Gray-zone Lymphoma Between cHL and Large B-Cell Lymphoma: A Histopathologic Series From the LYSA.


Journal

The American journal of surgical pathology
ISSN: 1532-0979
Titre abrégé: Am J Surg Pathol
Pays: United States
ID NLM: 7707904

Informations de publication

Date de publication:
03 2019
Historique:
pubmed: 13 12 2018
medline: 10 1 2020
entrez: 13 12 2018
Statut: ppublish

Résumé

Gray-zone lymphoma (GZL) with features intermediate between classic Hodgkin lymphoma (cHL) and large B-cell lymphoma (LBCL) was introduced as a provisional entity into the World Health Organization classification in 2008. However, as diagnostic criteria are imprecise, reliable identification of GZL cases remains challenging. Here, we describe the histopathologic features of 139 GZL cases from a retrospective Lymphoma Study Association (LYSA) study with the goal to improve classification accuracy. Inclusion criteria were based on literature review and an expert consensus opinion of the LYSA hematopathologist panel. We observed 86 cases with a morphology more closely related to cHL, but with an LBCL immunophenotype based on strong and homogenous B-cell marker expression (CD20 and/or CD79a, OCT2, BOB1, PAX5) on all tumor cells (cHL-like GZL). Fifty-three cases were morphologically more closely related to LBCL but harbored a cHL immunophenotype (LBCL-like GZL). Importantly, we observed a continuous morphologic and immunophenotypic spectrum within these 2 GZL categories. The majority of cases presented genetic immune escape features with CD274/PDCD1LG2 and/or CIITA structural variants by fluorescence in situ hybridization. Patients without mediastinal involvement at diagnosis (17%) were older than those with mediastinal tumors (median: 56 vs. 39 y). Cases associated with Epstein-Barr virus (24%) presented with similar patient characteristics and outcome as Epstein-Barr virus negative cases. In summary, we provide refined diagnostic criteria that contribute to a more precise pathologic and clinical characterization of GZL within a broad spectrum from cHL-like to LBCL-like disease.

Identifiants

pubmed: 30540571
doi: 10.1097/PAS.0000000000001198
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

341-351

Auteurs

Clémentine Sarkozy (C)

Hospital, Hematology Department, Hospices Civils Lyon, Lyon-Sud.
INSERM1052, CNRS 5286, Lyon-Sud Charles Mérieux Lyon-1 Faculty, Claude Bernard University.
Department for Lymphoid Cancer Research, Centre for Lymphoid Cancer, BC Cancer, Vancouver, BC, Canada.

Christiane Copie-Bergman (C)

Pathology Department, Henri Mondor-Albert Chennevier Hospital, APHP, Paris Est-Créteil (UPEC) University Faculty, UMR-S 955, INSERM, Créteil.

Diane Damotte (D)

Pathology Department, Groupe Hospitalier Cochin, APHP, Paris Descartes University-Sorbonne Paris Cité.

Susana Ben-Neriah (S)

Department for Lymphoid Cancer Research, Centre for Lymphoid Cancer, BC Cancer, Vancouver, BC, Canada.

Barbara Burroni (B)

Pathology Department, Groupe Hospitalier Cochin, APHP, Paris Descartes University-Sorbonne Paris Cité.

Jérome Cornillon (J)

Hematology Department, Lucien Neuwirth Cancer Institut, St Priest en Jarez.

Richard Lemal (R)

Hematology Department, CHU Clermont-Ferrand.

Camille Golfier (C)

Hematology Department, CHU Dijon.

Bettina Fabiani (B)

Pathology Department, Hôpital Saint Antoine, APHP.

Catherine Chassagne-Clément (C)

Pathology Department, Centre Léon Bérard, Lyon.

Marie Parrens (M)

Pathology Department, CHU de Bordeaux.

Charles Herbaux (C)

Hematology Department, CHRU de Lille.

Luc Xerri (L)

Cancer Research Center of Marseille, Inserm U1068/CNRS U7258, Institut Paoli-Calmettes, Aix Marseille Université, Marseille.

Celine Bossard (C)

Pathology Department, CHU de Nantes.

Camille Laurent (C)

Pathology Department, Institut Universitaire du Cancer-Oncopole, CHU Toulouse, INSERM, U.1037, Centre de recherche en cancérologie de Toukouse-Purpan, Toulouse.

Morgane Cheminant (M)

Clinical Hematology, Necker-Enfants Malades University Hospital, AP-HP, Paris Descartes University-Sorbonne Paris Cité, Paris.

Guillaume Cartron (G)

Hematology Department, CHU Montpellier.

Jose Cabecadas (J)

Departamento de Diagnóstico Laboratorial, Instituto Português de Oncologia de Lisboa-IPO, Lisbon.

Thierry Molina (T)

Necker Enfants Malades Hospital, Université Paris Descartes, APHP.

Gilles Salles (G)

Hospital, Hematology Department, Hospices Civils Lyon, Lyon-Sud.
INSERM1052, CNRS 5286, Lyon-Sud Charles Mérieux Lyon-1 Faculty, Claude Bernard University.

Christian Steidl (C)

Department for Lymphoid Cancer Research, Centre for Lymphoid Cancer, BC Cancer, Vancouver, BC, Canada.

Hervé Ghesquières (H)

Hospital, Hematology Department, Hospices Civils Lyon, Lyon-Sud.
INSERM1052, CNRS 5286, Lyon-Sud Charles Mérieux Lyon-1 Faculty, Claude Bernard University.

Anja Mottok (A)

Department for Lymphoid Cancer Research, Centre for Lymphoid Cancer, BC Cancer, Vancouver, BC, Canada.
Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany.

Alexandra Traverse-Glehen (A)

INSERM1052, CNRS 5286, Lyon-Sud Charles Mérieux Lyon-1 Faculty, Claude Bernard University.
Pathology Department, Hospices Civils de Lyon, Centre Hospitalier Lyon-Sud69495 Pierre Bénite Cedex.

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