Evidence map›Paper›PMID 41565277›Full record

ArticleJournal of clinical and experimental hematopathology : JCEH2026

Primary gastric EBV-positive cytotoxic-molecule-negative T-cell lymphoma with TET2 multihit mutations: a case report.

Masako Kurashige, Akihisa Hino, Koki Muto, Keisuke Nagahama, Takehiro Yamamoto, Keiichi Nakata, Michiko Ichii, Kentaro Fukushima, Kennosuke Karube, Yasuhito Nannya and 3 more

Abstract readCase Reports
In one paragraph

Article in Journal of clinical and experimental hematopathology : JCEH, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Masako KurashigeDepartment of Pathology, Graduate School of Medicine, The University of Osaka, Suita, Osaka, Japan.
Akihisa HinoDepartment of Hematology and Oncology, Graduate School of Medicine, The University of Osaka, Suita, Osaka, Japan.
Koki MutoDepartment of Pathology, Graduate School of Medicine, The University of Osaka, Suita, Osaka, Japan.
Keisuke NagahamaDepartment of Hematology and Oncology, Graduate School of Medicine, The University of Osaka, Suita, Osaka, Japan.
Takehiro YamamotoDepartment of Pathology, Graduate School of Medicine, The University of Osaka, Suita, Osaka, Japan.
Keiichi NakataDepartment of Hematology, Suita Municipal Hospital, Suita, Osaka, Japan.
Michiko IchiiDepartment of Hematology and Oncology, Graduate School of Medicine, The University of Osaka, Suita, Osaka, Japan.
Kentaro FukushimaDepartment of Hematology and Oncology, Graduate School of Medicine, The University of Osaka, Suita, Osaka, Japan.
Kennosuke KarubeDepartment of Pathology and Laboratory Medicine, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Yasuhito NannyaDivision of Hematopoietic Disease Control, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Naoki HosenDepartment of Hematology and Oncology, Graduate School of Medicine, The University of Osaka, Suita, Osaka, Japan.
Seishi OgawaDepartment of Pathology and Tumor Biology, Kyoto University, Kyoto, Japan.
Eiichi MoriiDepartment of Pathology, Graduate School of Medicine, The University of Osaka, Suita, Osaka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extranodal NK/T-cell lymphoma (ENKTL) is an Epstein-Barr virus (EBV)-positive lymphoma of the NK- or cytotoxic T-cell lineage. According to the World Health Organization Classification of Hematolymphoid Tumors, Fifth Edition (WHO-HAEM5), EBV-positive cases lacking cytotoxic molecules cannot be classified as ENKTL. To the best of our knowledge, this is the first documented case of primary gastric EBV-positive T-cell lymphoma lacking the expression of cytotoxic molecules. A 76-year-old woman initially presented with a disease confined to the stomach, with subsequent contiguous extension into the duodenum. Biopsies revealed small- to medium-sized atypical T cells with pale cytoplasm and irregularly folded nuclei, as well as intravascular infiltration. Tumor cells were positive for CD3, TCRβF1, and CD4 and negative for CD56, TIA-1, granzyme B, perforin, and PD-L1. EBV-encoded RNA in situ hybridization highlighted neoplastic T cells. These findings did not fulfill the criteria for any T/NK cell entity of WHO-HAEM5 including ENKTL and peripheral T-cell lymphoma not otherwise specified (PTCL, NOS). Targeted sequencing revealed TET2 multihit mutations, suggesting clonal hematopoiesis-linked pathogenesis. Given the patient's age and tumor location, we administered a reduced dose of DeVIC, followed by radiotherapy, achieving partial remission. This case expands the spectrum of EBV-associated T-cell lymphomas and highlights the need for additional cases to refine the classification and management.

Indexed as

DNA-Binding ProteinsEpstein-Barr Virus InfectionsHerpesvirus 4, HumanLymphoma, T-CellMutationProto-Oncogene ProteinsStomach NeoplasmsAgedDioxygenasesFemaleHumansDioxygenasesDNA-Binding ProteinsProto-Oncogene ProteinsTET2 protein, humanclonal hematopoiesiscytotoxic molecule–negativeEpstein–Barr virusgastric T-cell lymphomaTET2 multihit mutations

Identifiers

PMID41565277
PMCPMC13160649

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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.