Evidence map›Paper›PMID 40511879›Full record

ArticleThe American journal of surgical pathology2025

IgM Immunohistochemical Expression is a Potential Risk Factor for Extracutaneous Dissemination in Patients With Primary Cutaneous Follicle Center Lymphoma.

Anne M R Schrader, Ruben A L de Groen, Rein Willemze, Patty M Jansen, Koen D Quint, Tom van Wezel, Ronald van Eijk, Dina Ruano, Cornelis P Tensen, Arjan Diepstra and 5 more

Abstract read
In one paragraph

Article in The American journal of surgical pathology, 2025. 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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0cells of the map it votes in
0citing papers in PubMed
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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

15 authors.

Anne M R SchraderDepartments of Pathology.
Ruben A L de GroenHematology, and.
Rein WillemzeDermatology, Leiden University Medical Center, Leiden.
Patty M JansenDepartments of Pathology.
Koen D QuintDermatology, Leiden University Medical Center, Leiden.
Tom van WezelDepartments of Pathology.
Ronald van EijkDepartments of Pathology.
Dina RuanoDepartments of Pathology.
Cornelis P TensenDermatology, Leiden University Medical Center, Leiden.
Arjan DiepstraDepartment of Pathology, University Medical Center Groningen, Groningen.
Anke van den BergDepartment of Pathology, University Medical Center Groningen, Groningen.
Lianne KoensDepartment of Pathology, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Naomi KakiailatuHematology, and.
Maarten H VermeerDermatology, Leiden University Medical Center, Leiden.
Joost S P VermaatHematology, and.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary cutaneous follicle center lymphoma (PCFCL) is a type of cutaneous B-cell lymphoma with an indolent behavior and a 5-year disease-specific survival of 95%. Given the difficulty of identifying patients at risk for developing extracutaneous dissemination (ECD), this study aimed to identify predictors in the clinical presentation, histopathology, immune phenotype, and genetic profile of PCFCL patients by comparing those who developed ECD with those whose disease remained skin limited (SL) during follow-up. After review of clinical data and histopathology, a total of 13 ECD-PCFCL patients and 15 SL-PCFCL patients with varying treatments were included from the Dutch Cutaneous Lymphomas Registry. At diagnosis, all patients presented with classic PCFCL lesions on the trunk or head-and-neck region, and histology indicated a predominance of centrocytes admixed with centroblasts. IgM expression was significantly more frequent in ECD-PCFCL (54%) than in SL-PCFCL (7%; P =0.006). Targeted next-generation sequencing (NGS) with a 200 B-cell lymphoma-related gene panel demonstrated known PCFCL-like mutations in both groups. In addition, ECD-PCFCL demonstrated an enrichment of mutations associated with the activated B-cell genotype, including MYD88 (n=2), and some unique mutations, such as in ERBB4 (n=4). In conclusion, this study identified IgM expression at diagnosis as a potential biomarker for extracutaneous spread in PCFCL. In IgM-positive cases, genetic testing may be warranted. Patients with uncommon mutational profiles, such as those resembling the ABC-DLBCL genotype, may particularly benefit from closer follow-up and consideration of more aggressive treatment, including immuno-polychemotherapy. As these observations were made in a limited number of patients, our results require validation in an independent cohort.

Indexed as

Biomarkers, TumorImmunoglobulin MImmunohistochemistryLymphoma, FollicularSkin NeoplasmsAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedMutationNetherlandsPhenotypePredictive Value of TestsBiomarkers, TumorImmunoglobulin Mextracutaneous disseminationgenetic profileIgMMYD88primary cutaneous follicle center lymphoma

Identifiers

PMID40511879
PMCPMC12352555

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.