Evidence map›Paper›PMID 41814313›Full record

ArticleWorld journal of surgical oncology2026

Novel LUC7L::NUTM1 fusion in PDGFRA-rearranged myeloproliferative neoplasm with eosinophilia: a case report.

Jing Zhou, Hanbing Yao, Jiarong Ren, Ke Sun, Dongxue Chen, Rui Zhang, Gangfeng Wang

Abstract readCase Reports
In one paragraph

Article in World journal of surgical 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

What it found

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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

The trial behind it

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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

7 authors.

Jing ZhouDepartment of Hematology, Xi'an International Medical Center, No. 777 Xitai Road, Gaoxin District, Xi'an, 710100, China.
Hanbing YaoDepartment of Hematology, Xi'an International Medical Center, No. 777 Xitai Road, Gaoxin District, Xi'an, 710100, China.
Jiarong RenDepartment of Hematology, Xi'an International Medical Center, No. 777 Xitai Road, Gaoxin District, Xi'an, 710100, China.
Ke SunDepartment of Hematology, Xi'an International Medical Center, No. 777 Xitai Road, Gaoxin District, Xi'an, 710100, China.
Dongxue ChenDepartment of Hematology, Xi'an International Medical Center, No. 777 Xitai Road, Gaoxin District, Xi'an, 710100, China.
Rui ZhangDepartment of Hematology, Xi'an International Medical Center, No. 777 Xitai Road, Gaoxin District, Xi'an, 710100, China.
Gangfeng WangDepartment of Hematology, Xi'an International Medical Center, No. 777 Xitai Road, Gaoxin District, Xi'an, 710100, China. xibeiwgf@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myeloid/lymphoid neoplasm with PDGFRA rearrangement are a group of haematologic tumors, in which the clonal proliferation of precursor eosinophils leads to persistent eosinophilic hyperplasia, and varying degrees of involvement of the liver, spleen and lymph nodes. While PDGFRA rearrangements are frequently observed in mpn-eo, the co-occurrence of t(15;16)(q14;p13) translocations leading to LUC7L::NUTM1 fusion genes has not been previously documented. Here we present a 30-year-old male patient with leukocytosis and generalized lymphadenopathy. Bone marrow cytology revealed eosinophilia with abnormal and atypical granulocytes showing dysplastic cytoplasmic granules. Cytogenetic analysis identified t(15;16)(q14;p13), while RNA sequencing confirmed the novel LUC7L::NUTM1 fusion gene and co-detected FIP1L1::PDGFRA fusion gene. The patient achieved stable disease imatinib (100 mg/day) treatment. This first report of dual PDGFRA/NUTM1 fusions expands the molecular spectrum of MPN-Eo and highlights the therapeutic implications of novel fusion detection.

Indexed as

EosinophiliaGene RearrangementMyeloproliferative DisordersNuclear ProteinsOncogene Proteins, FusionReceptor, Platelet-Derived Growth Factor alphaAdultHumansImatinib MesylateMalemRNA Cleavage and Polyadenylation FactorsPrognosisTranslocation, GeneticFIP1L1-PDGFRA fusion protein, humanImatinib MesylatemRNA Cleavage and Polyadenylation FactorsNuclear ProteinsOncogene Proteins, FusionReceptor, Platelet-Derived Growth Factor alphaCase reportEosinophiliaLUC7L2LUC7L:NUTM1 fusionPDGFRA

Identifiers

PMID41814313
PMCPMC13122892

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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.