Acta Haematologica

Original Paper

Genetic and Immunohistochemical Characterization of Epstein-Barr Virus-Associated Diffuse Large B-Cell Lymphoma

Al-Humood S. · AlQallaf A. · Al-Shemmari S. · Al-Faris L. · Al-Ayadhy B.

Author affiliations

Department of Pathology, Faculty of Medicine, Kuwait University, Safat, Kuwait

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Acta Haematol 2014;131:1-10

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Article / Publication Details

First-Page Preview
Abstract of Original Paper

Received: July 25, 2012
Accepted: February 28, 2013
Published online: September 04, 2013
Issue release date: December 2013

Number of Print Pages: 10
Number of Figures: 5
Number of Tables: 5

ISSN: 0001-5792 (Print)
eISSN: 1421-9662 (Online)

For additional information: https://www.karger.com/AHA

Abstract

Epstein-Barr virus (EBV) has a pathogenic role in several lymphomas, including diffuse large B-cell lymphoma (DLBCL). EBV-associated genetic aberrations in DLBCL have not been fully characterized. The aim of this study was to investigate the prevalence of EBV infection in sporadic DLBCL cases in Kuwait and to evaluate their EBV status in relation to demographic data, the anatomical disease site, immunophenotypic features, particularly pertaining to the Choi's DLBCL prognostic classification, and chromosomal aberrations. Using immunohistochemistry (IHC), in situ hybridization (ISH), nested polymerase chain reaction (nPCR) and comparative genomic hybridization techniques, formalin-fixed paraffin-embedded blocks of archived DLBCL cases were included and evaluated in the study. EBV was detected in 6.9, 18.2 and 25% of the studied cases using IHC, ISH and nPCR, respectively, indicating that nPCR is more sensitive in detecting EBV than IHC and ISH. EBV- DLBCL cases showed BCL6 protein expression more frequently than EBV+ DLBCL cases. The reported prevalence of EBV+ DLBCL cases in this study is similar to that reported in the literature using ISH results and higher using nPCR results. There was a significant inverse correlation between BCL6 protein expression and the presence of EBV (p = 0.01).

© 2013 S. Karger AG, Basel




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Article / Publication Details

First-Page Preview
Abstract of Original Paper

Received: July 25, 2012
Accepted: February 28, 2013
Published online: September 04, 2013
Issue release date: December 2013

Number of Print Pages: 10
Number of Figures: 5
Number of Tables: 5

ISSN: 0001-5792 (Print)
eISSN: 1421-9662 (Online)

For additional information: https://www.karger.com/AHA


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