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Acitretin Treatment for Lipoid Proteinosis

Lipoid proteinosis (LP) is a rare, autosomal-recessive disease characterized by the hoarseness and widespread cutaneous scarring, more prominent on sun-exposed areas. Yellow-white plaques can be seen on oral mucosa and on the skin among depressed scars. Histological evaluation of the affected sites...

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Detalles Bibliográficos
Autores principales: Gündüz, Özgür, Şahiner, Neriman, Atasoy, Pınar, Şenyücel, Çağrı
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3505959/
https://www.ncbi.nlm.nih.gov/pubmed/23259080
http://dx.doi.org/10.1155/2012/324506
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author Gündüz, Özgür
Şahiner, Neriman
Atasoy, Pınar
Şenyücel, Çağrı
author_facet Gündüz, Özgür
Şahiner, Neriman
Atasoy, Pınar
Şenyücel, Çağrı
author_sort Gündüz, Özgür
collection PubMed
description Lipoid proteinosis (LP) is a rare, autosomal-recessive disease characterized by the hoarseness and widespread cutaneous scarring, more prominent on sun-exposed areas. Yellow-white plaques can be seen on oral mucosa and on the skin among depressed scars. Histological evaluation of the affected sites shows accumulation of hyaline-like material in dermis and disruption of basement membrane. Although LP is compatible with normal life expectancy, involvement of upper respiratory tract may endanger patient's life, especially in the case of a respiratory tract infection. Involvement of central nervous system has also been reported, but its clinical importance is obscure. Due to the rarity of LP, a definite therapeutical approach is not established. In this paper we describe a 21-year-old LP patient who was treated with acitretin for six months. Although the outcome with cutaneous lesions was not satisfactory, her hoarseness was significantly improved.
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spelling pubmed-35059592012-12-20 Acitretin Treatment for Lipoid Proteinosis Gündüz, Özgür Şahiner, Neriman Atasoy, Pınar Şenyücel, Çağrı Case Rep Dermatol Med Case Report Lipoid proteinosis (LP) is a rare, autosomal-recessive disease characterized by the hoarseness and widespread cutaneous scarring, more prominent on sun-exposed areas. Yellow-white plaques can be seen on oral mucosa and on the skin among depressed scars. Histological evaluation of the affected sites shows accumulation of hyaline-like material in dermis and disruption of basement membrane. Although LP is compatible with normal life expectancy, involvement of upper respiratory tract may endanger patient's life, especially in the case of a respiratory tract infection. Involvement of central nervous system has also been reported, but its clinical importance is obscure. Due to the rarity of LP, a definite therapeutical approach is not established. In this paper we describe a 21-year-old LP patient who was treated with acitretin for six months. Although the outcome with cutaneous lesions was not satisfactory, her hoarseness was significantly improved. Hindawi Publishing Corporation 2012 2012-08-09 /pmc/articles/PMC3505959/ /pubmed/23259080 http://dx.doi.org/10.1155/2012/324506 Text en Copyright © 2012 Özgür Gündüz 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
Gündüz, Özgür
Şahiner, Neriman
Atasoy, Pınar
Şenyücel, Çağrı
Acitretin Treatment for Lipoid Proteinosis
title Acitretin Treatment for Lipoid Proteinosis
title_full Acitretin Treatment for Lipoid Proteinosis
title_fullStr Acitretin Treatment for Lipoid Proteinosis
title_full_unstemmed Acitretin Treatment for Lipoid Proteinosis
title_short Acitretin Treatment for Lipoid Proteinosis
title_sort acitretin treatment for lipoid proteinosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3505959/
https://www.ncbi.nlm.nih.gov/pubmed/23259080
http://dx.doi.org/10.1155/2012/324506
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