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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications
2009
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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. |
format | Online Article Text |
id | pubmed-3162866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT raoroopashamsundar lipoidproteinosis AT betkerursunitas lipoidproteinosis AT babuchaitanya lipoidproteinosis AT sudhavm lipoidproteinosis |