Abstract

Abstract Follicular lymphoma (FL) is a morphologically and genetically well-characterized B-cell non-Hodgkin lymphoma that can show predominantly follicular, combined follicular and diffuse, or predominantly diffuse growth patterns. Although approximately 85% of FLs harbor the translocation t(14;18)(q32;q21) and consistently display a follicular growth pattern, predominantly diffuse FLs are less well characterized on the phenotypical, molecular, and clinical level. We studied 35 predominantly diffuse FL by immunohistochemistry, classical chromosome banding analysis, fluorescence in situ hybridization (FISH), and gene expression profiling. A total of 28 of 29 analyzable cases lacked t(14;18), and 27 of 29 cases revealed a unifying chromosomal aberration, a deletion in 1p36. Morphologically, 12 FLs were grade 1 and 23 were grade 2, and the immunophenotype with frequent expression of CD10, BCL6, and CD23 was in line with a germinal center B-cell phenotype. The gene expression profiles of 4 predominantly diffuse FLs fell into the spectrum of typical FL, with a unique enrichment of specific gene signatures. Remarkably, patients with diffuse FL frequently presented with low clinical stage and large but localized inguinal tumors. These results suggest that predominantly diffuse FL represent a distinct subtype of t(14;18)-negative nodal FL with a unifying genetic alteration (deletion of 1p36) and characteristic clinical features.

Keywords

BCL6BiologyFluorescence in situ hybridizationFollicular lymphomaImmunophenotypingGerminal centerComparative genomic hybridizationDiffuse large B-cell lymphomaLymphomaPathologyPhenotypeChromosomal translocationCytogeneticsMolecular biologyChromosomeGeneGeneticsB cellFlow cytometryImmunologyMedicineAntibody

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Year
2008
Type
article
Volume
113
Issue
5
Pages
1053-1061
Citations
144
Access
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Tiemo Katzenberger, Jörg Kalla, Ellen Leich et al. (2008). A distinctive subtype of t(14;18)-negative nodal follicular non-Hodgkin lymphoma characterized by a predominantly diffuse growth pattern and deletions in the chromosomal region 1p36. Blood , 113 (5) , 1053-1061. https://doi.org/10.1182/blood-2008-07-168682

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DOI
10.1182/blood-2008-07-168682