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Scleredema associated with Sjögren’s syndrome

Scleredema adultorum of Buschke is a rare disorder characterized by diffuse swelling and non-pitting induration of the skin usually involving the face, neck, arms and upper trunk. It has been associated with previous infectious diseases, diabetes, paraproteinemia and, more rarely, malignant neoplasm...

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Autores principales: Alves, João, Judas, Tiago, Ferreira, Tiago, Matos, Diogo, Bártolo, Elvira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4540515/
https://www.ncbi.nlm.nih.gov/pubmed/26312681
http://dx.doi.org/10.1590/abd1806-4841.20153779
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author Alves, João
Judas, Tiago
Ferreira, Tiago
Matos, Diogo
Bártolo, Elvira
author_facet Alves, João
Judas, Tiago
Ferreira, Tiago
Matos, Diogo
Bártolo, Elvira
author_sort Alves, João
collection PubMed
description Scleredema adultorum of Buschke is a rare disorder characterized by diffuse swelling and non-pitting induration of the skin usually involving the face, neck, arms and upper trunk. It has been associated with previous infectious diseases, diabetes, paraproteinemia and, more rarely, malignant neoplasms or autoimmune disorders. We report the case of a 30-year-old man who presented with a 2-year history of scleredema. Further investigation led to the diagnosis of primary Sjögren’s syndrome. The association between scleredema and autoimmune disorders has been rarely seen. To our knowledge, there are no other reports describing the association between primary Sjögren’s syndrome and scleredema adultorum of Buschke.
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spelling pubmed-45405152015-08-20 Scleredema associated with Sjögren’s syndrome Alves, João Judas, Tiago Ferreira, Tiago Matos, Diogo Bártolo, Elvira An Bras Dermatol Case Report Scleredema adultorum of Buschke is a rare disorder characterized by diffuse swelling and non-pitting induration of the skin usually involving the face, neck, arms and upper trunk. It has been associated with previous infectious diseases, diabetes, paraproteinemia and, more rarely, malignant neoplasms or autoimmune disorders. We report the case of a 30-year-old man who presented with a 2-year history of scleredema. Further investigation led to the diagnosis of primary Sjögren’s syndrome. The association between scleredema and autoimmune disorders has been rarely seen. To our knowledge, there are no other reports describing the association between primary Sjögren’s syndrome and scleredema adultorum of Buschke. Sociedade Brasileira de Dermatologia 2015 /pmc/articles/PMC4540515/ /pubmed/26312681 http://dx.doi.org/10.1590/abd1806-4841.20153779 Text en © 2015 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
Alves, João
Judas, Tiago
Ferreira, Tiago
Matos, Diogo
Bártolo, Elvira
Scleredema associated with Sjögren’s syndrome
title Scleredema associated with Sjögren’s syndrome
title_full Scleredema associated with Sjögren’s syndrome
title_fullStr Scleredema associated with Sjögren’s syndrome
title_full_unstemmed Scleredema associated with Sjögren’s syndrome
title_short Scleredema associated with Sjögren’s syndrome
title_sort scleredema associated with sjögren’s syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4540515/
https://www.ncbi.nlm.nih.gov/pubmed/26312681
http://dx.doi.org/10.1590/abd1806-4841.20153779
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