Evidence map›Paper›PMID 39379519›Full record

ArticleVirchows Archiv : an international journal of pathology2024

Pediatric-type follicular lymphoma and pediatric nodal marginal zone lymphoma: additional evidence to support they are a single disease with variation in the histologic spectrum.

Huan-Ge Li, Xiang-Nan Jiang, Tian Xue, Bei-Bei Xin, Lian Chen, Gui-Xin Li, Qian Wang, Qin-Qin Hou, Xu Cai, Xiao-Yan Zhou and 1 more

Abstract read
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

11 authors.

Huan-Ge Li *Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Xiang-Nan Jiang *Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Tian XueDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Bei-Bei XinShanghai Rightongene Biotechnology Co., Ltd., Shanghai, 201403, China.
Lian ChenDepartment of Pathology, Children's Hospital of Fudan University, Shanghai, 201102, China.
Gui-Xin LiDepartment of Gastroenterology, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200233, China.
Qian WangDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Qin-Qin HouDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Xu CaiDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Xiao-Yan ZhouDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Xiao-Qiu LiDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. leexiaoqiu@hotmail.com.ORCID http://orcid.org/0000-0002-1774-3092

Funding

Chinese Society of Clinical Oncology Y-NCJH202202-0028Chinese Society of Clinical Oncology Y-XD202001-0152Science and Technology Commission of Shanghai Municipality 22YF1408200Shanghai Anticancer Association SOAR PROJECT SACA- AX202204Shanghai Municipal Health Commission 202040074
6 · The paper itself

Abstract

Pediatric-type follicular lymphoma (PTFL) and pediatric nodal marginal zone lymphoma (PNMZL) are two rare indolent B-cell lymphomas with overlapping features. Recently, cases showing hybridizing features of PTFL and PNMZL have been reported. Herein, we retrospectively analyzed the clinicopathologic features of 59 patients, including 39 with PTFL, 5 with PNMZL, and 15 with mixed-type tumors (MTT). And next-generation sequencing analysis was performed on 3 PTFL, 2 PNMZL, and 2 MTT cases. In addition, previously published mutational data of 96 PTFLs, 25 PNMZLs, and 46 MTTs were also analyzed. There were 52 male and 7 female patients, with a median age of 17 years. Most patients (96.6%) had lymph node involvement in the head and neck region and were diagnosed with stage I disease. Among the 50 patients (85%) with telephone follow-up, 44 (88%) adopted a watch-and-wait strategy after surgical resection of the lesions. Only one PTFL patient experienced a relapse 6 months after diagnosis. Microscopically, not only the MTT cases showed a composite form of enlarged follicles and interfollicular lymphocytic proliferation producing a progressively transformed germinal center (PTGC) pattern, but also focal follicles with a PTGC-like pattern were observed in PTFL cases. Genetically, the most frequently mutated genes were TNFRSF14 (in 3 PTFLs and 2 MTTs), MAP2K1 (in 2 PTFLs, 1 PNMZL and 1 MTT), and IRF8 (in 2 MTTs and 1 PNMZL). Based on the similar or overlapping clinical, pathologic, and genetic features, PTFL and PNMZL are likely to represent two different histologic patterns of the same disease.

Indexed as

Lymphoma, B-Cell, Marginal ZoneLymphoma, FollicularAdolescentAdultBiomarkers, TumorChildChild, PreschoolFemaleHigh-Throughput Nucleotide SequencingHumansLymph NodesMaleMutationRetrospective StudiesYoung AdultBiomarkers, TumorGene mutationNext-generation sequencingPediatric nodal marginal zone lymphomaPediatric-type follicular lymphoma

Identifiers

PMID39379519
PMCPMC11564197

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

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 Socratic graph.