Bullous systemic lupus erythematosus in a 10-year-old child

Bullous systemic lupus erythematosus (BSLE) is a rare autoimmune subepidermal blistering disease, with few cases described in childhood. It has different clinical-pathological features. We report a case of BSLE in a 10-year-old child with systemic lupus erythematosus, treated with prednisone and hyd...

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Autores principales: Hans-Bittner, Nelise Ritter, Bittner, Guilherme Canho, Hans Filho, Günter, Takita, Luiz Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726672/
https://www.ncbi.nlm.nih.gov/pubmed/29267441
http://dx.doi.org/10.1590/abd1806-4841.20176074
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author Hans-Bittner, Nelise Ritter
Bittner, Guilherme Canho
Hans Filho, Günter
Takita, Luiz Carlos
author_facet Hans-Bittner, Nelise Ritter
Bittner, Guilherme Canho
Hans Filho, Günter
Takita, Luiz Carlos
author_sort Hans-Bittner, Nelise Ritter
collection PubMed
description Bullous systemic lupus erythematosus (BSLE) is a rare autoimmune subepidermal blistering disease, with few cases described in childhood. It has different clinical-pathological features. We report a case of BSLE in a 10-year-old child with systemic lupus erythematosus, treated with prednisone and hydroxychloroquine. There was complete remission with dapsone, with no recurrence of skin lesions throughout one year of follow-up. We highlight the rarity and early age of occurrence.
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spelling pubmed-57266722017-12-18 Bullous systemic lupus erythematosus in a 10-year-old child Hans-Bittner, Nelise Ritter Bittner, Guilherme Canho Hans Filho, Günter Takita, Luiz Carlos An Bras Dermatol Case Report Bullous systemic lupus erythematosus (BSLE) is a rare autoimmune subepidermal blistering disease, with few cases described in childhood. It has different clinical-pathological features. We report a case of BSLE in a 10-year-old child with systemic lupus erythematosus, treated with prednisone and hydroxychloroquine. There was complete remission with dapsone, with no recurrence of skin lesions throughout one year of follow-up. We highlight the rarity and early age of occurrence. Sociedade Brasileira de Dermatologia 2017 /pmc/articles/PMC5726672/ /pubmed/29267441 http://dx.doi.org/10.1590/abd1806-4841.20176074 Text en ©2017 by Anais Brasileiros de Dermatologia http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium provided the original work is properly cited.
spellingShingle Case Report
Hans-Bittner, Nelise Ritter
Bittner, Guilherme Canho
Hans Filho, Günter
Takita, Luiz Carlos
Bullous systemic lupus erythematosus in a 10-year-old child
title Bullous systemic lupus erythematosus in a 10-year-old child
title_full Bullous systemic lupus erythematosus in a 10-year-old child
title_fullStr Bullous systemic lupus erythematosus in a 10-year-old child
title_full_unstemmed Bullous systemic lupus erythematosus in a 10-year-old child
title_short Bullous systemic lupus erythematosus in a 10-year-old child
title_sort bullous systemic lupus erythematosus in a 10-year-old child
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726672/
https://www.ncbi.nlm.nih.gov/pubmed/29267441
http://dx.doi.org/10.1590/abd1806-4841.20176074
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