Evidence map›Paper›PMID 41076559›Full record

ArticleHematological oncology2025

Tissue-Equivalents of Lymphoid Clonal Hematopoiesis of Indeterminate Potential (L-CHIP) and Germline-Derived Lymphoproliferations: Possible Caveats for Hematopathologists.

Magdalena M Brune, Ivana Bratic Hench, Stefan Dirnhofer, Alexandar Tzankov

Abstract read
In one paragraph

Article in Hematological oncology, 2025. 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

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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

1 citing paper in PubMed.

  1. Article
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

4 authors.

Magdalena M BruneInstitute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.ORCID https://orcid.org/0000-0002-9236-1377
Ivana Bratic HenchInstitute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.
Stefan DirnhoferInstitute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.
Alexandar TzankovInstitute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.ORCID https://orcid.org/0000-0002-1100-3819

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clonal hematopoiesis of indeterminate potential (CHIP) is a predisposing condition to lymphoma development. CHIP carrying mutations that are recurrently found in lymphomas are designated as L-CHIP. We presume that bone marrow-derived L-CHIP populations are able to expand and manifest in peripheral lymphoid tissues, where they could hence be called L-CHIP tissue-equivalents. There, they may proliferate and foster unexplained follicular hyperplasias, and, thus, potentially represent an early precursor of lymphoma. Analogously, we hypothesize that certain germline-derived mutations lead to lymphoproliferations (germline-derived lymphoproliferations) in otherwise healthy individuals. We collected seven exceptional cases of symptomatic nodal and extranodal lymphoid hyperplasias, which were all morphologically suspicious and displayed somatic and/or germline-derived mutations recurrently found in B-cell lymphomas. One patient developed follicular lymphoma after 8 years carrying the same non-productive immunoglobulin rearrangement detected in the initial biopsy. L-CHIP tissue-equivalents and germline-derived lymphoproliferations potentially represent first steps in lymphomagenesis and knowledge about their existence might be of diagnostic utility in challenging cases of (atypical) lymphoproliferations. With histology, immunohistochemistry, and molecular testing, such lesions can be identified in situ.

Indexed as

Clonal HematopoiesisGerm-Line MutationLymphoproliferative DisordersAdultAgedFemaleHumansMaleMiddle Agedclonal hematopoiesisgermline‐derived variantlymphomagenesislymphoproliferationnext generation sequencing

Identifiers

PMID41076559
PMCPMC12515349

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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.