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Lipoid proteinosis

Lipoid proteinosis is a rare disorder with autosomal recessive inheritance, characterized by progressive deposition of hyaline material in the skin, mucous membrane, and different organs of the body, resulting in a multitude of clinical manifestations. A 62-year-old male presented with hoarseness of...

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Autores principales: Rao, Roopa Shamsundar, Betkerur, Sunita S, Babu, Chaitanya, Sudha, VM
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162866/
https://www.ncbi.nlm.nih.gov/pubmed/21887007
http://dx.doi.org/10.4103/0973-029X.57675
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author Rao, Roopa Shamsundar
Betkerur, Sunita S
Babu, Chaitanya
Sudha, VM
author_facet Rao, Roopa Shamsundar
Betkerur, Sunita S
Babu, Chaitanya
Sudha, VM
author_sort Rao, Roopa Shamsundar
collection PubMed
description Lipoid proteinosis is a rare disorder with autosomal recessive inheritance, characterized by progressive deposition of hyaline material in the skin, mucous membrane, and different organs of the body, resulting in a multitude of clinical manifestations. A 62-year-old male presented with hoarseness of voice since infancy, eyelid beading, and generalized acneiform scars on the facial skin and extremities, and yellowish papules on his tongue and buccal mucose. The patient was diagnosed clinically as a case of Lipoid proteinosis, which was confirmed by skin and mucosal biopsy. The objective of the present work is to describe this rare entity, with approximately 250 cases found in medical literature. This case report also illustrates that Lipoid proteinosis may show protean clinical features and yet may remain undiagnosed for many years. This report will hopefully spawn further studies that will lead to early diagnosis.
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spelling pubmed-31628662011-09-01 Lipoid proteinosis Rao, Roopa Shamsundar Betkerur, Sunita S Babu, Chaitanya Sudha, VM J Oral Maxillofac Pathol Case Report Lipoid proteinosis is a rare disorder with autosomal recessive inheritance, characterized by progressive deposition of hyaline material in the skin, mucous membrane, and different organs of the body, resulting in a multitude of clinical manifestations. A 62-year-old male presented with hoarseness of voice since infancy, eyelid beading, and generalized acneiform scars on the facial skin and extremities, and yellowish papules on his tongue and buccal mucose. The patient was diagnosed clinically as a case of Lipoid proteinosis, which was confirmed by skin and mucosal biopsy. The objective of the present work is to describe this rare entity, with approximately 250 cases found in medical literature. This case report also illustrates that Lipoid proteinosis may show protean clinical features and yet may remain undiagnosed for many years. This report will hopefully spawn further studies that will lead to early diagnosis. Medknow Publications 2009 /pmc/articles/PMC3162866/ /pubmed/21887007 http://dx.doi.org/10.4103/0973-029X.57675 Text en © Journal of Oral and Maxillofacial Pathology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Rao, Roopa Shamsundar
Betkerur, Sunita S
Babu, Chaitanya
Sudha, VM
Lipoid proteinosis
title Lipoid proteinosis
title_full Lipoid proteinosis
title_fullStr Lipoid proteinosis
title_full_unstemmed Lipoid proteinosis
title_short Lipoid proteinosis
title_sort lipoid proteinosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162866/
https://www.ncbi.nlm.nih.gov/pubmed/21887007
http://dx.doi.org/10.4103/0973-029X.57675
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