSF) and serum biomarkers were detected by using the commercial protein assay kit and the enzyme-linked immunosorbent assay. Results: Patients with PCNSL had an older onset age, with the mean age being 59 ± 10 years in the PCNSL group and 36 ± 8 years in the TDL group (p < 0.001). Upon MRI scans, brain lesions in PCNSL showed U-shaped hyperintense, while lesions in TDLs showed slightly diffuse hyperintense on diffusion-weighted imaging (DWI) sequence. PCNSL lesions showed obvious hyperintense and perifocal edema, while TDL lesions showed isointense with partial perifocal edema on fluid attenuated inversion recovery (FLAIR) sequences. CD20 was strongly positive, while CD3 was negative in PCNSL tissues, which was different from a lower CD20 and stronger CD3 levels in TDLs. IL-6 and IL-10 levels was higher in the CSF of PCNSL than TDLs. Conclusion: Careful and comprehensive evaluation of clinical, neuroimaging, and pathological features, and CSF IL-6 and IL-10 levels facilitates the differential diagnosis betweenPCNSL and TDLs.

Indexed as

diagnosisneuroimagingpathologyprimary central nervous system lymphomatumefactive demyelinating lesions

Identifiers

PMID42294335
PMCPMC13260794

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.