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A Suspected Case of Silodosin-Induced Erythroderma

An 86-year-old man developed a suspected severe erythroderma during treatment with silodosin (dosage unknown) for benign prostatic enlargement. Two weeks after starting silodosin, he developed a total-body scaling dermatitis. A biopsy was planned but the patient improved at his subsequent visit and...

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Detalles Bibliográficos
Autores principales: Liu, Annie, Giroux, Lyne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4982458/
https://www.ncbi.nlm.nih.gov/pubmed/27747713
http://dx.doi.org/10.1007/s40800-014-0003-z
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author Liu, Annie
Giroux, Lyne
author_facet Liu, Annie
Giroux, Lyne
author_sort Liu, Annie
collection PubMed
description An 86-year-old man developed a suspected severe erythroderma during treatment with silodosin (dosage unknown) for benign prostatic enlargement. Two weeks after starting silodosin, he developed a total-body scaling dermatitis. A biopsy was planned but the patient improved at his subsequent visit and it was not taken. Silodosin was discontinued and the patient received UVB phototherapy, clobetasol ointment, and several bland and protective skin-care measures. One week after the initial presentation, the patient demonstrated improvement in his total-body scaling. Based on these findings, the patient was diagnosed with a suspected silodosin-induced erythroderma. Due to limitations in the patient’s clinical history and investigations, a Naranjo assessment score was not obtainable.
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spelling pubmed-49824582016-08-30 A Suspected Case of Silodosin-Induced Erythroderma Liu, Annie Giroux, Lyne Drug Saf Case Rep Case Report An 86-year-old man developed a suspected severe erythroderma during treatment with silodosin (dosage unknown) for benign prostatic enlargement. Two weeks after starting silodosin, he developed a total-body scaling dermatitis. A biopsy was planned but the patient improved at his subsequent visit and it was not taken. Silodosin was discontinued and the patient received UVB phototherapy, clobetasol ointment, and several bland and protective skin-care measures. One week after the initial presentation, the patient demonstrated improvement in his total-body scaling. Based on these findings, the patient was diagnosed with a suspected silodosin-induced erythroderma. Due to limitations in the patient’s clinical history and investigations, a Naranjo assessment score was not obtainable. Springer International Publishing 2015-02-04 /pmc/articles/PMC4982458/ /pubmed/27747713 http://dx.doi.org/10.1007/s40800-014-0003-z Text en © The Author(s) 2015 https://creativecommons.org/licenses/by-nc/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Case Report
Liu, Annie
Giroux, Lyne
A Suspected Case of Silodosin-Induced Erythroderma
title A Suspected Case of Silodosin-Induced Erythroderma
title_full A Suspected Case of Silodosin-Induced Erythroderma
title_fullStr A Suspected Case of Silodosin-Induced Erythroderma
title_full_unstemmed A Suspected Case of Silodosin-Induced Erythroderma
title_short A Suspected Case of Silodosin-Induced Erythroderma
title_sort suspected case of silodosin-induced erythroderma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4982458/
https://www.ncbi.nlm.nih.gov/pubmed/27747713
http://dx.doi.org/10.1007/s40800-014-0003-z
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