Malignant lymphomas (ML) and HIV infection in Tanzania

<p>Abstract</p> <p>Background</p> <p>HIV infection is reported to be associated with some malignant lymphomas (ML) so called AIDS-related lymphomas (ARL), with an aggressive behavior and poor prognosis. The ML frequency, pathogenicity, clinical patterns and possible ass...

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Main Authors: Mwakigonja Amos R, Kaaya Ephata E, Mgaya Edward M
Format: Article
Language:English
Published: BMC 2008-06-01
Series:Journal of Experimental & Clinical Cancer Research
Online Access:http://www.jeccr.com/content/27/1/9
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spelling doaj-ad0e0b07e7284186a7e95065f79437452020-11-25T01:00:28ZengBMCJournal of Experimental & Clinical Cancer Research1756-99662008-06-01271910.1186/1756-9966-27-9Malignant lymphomas (ML) and HIV infection in TanzaniaMwakigonja Amos RKaaya Ephata EMgaya Edward M<p>Abstract</p> <p>Background</p> <p>HIV infection is reported to be associated with some malignant lymphomas (ML) so called AIDS-related lymphomas (ARL), with an aggressive behavior and poor prognosis. The ML frequency, pathogenicity, clinical patterns and possible association with AIDS in Tanzania, are not well documented impeding the development of preventive and therapeutic strategies.</p> <p>Methods</p> <p>Sections of 176 archival formalin-fixed paraffin-embedded biopsies of ML patients at Muhimbili National Hospital (MNH)/Muhimbili University of Health and Allied Sciences (MUHAS), Tanzania from 1996–2001 were stained for hematoxylin and eosin and selected (70) cases for expression of pan-leucocytic (CD45), B-cell (CD20), T-cell (CD3), Hodgkin/RS cell (CD30), histiocyte (CD68) and proliferation (Ki-67) antigen markers. Corresponding clinical records were also evaluated. Available sera from 38 ML patients were screened (ELISA) for HIV antibodies.</p> <p>Results</p> <p>The proportion of ML out of all diagnosed tumors at MNH during the 6 year period was 4.2% (176/4200) comprising 77.84% non-Hodgkin (NHL) including 19.32% Burkitt's (BL) and 22.16% Hodgkin's disease (HD). The ML tumors frequency increased from 0.42% (1997) to 0.70% (2001) and 23.7% of tested sera from these patients were HIV positive. The mean age for all ML was 30, age-range 3–91 and peak age was 1–20 years. The male:female ratio was 1.8:1. Supra-diaphragmatic presentation was commonest and histological sub-types were mostly aggressive B-cell lymphomas however, no clear cases of primary effusion lymphoma (PEL) and primary central nervous system lymphoma (PCNSL) were diagnosed.</p> <p>Conclusion</p> <p>Malignant lymphomas apparently, increased significantly among diagnosed tumors at MNH between 1996 and 2001, predominantly among the young, HIV infected and AIDS patients. The frequent aggressive clinical and histological presentation as well as the dominant B-immunophenotype and the HIV serology indicate a pathogenic association with AIDS. Therefore, routine HIV screening of all malignant lymphoma patients at MNH is necessary to enable comprehensive ARL diagnosis and formulation of preventive and therapeutic protocols.</p> http://www.jeccr.com/content/27/1/9
collection DOAJ
language English
format Article
sources DOAJ
author Mwakigonja Amos R
Kaaya Ephata E
Mgaya Edward M
spellingShingle Mwakigonja Amos R
Kaaya Ephata E
Mgaya Edward M
Malignant lymphomas (ML) and HIV infection in Tanzania
Journal of Experimental & Clinical Cancer Research
author_facet Mwakigonja Amos R
Kaaya Ephata E
Mgaya Edward M
author_sort Mwakigonja Amos R
title Malignant lymphomas (ML) and HIV infection in Tanzania
title_short Malignant lymphomas (ML) and HIV infection in Tanzania
title_full Malignant lymphomas (ML) and HIV infection in Tanzania
title_fullStr Malignant lymphomas (ML) and HIV infection in Tanzania
title_full_unstemmed Malignant lymphomas (ML) and HIV infection in Tanzania
title_sort malignant lymphomas (ml) and hiv infection in tanzania
publisher BMC
series Journal of Experimental & Clinical Cancer Research
issn 1756-9966
publishDate 2008-06-01
description <p>Abstract</p> <p>Background</p> <p>HIV infection is reported to be associated with some malignant lymphomas (ML) so called AIDS-related lymphomas (ARL), with an aggressive behavior and poor prognosis. The ML frequency, pathogenicity, clinical patterns and possible association with AIDS in Tanzania, are not well documented impeding the development of preventive and therapeutic strategies.</p> <p>Methods</p> <p>Sections of 176 archival formalin-fixed paraffin-embedded biopsies of ML patients at Muhimbili National Hospital (MNH)/Muhimbili University of Health and Allied Sciences (MUHAS), Tanzania from 1996–2001 were stained for hematoxylin and eosin and selected (70) cases for expression of pan-leucocytic (CD45), B-cell (CD20), T-cell (CD3), Hodgkin/RS cell (CD30), histiocyte (CD68) and proliferation (Ki-67) antigen markers. Corresponding clinical records were also evaluated. Available sera from 38 ML patients were screened (ELISA) for HIV antibodies.</p> <p>Results</p> <p>The proportion of ML out of all diagnosed tumors at MNH during the 6 year period was 4.2% (176/4200) comprising 77.84% non-Hodgkin (NHL) including 19.32% Burkitt's (BL) and 22.16% Hodgkin's disease (HD). The ML tumors frequency increased from 0.42% (1997) to 0.70% (2001) and 23.7% of tested sera from these patients were HIV positive. The mean age for all ML was 30, age-range 3–91 and peak age was 1–20 years. The male:female ratio was 1.8:1. Supra-diaphragmatic presentation was commonest and histological sub-types were mostly aggressive B-cell lymphomas however, no clear cases of primary effusion lymphoma (PEL) and primary central nervous system lymphoma (PCNSL) were diagnosed.</p> <p>Conclusion</p> <p>Malignant lymphomas apparently, increased significantly among diagnosed tumors at MNH between 1996 and 2001, predominantly among the young, HIV infected and AIDS patients. The frequent aggressive clinical and histological presentation as well as the dominant B-immunophenotype and the HIV serology indicate a pathogenic association with AIDS. Therefore, routine HIV screening of all malignant lymphoma patients at MNH is necessary to enable comprehensive ARL diagnosis and formulation of preventive and therapeutic protocols.</p>
url http://www.jeccr.com/content/27/1/9
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