Splenic red pulp lymphoma with numerous basophilic villous lymphocytes: a distinct clinicopathologic and molecular entity?

Author:

Traverse-Glehen Alexandra12,Baseggio Lucile23,Bauchu Evelyne Callet-23,Morel Dominique23,Gazzo Sophie23,Ffrench Martine23,Verney Aurélie2,Rolland Delphine2,Thieblemont Catherine24,Magaud Jean-Pierre23,Salles Gilles24,Coiffier Bertrand24,Berger Françoise12,Felman Pascale23

Affiliation:

1. Service d'Anatomie Pathologique Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, Lyon, France;

2. Unité Mixte de Recherche commune au Centre National de Recherche Scientifique (UMR CNRS) 5239 Equipe “Pathologie des Cellules Lymphoides,” Université Lyon 1, Lyon, France;

3. Laboratoire d'Hématologie Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, Lyon, France; and

4. Service d'Hématologie Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, Lyon, France

Abstract

The presence of circulating villous lymphocytes (VLs) in lymphoma patients usually points to splenic marginal zone B-cell lymphoma (SMZL), even if the VLs can be found occasionally in other small B-cell lymphomas. However, those cells are variably described, and detailed cytologic characterization is often lacking. We identified lymphoma cases with numerous basophilic VLs among the large group of splenic lymphoma with VLs, and for further delineation, 37 cases with this particular cytology were analyzed. Patients, predominantly older men, presented with moderate lymphocytosis and splenomegaly without pancytopenia. The monoclonal B cells expressed IgM + D, IgM + G, IgM or IgG, as well as CD76 and CD11c, frequently CD103, and rarely CD123. Spleen sections were peculiar, with atrophic white pulp and a monomorphic diffuse lymphoma infiltration in a congested red pulp. Bone marrow infiltration was interstitial and intrasinusoidal without extensive fibrosis. Cytogenetic analysis showed a frequent absence of clonal aberrations (68%). Most cases (79%) were IgH mutated, with an overrepresentation of VH3 and VH4 gene families. These results, as well as the clinical evolution, show that those lymphoma cases represent a homogeneous group distinct from SMZL and reminiscent of hairy cell leukemia variant, perhaps corresponding to a separate lymphoma entity.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference39 articles.

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