Frequent occurrence of BCL6 rearrangements in nodular lymphocyte predominance Hodgkin lymphoma but not in classical Hodgkin lymphoma

Author:

Wlodarska Iwona1,Nooyen Peet1,Maes Brigitte1,Martı́n-Subero José I.1,Siebert Reiner1,Pauwels Patrick1,De Wolf-Peeters Chris1,Hagemeijer Anne1

Affiliation:

1. From the Center for Human Genetics, Catholic University of Leuven, Leuven, Belgium; the Department of Pathology, Stichting PAMM, Eindhoven, the Netherlands; the Division for Morphology and Molecular Pathology, Catholic University of Leuven, Leuven, Belgium; and the Institute of Human Genetics, University Hospital, Kiel, Germany.

Abstract

We studied the genomic status of BCL6 in 23 cases of nodular lymphocyte predominance Hodgkin lymphoma (NLPHL) and 40 cases of classical Hodgkin lymphoma (cHL), using dual-color interphase fluorescence in situ hybridization (FISH). The BCL6rearrangement was identified in 48% of NLPHL cases and was not detected in cHL cases. As a confirmation, sequential or simultaneous immunohistochemistry (IHC) and FISH using CD20 or BCL6 antibodies and BCL6 DNA probes was performed in 8 NLPHL cases. The BCL6-associated translocations, t(3;22)(q27;q11), t(3;7)(q27;p12), and the most probable t(3;9)(q27;p13), were identified in 3 cases. A consistent expression of BCL6 protein in popcorn cells with the highest number of intensely stained cells in cases with a genomic BCL6rearrangement was shown by IHC. These findings support the hypothesis of a germinal center B cell–derived origin of NLPHL, indicate a significant role of BCL6 in the pathogenesis of NLPHL, and provide further evidence of the genetic diversity underlying the pathogenesis of NLPHL and cHL.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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