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Hepatic tuberculosis in human immunodeficiency virus co-infected adults: a case series of South African adults

BACKGROUND: Although Mycobacterium tuberculosis (TB) infection may cause extrapulmonary disease in HIV-infected adults, HIV-associated hepatic TB has been poorly characterized. Our objective was to describe hepatic TB in HIV-infected adults. METHODS: Retrospective study of patients diagnosed with he...

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Autores principales: Gounder, Lilishia, Moodley, Pravikrishnen, Drain, Paul K., Hickey, Andrew J., Moosa, Mahomed-Yunus S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288843/
https://www.ncbi.nlm.nih.gov/pubmed/28148232
http://dx.doi.org/10.1186/s12879-017-2222-2
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author Gounder, Lilishia
Moodley, Pravikrishnen
Drain, Paul K.
Hickey, Andrew J.
Moosa, Mahomed-Yunus S.
author_facet Gounder, Lilishia
Moodley, Pravikrishnen
Drain, Paul K.
Hickey, Andrew J.
Moosa, Mahomed-Yunus S.
author_sort Gounder, Lilishia
collection PubMed
description BACKGROUND: Although Mycobacterium tuberculosis (TB) infection may cause extrapulmonary disease in HIV-infected adults, HIV-associated hepatic TB has been poorly characterized. Our objective was to describe hepatic TB in HIV-infected adults. METHODS: Retrospective study of patients diagnosed with hepatic TB from 2005–2012 at Infectious Diseases Clinic, King Edward VIII Hospital, Durban, South Africa. RESULTS: Among twenty cases of histology-confirmed HIV-associated hepatic TB, median CD4 count was 47 cells/μl (inter-quartile range 27–107 cells/μl) and 75% (15/20) of patients had pre-existing pulmonary TB. The most frequent clinical finding was hepatomegaly (85%). Liver enzyme abnormalities included elevated alkaline phosphatase (median 456 u/L, inter-quartile range 322–1,043 u/L) and gamma-glutamyltransferase (median 422 u/L, inter-quartile range 235–736 u/L). Acid-fast bacilli were cultured from liver tissue in 30% (6/20) of patients; 25% (5/20) identified as TB. With standard anti-TB therapy, liver enzymes improved within six months in 92% (11/12) of patients. One year after diagnosis, twelve patients resolved clinically, two patients developed drug-resistant TB and six patients died. CONCLUSION: In our case series of HIV-infected patients, hepatic TB occurred in patients with severe immunosuppression, who presented with hepatomegaly and abnormal liver enzymes. More than half of patients had resolution of liver function by six months however the 12-month mortality remained high.
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spelling pubmed-52888432017-02-06 Hepatic tuberculosis in human immunodeficiency virus co-infected adults: a case series of South African adults Gounder, Lilishia Moodley, Pravikrishnen Drain, Paul K. Hickey, Andrew J. Moosa, Mahomed-Yunus S. BMC Infect Dis Research Article BACKGROUND: Although Mycobacterium tuberculosis (TB) infection may cause extrapulmonary disease in HIV-infected adults, HIV-associated hepatic TB has been poorly characterized. Our objective was to describe hepatic TB in HIV-infected adults. METHODS: Retrospective study of patients diagnosed with hepatic TB from 2005–2012 at Infectious Diseases Clinic, King Edward VIII Hospital, Durban, South Africa. RESULTS: Among twenty cases of histology-confirmed HIV-associated hepatic TB, median CD4 count was 47 cells/μl (inter-quartile range 27–107 cells/μl) and 75% (15/20) of patients had pre-existing pulmonary TB. The most frequent clinical finding was hepatomegaly (85%). Liver enzyme abnormalities included elevated alkaline phosphatase (median 456 u/L, inter-quartile range 322–1,043 u/L) and gamma-glutamyltransferase (median 422 u/L, inter-quartile range 235–736 u/L). Acid-fast bacilli were cultured from liver tissue in 30% (6/20) of patients; 25% (5/20) identified as TB. With standard anti-TB therapy, liver enzymes improved within six months in 92% (11/12) of patients. One year after diagnosis, twelve patients resolved clinically, two patients developed drug-resistant TB and six patients died. CONCLUSION: In our case series of HIV-infected patients, hepatic TB occurred in patients with severe immunosuppression, who presented with hepatomegaly and abnormal liver enzymes. More than half of patients had resolution of liver function by six months however the 12-month mortality remained high. BioMed Central 2017-02-01 /pmc/articles/PMC5288843/ /pubmed/28148232 http://dx.doi.org/10.1186/s12879-017-2222-2 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Gounder, Lilishia
Moodley, Pravikrishnen
Drain, Paul K.
Hickey, Andrew J.
Moosa, Mahomed-Yunus S.
Hepatic tuberculosis in human immunodeficiency virus co-infected adults: a case series of South African adults
title Hepatic tuberculosis in human immunodeficiency virus co-infected adults: a case series of South African adults
title_full Hepatic tuberculosis in human immunodeficiency virus co-infected adults: a case series of South African adults
title_fullStr Hepatic tuberculosis in human immunodeficiency virus co-infected adults: a case series of South African adults
title_full_unstemmed Hepatic tuberculosis in human immunodeficiency virus co-infected adults: a case series of South African adults
title_short Hepatic tuberculosis in human immunodeficiency virus co-infected adults: a case series of South African adults
title_sort hepatic tuberculosis in human immunodeficiency virus co-infected adults: a case series of south african adults
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288843/
https://www.ncbi.nlm.nih.gov/pubmed/28148232
http://dx.doi.org/10.1186/s12879-017-2222-2
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