Aberrant Expression of Multiple T‐Cell Markers in Primary Cutaneous Follicle Center Lymphoma: A Rare Case Report

Aberrant expression of T-cell markers in B-cell lymphomas is rare and can pose diagnostic challenges. We report a case of a 65-year-old man presenting with newly developed scalp nodules. Histopathology revealed nodular lymphoid infiltrates composed of large centrocytes and centroblasts. Immunohistochemistry demonstrated CD20, BCL6, CD10, and MEF2B positivity with monotypic kappa light chain expression, confirming B-cell lineage. Notably, aberrant co-expression of multiple T-cell markers (CD2, CD3, CD4, and partial CD5), with weaker intensity than surrounding T-cells, was observed. Molecular studies showed clonal immunoglobulin heavy chain rearrangement with a polyclonal T-cell receptor pattern. These findings established the diagnosis of primary cutaneous follicle center lymphoma (PCFCL) with aberrant T-cell marker expression. This represents the first reported case of PCFCL with aberrant expression of multiple T-cell markers, emphasizing the importance of comprehensive immunophenotyping for accurate lymphoma classification.

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Publication Details

Journal
Journal of Cutaneous Pathology
Published
2026-09-06
DOI
https://doi.org/10.1111/cup.70207
Primary Topic
Cutaneous lymphoproliferative disorders research
Type
article
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article

Aberrant Expression of Multiple T‐Cell Markers in Primary Cutaneous Follicle Center Lymphoma: A Rare Case Report

Vanessa Pfefferle, Stephan Forchhammer, Antonio Vogelsberg, Christian M. Schürch et al.
Journal of Cutaneous Pathology
Cutaneous lymphoproliferative disorders research
article

Aberrant Expression of Multiple T‐Cell Markers in Primary Cutaneous Follicle Center Lymphoma: A Rare Case Report

Vanessa Pfefferle, Stephan Forchhammer, Antonio Vogelsberg, Christian M. Schürch, M. Maaß
article en

Abstract

Aberrant expression of T-cell markers in B-cell lymphomas is rare and can pose diagnostic challenges. We report a case of a 65-year-old man presenting with newly developed scalp nodules. Histopathology revealed nodular lymphoid infiltrates composed of large centrocytes and centroblasts. Immunohistochemistry demonstrated CD20, BCL6, CD10, and MEF2B positivity with monotypic kappa light chain expression, confirming B-cell lineage. Notably, aberrant co-expression of multiple T-cell markers (CD2, CD3, CD4, and partial CD5), with weaker intensity than surrounding T-cells, was observed. Molecular studies showed clonal immunoglobulin heavy chain rearrangement with a polyclonal T-cell receptor pattern. These findings established the diagnosis of primary cutaneous follicle center lymphoma (PCFCL) with aberrant T-cell marker expression. This represents the first reported case of PCFCL with aberrant expression of multiple T-cell markers, emphasizing the importance of comprehensive immunophenotyping for accurate lymphoma classification.

Journal of Cutaneous Pathology
Research Institute for Work, Technology and Culture (DE), University Children's Hospital Tübingen (DE), Bernstein Center for Computational Neuroscience Tübingen (DE), University of Tübingen (DE)
Openalex Percentile: Top 9%
Cutaneous lymphoproliferative disorders research
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Aberrant Expression of Multiple T‐Cell Markers in Primary Cutaneous Follicle Center Lymphoma: A Rare Case Report — Vanessa Pfefferle, Stephan Forchhammer, et al. · Journal of Cutaneous Pathology (2026) | TGRS Research Map | TGRS