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Vancomycin-associated linear IgA disease mimicking toxic epidermal necrolysis

Linear IgA dermatosis is a rare subepidermal autoimmune blistering disease characterized by linear deposition of IgA along the basement membrane zone. In the last three decades, many different drugs have been associated with the drug-induced form of the disease, especially vancomycin. We report a ca...

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Autores principales: Pereira, Amanda Regio, de Moura, Luis Henrique Barbizan, Pinheiro, Jhonatan Rafael Siqueira, Pasin, Victor Pavan, Enokihara, Milvia Maria Simões e Silva, Porro, Adriana Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324987/
https://www.ncbi.nlm.nih.gov/pubmed/28300888
http://dx.doi.org/10.1590/abd1806-4841.20164665
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author Pereira, Amanda Regio
de Moura, Luis Henrique Barbizan
Pinheiro, Jhonatan Rafael Siqueira
Pasin, Victor Pavan
Enokihara, Milvia Maria Simões e Silva
Porro, Adriana Maria
author_facet Pereira, Amanda Regio
de Moura, Luis Henrique Barbizan
Pinheiro, Jhonatan Rafael Siqueira
Pasin, Victor Pavan
Enokihara, Milvia Maria Simões e Silva
Porro, Adriana Maria
author_sort Pereira, Amanda Regio
collection PubMed
description Linear IgA dermatosis is a rare subepidermal autoimmune blistering disease characterized by linear deposition of IgA along the basement membrane zone. In the last three decades, many different drugs have been associated with the drug-induced form of the disease, especially vancomycin. We report a case of vancomycin-induced linear IgA disease mimicking toxic epidermal necrolysis. The aim of this work is to emphasize the need to include this differential diagnosis in cases of epidermal detachment and to review the literature on the subject and this specific clinical presentation.
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spelling pubmed-53249872017-03-02 Vancomycin-associated linear IgA disease mimicking toxic epidermal necrolysis Pereira, Amanda Regio de Moura, Luis Henrique Barbizan Pinheiro, Jhonatan Rafael Siqueira Pasin, Victor Pavan Enokihara, Milvia Maria Simões e Silva Porro, Adriana Maria An Bras Dermatol Case Report Linear IgA dermatosis is a rare subepidermal autoimmune blistering disease characterized by linear deposition of IgA along the basement membrane zone. In the last three decades, many different drugs have been associated with the drug-induced form of the disease, especially vancomycin. We report a case of vancomycin-induced linear IgA disease mimicking toxic epidermal necrolysis. The aim of this work is to emphasize the need to include this differential diagnosis in cases of epidermal detachment and to review the literature on the subject and this specific clinical presentation. Sociedade Brasileira de Dermatologia 2016 /pmc/articles/PMC5324987/ /pubmed/28300888 http://dx.doi.org/10.1590/abd1806-4841.20164665 Text en http://creativecommons.org/licenses/by/4.0/ 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
Pereira, Amanda Regio
de Moura, Luis Henrique Barbizan
Pinheiro, Jhonatan Rafael Siqueira
Pasin, Victor Pavan
Enokihara, Milvia Maria Simões e Silva
Porro, Adriana Maria
Vancomycin-associated linear IgA disease mimicking toxic epidermal necrolysis
title Vancomycin-associated linear IgA disease mimicking toxic epidermal necrolysis
title_full Vancomycin-associated linear IgA disease mimicking toxic epidermal necrolysis
title_fullStr Vancomycin-associated linear IgA disease mimicking toxic epidermal necrolysis
title_full_unstemmed Vancomycin-associated linear IgA disease mimicking toxic epidermal necrolysis
title_short Vancomycin-associated linear IgA disease mimicking toxic epidermal necrolysis
title_sort vancomycin-associated linear iga disease mimicking toxic epidermal necrolysis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324987/
https://www.ncbi.nlm.nih.gov/pubmed/28300888
http://dx.doi.org/10.1590/abd1806-4841.20164665
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