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Localized scleroderma: clinical spectrum and therapeutic update()

Scleroderma is a rare connective tissue disease that is manifested by cutaneous sclerosis and variable systemic involvement. Two categories of scleroderma are known: systemic sclerosis, characterized by cutaneous sclerosis and visceral involvement, and localized scleroderma or morphea which classica...

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Detalles Bibliográficos
Autores principales: Careta, Mariana Figueiroa, Romiti, Ricardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323700/
https://www.ncbi.nlm.nih.gov/pubmed/25672301
http://dx.doi.org/10.1590/abd1806-4841.20152890
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author Careta, Mariana Figueiroa
Romiti, Ricardo
author_facet Careta, Mariana Figueiroa
Romiti, Ricardo
author_sort Careta, Mariana Figueiroa
collection PubMed
description Scleroderma is a rare connective tissue disease that is manifested by cutaneous sclerosis and variable systemic involvement. Two categories of scleroderma are known: systemic sclerosis, characterized by cutaneous sclerosis and visceral involvement, and localized scleroderma or morphea which classically presents benign and self-limited evolution and is confined to the skin and/or underlying tissues. Localized scleroderma is a rare disease of unknown etiology. Recent studies show that the localized form may affect internal organs and have variable morbidity. Treatment should be started very early, before complications occur due to the high morbidity of localized scleroderma. In this review, we report the most important aspects and particularities in the treatment of patients diagnosed with localized scleroderma.
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spelling pubmed-43237002015-02-20 Localized scleroderma: clinical spectrum and therapeutic update() Careta, Mariana Figueiroa Romiti, Ricardo An Bras Dermatol Review Scleroderma is a rare connective tissue disease that is manifested by cutaneous sclerosis and variable systemic involvement. Two categories of scleroderma are known: systemic sclerosis, characterized by cutaneous sclerosis and visceral involvement, and localized scleroderma or morphea which classically presents benign and self-limited evolution and is confined to the skin and/or underlying tissues. Localized scleroderma is a rare disease of unknown etiology. Recent studies show that the localized form may affect internal organs and have variable morbidity. Treatment should be started very early, before complications occur due to the high morbidity of localized scleroderma. In this review, we report the most important aspects and particularities in the treatment of patients diagnosed with localized scleroderma. Sociedade Brasileira de Dermatologia 2015 /pmc/articles/PMC4323700/ /pubmed/25672301 http://dx.doi.org/10.1590/abd1806-4841.20152890 Text en ©2015 by Anais Brasileiros de Dermatologia http://creativecommons.org/licenses/by-nc/3.0/ 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 Review
Careta, Mariana Figueiroa
Romiti, Ricardo
Localized scleroderma: clinical spectrum and therapeutic update()
title Localized scleroderma: clinical spectrum and therapeutic update()
title_full Localized scleroderma: clinical spectrum and therapeutic update()
title_fullStr Localized scleroderma: clinical spectrum and therapeutic update()
title_full_unstemmed Localized scleroderma: clinical spectrum and therapeutic update()
title_short Localized scleroderma: clinical spectrum and therapeutic update()
title_sort localized scleroderma: clinical spectrum and therapeutic update()
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323700/
https://www.ncbi.nlm.nih.gov/pubmed/25672301
http://dx.doi.org/10.1590/abd1806-4841.20152890
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