Evidence map›Paper›PMID 39121027›Full record

ArticleAmerican journal of clinical pathology2025

Primary intestinal T-cell and natural killer-cell lymphomas: Clinicopathologic and prognostic features of 79 cases in South China.

Na Guo, Chunlu Zhou, Yu Wang, Jia Fu, Yueqiong Chen, Fang Wang, Huilan Rao

Abstract read
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Article in American journal of clinical pathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Na GuoZhejiang Cancer Hospital Ringgold, Hangzhou, Zhejiang, China.
Chunlu ZhouDepartment of Pathology, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China.
Yu WangDepartment of Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China.
Jia FuDepartment of Pathology, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China.
Yueqiong ChenDepartment of Pathology, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China.
Fang WangDepartment of Molecular Diagnostics, Sun Yat-sen University Cancer Center Ringgold, Guangzhou, Guangdong, China.
Huilan RaoDepartment of Pathology, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China.

Funding

Medical Science and Technology Program of Guangdong Province A 2018001Natural Science Foundation of Guangdong Province 2018A030313663
6 · The paper itself

Abstract

objectivesPrimary intestinal T-cell and natural killer-cell lymphomas (PITNKLs) are aggressive and make pathologic diagnoses in biopsy specimens challenging. We analyzed different subtypes' clinicopathologic features and treatment outcomes.

methodsSeventy-nine PITNKL cases were characterized by clinical, morphologic, and immunohistochemical features.

resultsAmong 79 cases of PITNKLs from 2008 to 2017 in our institution, 40 (50.63%) were extranodal NK/T-cell lymphoma, nasal type (ENKTL); 32 (40.51%) monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL); 6 (7.59%) intestinal T-cell lymphoma, not otherwise specified; and 1 (1.27%) indolent T-cell lymphoma of the gastrointestinal tract. Small intestine (n = 47) was the most common site. Monomorphic epitheliotropic intestinal T-cell lymphoma showed distinctive clinicopathologic features from other subtypes with high expression (96.88%) of spleen tyrosine kinase (SYK) and PD-L1 (87.5%) and the poorest prognosis (P < .001). CD30 was highly expressed in ENKTL (9/17, 57.94%) and irrelevant to prognosis (P > .05).

conclusionsCases of PITNKL are biologically heterogeneous; most have a dismal prognosis. SYK and PD-L1 expression might be a significant marker for MEITL and helps differential diagnosis.

Indexed as

Intestinal NeoplasmsKiller Cells, NaturalLymphoma, Extranodal NK-T-CellLymphoma, T-CellAdolescentAdultAgedAged, 80 and overBiomarkers, TumorChildChinaFemaleHumansMaleMiddle AgedPrognosisBiomarkers, TumorMEITLPD-L1primary intestinal T-cell and NK-cell lymphomasSYK

Identifiers

PMID39121027
PMCPMC11775117

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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.