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Imiquimod-induced bullous pemphigoid: A case report
A 72-year-old man treated with 3.5% imiquimod cream for scalp actinic keratoses developed the usual crusted and erosive reaction but developed bullae on the scalp, as well as the limbs and torso after several weeks into treatment. Biopsy confirmed bullous pemphigoid. He was treated with clobetasol o...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10071145/ https://www.ncbi.nlm.nih.gov/pubmed/37025248 http://dx.doi.org/10.1177/2050313X231164222 |
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author | Li, Heidi Oi-Yee Aw, Michael Glassman, Steven J |
author_facet | Li, Heidi Oi-Yee Aw, Michael Glassman, Steven J |
author_sort | Li, Heidi Oi-Yee |
collection | PubMed |
description | A 72-year-old man treated with 3.5% imiquimod cream for scalp actinic keratoses developed the usual crusted and erosive reaction but developed bullae on the scalp, as well as the limbs and torso after several weeks into treatment. Biopsy confirmed bullous pemphigoid. He was treated with clobetasol ointment, prednisone and methotrexate, with eventual disease control. He had a severe disease course. Bullous pemphigoid is usually idiopathic, but can be induced by skin trauma, as well as by several medications; this is the first report of imiquimod as a trigger. Imiquimod is a toll-like receptor 7 agonist that induces cellular apoptosis and recruits pro-inflammatory cytokines including tumour necrosis factor-alpha and interferon-alpha, which have been implicated in autoimmunity. This case highlights an unusual but severe adverse effect from topical imiquimod. |
format | Online Article Text |
id | pubmed-10071145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-100711452023-04-05 Imiquimod-induced bullous pemphigoid: A case report Li, Heidi Oi-Yee Aw, Michael Glassman, Steven J SAGE Open Med Case Rep JCMS Case Report A 72-year-old man treated with 3.5% imiquimod cream for scalp actinic keratoses developed the usual crusted and erosive reaction but developed bullae on the scalp, as well as the limbs and torso after several weeks into treatment. Biopsy confirmed bullous pemphigoid. He was treated with clobetasol ointment, prednisone and methotrexate, with eventual disease control. He had a severe disease course. Bullous pemphigoid is usually idiopathic, but can be induced by skin trauma, as well as by several medications; this is the first report of imiquimod as a trigger. Imiquimod is a toll-like receptor 7 agonist that induces cellular apoptosis and recruits pro-inflammatory cytokines including tumour necrosis factor-alpha and interferon-alpha, which have been implicated in autoimmunity. This case highlights an unusual but severe adverse effect from topical imiquimod. SAGE Publications 2023-03-30 /pmc/articles/PMC10071145/ /pubmed/37025248 http://dx.doi.org/10.1177/2050313X231164222 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | JCMS Case Report Li, Heidi Oi-Yee Aw, Michael Glassman, Steven J Imiquimod-induced bullous pemphigoid: A case report |
title | Imiquimod-induced bullous pemphigoid: A case report |
title_full | Imiquimod-induced bullous pemphigoid: A case report |
title_fullStr | Imiquimod-induced bullous pemphigoid: A case report |
title_full_unstemmed | Imiquimod-induced bullous pemphigoid: A case report |
title_short | Imiquimod-induced bullous pemphigoid: A case report |
title_sort | imiquimod-induced bullous pemphigoid: a case report |
topic | JCMS Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10071145/ https://www.ncbi.nlm.nih.gov/pubmed/37025248 http://dx.doi.org/10.1177/2050313X231164222 |
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