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Oral lesions associated with nevirapine-related Stevens Johnson syndrome: A report of four cases
Nevirapine is a non-nucleoside reverse transcriptase inhibitor, widely used in combination with other antiretroviral agents for treatment of HIV infection. Steven Johnson syndrome (SJS) is the major toxicity of nevirapine. We describe here four cases of SJS in HIV seropositive patients following nev...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125654/ https://www.ncbi.nlm.nih.gov/pubmed/21731276 http://dx.doi.org/10.4103/0973-029X.80024 |
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author | Balasundaram, S Ranganathan, K Umadevi, K Gunaseelan, R Kumaraswamy, N Solomon, Sunithi Devaleenol, Bella Ambrose, Pradeep |
author_facet | Balasundaram, S Ranganathan, K Umadevi, K Gunaseelan, R Kumaraswamy, N Solomon, Sunithi Devaleenol, Bella Ambrose, Pradeep |
author_sort | Balasundaram, S |
collection | PubMed |
description | Nevirapine is a non-nucleoside reverse transcriptase inhibitor, widely used in combination with other antiretroviral agents for treatment of HIV infection. Steven Johnson syndrome (SJS) is the major toxicity of nevirapine. We describe here four cases of SJS in HIV seropositive patients following nevirapine therapy. In all four cases cutaneous hypersensitivity reaction was seen with extreme oral lesions, three patients presented clinically with elevated liver enzymes and hepatitis, and two patients had ocular involvement. |
format | Online Article Text |
id | pubmed-3125654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-31256542011-07-01 Oral lesions associated with nevirapine-related Stevens Johnson syndrome: A report of four cases Balasundaram, S Ranganathan, K Umadevi, K Gunaseelan, R Kumaraswamy, N Solomon, Sunithi Devaleenol, Bella Ambrose, Pradeep J Oral Maxillofac Pathol Case Report Nevirapine is a non-nucleoside reverse transcriptase inhibitor, widely used in combination with other antiretroviral agents for treatment of HIV infection. Steven Johnson syndrome (SJS) is the major toxicity of nevirapine. We describe here four cases of SJS in HIV seropositive patients following nevirapine therapy. In all four cases cutaneous hypersensitivity reaction was seen with extreme oral lesions, three patients presented clinically with elevated liver enzymes and hepatitis, and two patients had ocular involvement. Medknow Publications 2011 /pmc/articles/PMC3125654/ /pubmed/21731276 http://dx.doi.org/10.4103/0973-029X.80024 Text en © Journal of Oral and Maxillofacial Pathology http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Balasundaram, S Ranganathan, K Umadevi, K Gunaseelan, R Kumaraswamy, N Solomon, Sunithi Devaleenol, Bella Ambrose, Pradeep Oral lesions associated with nevirapine-related Stevens Johnson syndrome: A report of four cases |
title | Oral lesions associated with nevirapine-related Stevens Johnson syndrome: A report of four cases |
title_full | Oral lesions associated with nevirapine-related Stevens Johnson syndrome: A report of four cases |
title_fullStr | Oral lesions associated with nevirapine-related Stevens Johnson syndrome: A report of four cases |
title_full_unstemmed | Oral lesions associated with nevirapine-related Stevens Johnson syndrome: A report of four cases |
title_short | Oral lesions associated with nevirapine-related Stevens Johnson syndrome: A report of four cases |
title_sort | oral lesions associated with nevirapine-related stevens johnson syndrome: a report of four cases |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125654/ https://www.ncbi.nlm.nih.gov/pubmed/21731276 http://dx.doi.org/10.4103/0973-029X.80024 |
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