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Bullous disorders as a manifestation of immune reconstitution inflammatory syndrome: A series of three cases

Bullous disorders such as pemphigus vulgaris, bullous pemphigoid after the initiation of highly active antiretroviral therapy in certain human immunodeficiency virus reactive individuals have been described in this case series as a manifestation of an immune reconstitution inflammatory syndrome. Thi...

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Detalles Bibliográficos
Autores principales: Das, Rama, Sarkar, Somenath, Besra, Mrinal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841664/
https://www.ncbi.nlm.nih.gov/pubmed/24339465
http://dx.doi.org/10.4103/2589-0557.120552
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author Das, Rama
Sarkar, Somenath
Besra, Mrinal
author_facet Das, Rama
Sarkar, Somenath
Besra, Mrinal
author_sort Das, Rama
collection PubMed
description Bullous disorders such as pemphigus vulgaris, bullous pemphigoid after the initiation of highly active antiretroviral therapy in certain human immunodeficiency virus reactive individuals have been described in this case series as a manifestation of an immune reconstitution inflammatory syndrome. This phenomenon should be suspected in individuals who present with bullous lesions within 3-8 weeks after initiation of therapy despite of improved immunological response. Strong clinical suspicion, through clinical examination, appropriate laboratory investigation such as CD4 T-cell count, histopathological examinations with H and E stain, direct immunofluorescence test are required for diagnosis.
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spelling pubmed-38416642013-12-11 Bullous disorders as a manifestation of immune reconstitution inflammatory syndrome: A series of three cases Das, Rama Sarkar, Somenath Besra, Mrinal Indian J Sex Transm Dis AIDS Case Report Bullous disorders such as pemphigus vulgaris, bullous pemphigoid after the initiation of highly active antiretroviral therapy in certain human immunodeficiency virus reactive individuals have been described in this case series as a manifestation of an immune reconstitution inflammatory syndrome. This phenomenon should be suspected in individuals who present with bullous lesions within 3-8 weeks after initiation of therapy despite of improved immunological response. Strong clinical suspicion, through clinical examination, appropriate laboratory investigation such as CD4 T-cell count, histopathological examinations with H and E stain, direct immunofluorescence test are required for diagnosis. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3841664/ /pubmed/24339465 http://dx.doi.org/10.4103/2589-0557.120552 Text en Copyright: © Indian Journal of Sexually Transmitted Diseases and AIDS http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Das, Rama
Sarkar, Somenath
Besra, Mrinal
Bullous disorders as a manifestation of immune reconstitution inflammatory syndrome: A series of three cases
title Bullous disorders as a manifestation of immune reconstitution inflammatory syndrome: A series of three cases
title_full Bullous disorders as a manifestation of immune reconstitution inflammatory syndrome: A series of three cases
title_fullStr Bullous disorders as a manifestation of immune reconstitution inflammatory syndrome: A series of three cases
title_full_unstemmed Bullous disorders as a manifestation of immune reconstitution inflammatory syndrome: A series of three cases
title_short Bullous disorders as a manifestation of immune reconstitution inflammatory syndrome: A series of three cases
title_sort bullous disorders as a manifestation of immune reconstitution inflammatory syndrome: a series of three cases
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841664/
https://www.ncbi.nlm.nih.gov/pubmed/24339465
http://dx.doi.org/10.4103/2589-0557.120552
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