Peripheral T-cell lymphomas expressing CD30 and CD15 expand the spectrum of anaplastic large cell lymphoma, ALK-negative.

ALK‐negative CD15 CD30 anaplastic large cell lymphoma peripheral T‐cell lymphoma

Journal

British journal of haematology
ISSN: 1365-2141
Titre abrégé: Br J Haematol
Pays: England
ID NLM: 0372544

Informations de publication

Date de publication:
12 Apr 2024
Historique:
revised: 19 03 2024
received: 12 10 2023
accepted: 20 03 2024
medline: 13 4 2024
pubmed: 13 4 2024
entrez: 13 4 2024
Statut: aheadofprint

Résumé

Peripheral T-cell lymphomas (PTCL) are morphologically and biologically heterogeneous and a subset expresses CD30, including anaplastic large cell lymphomas (ALCL) and a minority of PTCL, not otherwise specified (PTCL, NOS). ALCL with ALK translocations (ALCL, ALK+) are readily identified by routine diagnostic methods, but differentiating ALCL without ALK translocation (ALCL, ALK-) and PTCL, NOS expressing CD30 (PTCL CD30+) can be challenging. Furthermore, rare PTCL co-express CD30 and CD15 (PTCL CD30+CD15+); some resemble ALCL, ALK- while others resemble classic Hodgkin lymphoma. To explore the relationship between PTCL CD30+CD15+ and ALCL, ALK-, we analysed 19 cases of PTCL with CD30 expression, previously diagnosed as ALCL, ALK- (nine cases) and PTCL CD30+CD15+ (10 cases) for DUSP22/IRF4 rearrangements, coding RNA expression and selected transcriptome analysis using the NanoString nCounter gene expression analysis platform. Unsupervised clustering showed no clear segregation between ALCL, ALK- and PTCL CD30+CD15+. Three cases previously classified as PTCL CD30+CD15+ showed DUSP22/IRF4 rearrangements, favouring a diagnosis of ALCL, ALK-. Our results suggest that cases previously designated PTCL CD30+CD15+, likely fall within the spectrum of ALCL, ALK-; additionally, a subset of ALCL, ALK- with DUSP22/IRF4 rearrangement expresses CD15, consistent with previous reports and expands the immunophenotypic spectrum of this lymphoma subgroup.

Identifiants

pubmed: 38613165
doi: 10.1111/bjh.19442
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.

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Auteurs

Karthik A Ganapathi (KA)

Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
Department of Laboratory Medicine, University of California, San Francisco, San Francisco, California, USA.

Alina Nicolae (A)

Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.

Caoimhe Egan (C)

Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.

Huimin Geng (H)

Department of Laboratory Medicine, University of California, San Francisco, San Francisco, California, USA.

Liqiang Xi (L)

Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.

Svetlana D Pack (SD)

Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.

Jason R McFadden (JR)

Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.

Mark Raffeld (M)

Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.

Elaine S Jaffe (ES)

Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.

Stefania Pittaluga (S)

Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.

Classifications MeSH