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Diagnosis and treatment of microsporidial keratoconjunctivitis: literature review and case series

PURPOSE: The purpose of this study is to describe the clinical characteristics, microscopic findings, and treatment response to albendazole of microsporidial keratoconjunctivitis among immunocompromised individuals with HIV/AIDS. METHODS: This is a retrospective case series. Diagnosis of microsporid...

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Autores principales: Taju, Sadik, Tilahun, Yonas, Ayalew, Menen, Fikrie, Nigus, Schneider, Jakob, Kempen, John H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170099/
https://www.ncbi.nlm.nih.gov/pubmed/21559864
http://dx.doi.org/10.1007/s12348-011-0025-y
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author Taju, Sadik
Tilahun, Yonas
Ayalew, Menen
Fikrie, Nigus
Schneider, Jakob
Kempen, John H.
author_facet Taju, Sadik
Tilahun, Yonas
Ayalew, Menen
Fikrie, Nigus
Schneider, Jakob
Kempen, John H.
author_sort Taju, Sadik
collection PubMed
description PURPOSE: The purpose of this study is to describe the clinical characteristics, microscopic findings, and treatment response to albendazole of microsporidial keratoconjunctivitis among immunocompromised individuals with HIV/AIDS. METHODS: This is a retrospective case series. Diagnosis of microsporidial keratoconjunctivitis was confirmed by subspecialist examination and conjunctival swabs examined by light microscopy. HIV infection was documented, and absolute CD4+ T cell count was determined. Patients were treated with albendazole and followed for clinical response. RESULTS: Light microscopy from the conjunctival swabs demonstrated myriad small, round to oval microsporidial organisms that stained positively with modified acid-fast methods. Two of the patients initially not taking highly active antiretroviral therapy (HAART) and presenting with an absolute CD4+ T cell count less than 100 cells/μL had a more severe form of keratoconjunctivitis than the third patient (receiving HAART, with a CD4+ T cell count of 259 cells/μL). All patients were started or continued on HAART. Two of the patients responded to oral albendazole, with resolution of symptoms and signs. The third patient did not initially respond, perhaps because of an immune recovery inflammatory syndrome, but subsequently had temporary improvement with albendazole. CONCLUSIONS: Microsporidial keratoconjunctivitis is a rare ocular complication of HIV/AIDS. Light microscopic evaluation of conjunctival swabs may be a useful minimally invasive first step toward diagnosis of microsporidial keratoconjunctivis in settings where electron microscopy is not available. Based on the limited available information, albendazole often is effective for this condition, and is widely available in developing countries at low cost.
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spelling pubmed-31700992011-09-26 Diagnosis and treatment of microsporidial keratoconjunctivitis: literature review and case series Taju, Sadik Tilahun, Yonas Ayalew, Menen Fikrie, Nigus Schneider, Jakob Kempen, John H. J Ophthalmic Inflamm Infect Original Research PURPOSE: The purpose of this study is to describe the clinical characteristics, microscopic findings, and treatment response to albendazole of microsporidial keratoconjunctivitis among immunocompromised individuals with HIV/AIDS. METHODS: This is a retrospective case series. Diagnosis of microsporidial keratoconjunctivitis was confirmed by subspecialist examination and conjunctival swabs examined by light microscopy. HIV infection was documented, and absolute CD4+ T cell count was determined. Patients were treated with albendazole and followed for clinical response. RESULTS: Light microscopy from the conjunctival swabs demonstrated myriad small, round to oval microsporidial organisms that stained positively with modified acid-fast methods. Two of the patients initially not taking highly active antiretroviral therapy (HAART) and presenting with an absolute CD4+ T cell count less than 100 cells/μL had a more severe form of keratoconjunctivitis than the third patient (receiving HAART, with a CD4+ T cell count of 259 cells/μL). All patients were started or continued on HAART. Two of the patients responded to oral albendazole, with resolution of symptoms and signs. The third patient did not initially respond, perhaps because of an immune recovery inflammatory syndrome, but subsequently had temporary improvement with albendazole. CONCLUSIONS: Microsporidial keratoconjunctivitis is a rare ocular complication of HIV/AIDS. Light microscopic evaluation of conjunctival swabs may be a useful minimally invasive first step toward diagnosis of microsporidial keratoconjunctivis in settings where electron microscopy is not available. Based on the limited available information, albendazole often is effective for this condition, and is widely available in developing countries at low cost. Springer-Verlag 2011-05-11 /pmc/articles/PMC3170099/ /pubmed/21559864 http://dx.doi.org/10.1007/s12348-011-0025-y Text en © The Author(s) 2011 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Research
Taju, Sadik
Tilahun, Yonas
Ayalew, Menen
Fikrie, Nigus
Schneider, Jakob
Kempen, John H.
Diagnosis and treatment of microsporidial keratoconjunctivitis: literature review and case series
title Diagnosis and treatment of microsporidial keratoconjunctivitis: literature review and case series
title_full Diagnosis and treatment of microsporidial keratoconjunctivitis: literature review and case series
title_fullStr Diagnosis and treatment of microsporidial keratoconjunctivitis: literature review and case series
title_full_unstemmed Diagnosis and treatment of microsporidial keratoconjunctivitis: literature review and case series
title_short Diagnosis and treatment of microsporidial keratoconjunctivitis: literature review and case series
title_sort diagnosis and treatment of microsporidial keratoconjunctivitis: literature review and case series
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170099/
https://www.ncbi.nlm.nih.gov/pubmed/21559864
http://dx.doi.org/10.1007/s12348-011-0025-y
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