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Olmsted Syndrome

Olmsted syndrome is a rare congenital, sharply circumscribed transgredient palmoplantar keratoderma. It was first described by Olmsted in 1927. The diagnosis of this rare disease depends on clinical features like symmetrical involvement of keratoderma of the palms and soles and the symmetrical hyper...

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Autores principales: Elise Tonoli, Renata, De Villa, Damiê, Hübner Frainer, Renata, Pizzarro Meneghello, Luana, Ricachnevsky, Nelson, de Quadros, Maurício
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3540698/
https://www.ncbi.nlm.nih.gov/pubmed/23320205
http://dx.doi.org/10.1155/2012/927305
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author Elise Tonoli, Renata
De Villa, Damiê
Hübner Frainer, Renata
Pizzarro Meneghello, Luana
Ricachnevsky, Nelson
de Quadros, Maurício
author_facet Elise Tonoli, Renata
De Villa, Damiê
Hübner Frainer, Renata
Pizzarro Meneghello, Luana
Ricachnevsky, Nelson
de Quadros, Maurício
author_sort Elise Tonoli, Renata
collection PubMed
description Olmsted syndrome is a rare congenital, sharply circumscribed transgredient palmoplantar keratoderma. It was first described by Olmsted in 1927. The diagnosis of this rare disease depends on clinical features like symmetrical involvement of keratoderma of the palms and soles and the symmetrical hyperkeratotic plaques around the body orifices. It starts in the neonatal period or in childhood. The disease has a slow but progressive and extremely disabling course. Treatment of Olmsted syndrome is often based on topical therapy with retinoic acid, corticosteroid, emollients, and keratolytics. The present paper describes a case of Olmsted syndrome and its treatment.
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spelling pubmed-35406982013-01-14 Olmsted Syndrome Elise Tonoli, Renata De Villa, Damiê Hübner Frainer, Renata Pizzarro Meneghello, Luana Ricachnevsky, Nelson de Quadros, Maurício Case Rep Dermatol Med Case Report Olmsted syndrome is a rare congenital, sharply circumscribed transgredient palmoplantar keratoderma. It was first described by Olmsted in 1927. The diagnosis of this rare disease depends on clinical features like symmetrical involvement of keratoderma of the palms and soles and the symmetrical hyperkeratotic plaques around the body orifices. It starts in the neonatal period or in childhood. The disease has a slow but progressive and extremely disabling course. Treatment of Olmsted syndrome is often based on topical therapy with retinoic acid, corticosteroid, emollients, and keratolytics. The present paper describes a case of Olmsted syndrome and its treatment. Hindawi Publishing Corporation 2012 2012-12-23 /pmc/articles/PMC3540698/ /pubmed/23320205 http://dx.doi.org/10.1155/2012/927305 Text en Copyright © 2012 Renata Elise Tonoli et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under 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
Elise Tonoli, Renata
De Villa, Damiê
Hübner Frainer, Renata
Pizzarro Meneghello, Luana
Ricachnevsky, Nelson
de Quadros, Maurício
Olmsted Syndrome
title Olmsted Syndrome
title_full Olmsted Syndrome
title_fullStr Olmsted Syndrome
title_full_unstemmed Olmsted Syndrome
title_short Olmsted Syndrome
title_sort olmsted syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3540698/
https://www.ncbi.nlm.nih.gov/pubmed/23320205
http://dx.doi.org/10.1155/2012/927305
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