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Human immunodeficiency virus (HIV) and Epstein-Barr virus (EBV) related lymphomas, pathology view point.

Authors :
Linke-Serinsöz E
Fend F
Quintanilla-Martinez L
Source :
Seminars in diagnostic pathology [Semin Diagn Pathol] 2017 Jul; Vol. 34 (4), pp. 352-363. Date of Electronic Publication: 2017 Apr 07.
Publication Year :
2017

Abstract

The contribution of Epstein Barr virus (EBV) and Kaposi sarcoma herpes virus (KSHV) to the development of specific types of malignant lymphomas occurring in the human immunodeficiency virus (HIV) setting has been extensively studied since the beginning of the HIV epidemic 35 years ago. The introduction of highly active antiretroviral therapies (HAART) in 1996 has changed dramatically the incidence of HIV-related malignancies. Nevertheless, malignant lymphomas continue to be the major group of malignances observed in HIV infected individuals, and the most common cause of cancer related-deaths. Common features of the predominant B-cell lymphomas in the HIV <superscript>+</superscript> setting are the frequent plasmacytoid morphology of the neoplastic cells, advanced stage, aggressive disease and frequent extranodal involvement. In this article, we review the evolving concepts and definitions of the various EBV-associated lymphomas in HIV <superscript>+</superscript> patients, including diffuse large B-cell lymphoma, Burkitt lymphoma, classical Hodgkin lymphoma, plasmablastic lymphoma and primary effusion lymphoma. The current knowledge regarding the pathogenesis of these malignancies, the interplay between HIV and EBV co-infection in the development of certain HIV related lymphomas, and the emerging paradigm that suggests that HIV may play a direct role in lymphomagenesis are explored as well.<br /> (Copyright © 2017 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
0740-2570
Volume :
34
Issue :
4
Database :
MEDLINE
Journal :
Seminars in diagnostic pathology
Publication Type :
Academic Journal
Accession number :
28506687
Full Text :
https://doi.org/10.1053/j.semdp.2017.04.003