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Myositis associated with localized lipodystrophy: an unrecognized condition?
Lipodystrophies represent a heterogeneous group of diseases characterized by altered body fat repartition and often metabolic alterations. Here we illustrate a 20 year old male with myositis in association with localized lipodystrophy. Immunohistochemical stainings revealed a regular pattern of dyst...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3351983/ https://www.ncbi.nlm.nih.gov/pubmed/19541581 http://dx.doi.org/10.1186/2047-783X-14-5-228 |
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author | Gdynia, H-J Weydt, P Ernst, A Klein, S Sperfeld, A-D Riecker, A |
author_facet | Gdynia, H-J Weydt, P Ernst, A Klein, S Sperfeld, A-D Riecker, A |
author_sort | Gdynia, H-J |
collection | PubMed |
description | Lipodystrophies represent a heterogeneous group of diseases characterized by altered body fat repartition and often metabolic alterations. Here we illustrate a 20 year old male with myositis in association with localized lipodystrophy. Immunohistochemical stainings revealed a regular pattern of dystrophin, dysferlin, sarcoglycans, and theletonin. Furtermore, there was no evidence of Lamin A/C deficiency. A nearly identical clinical and histological picture has been described in three patients up to now. Although it is difficult to speculate on a causative pathophysiological mechanism at this time, it is possible that this association represents an unrecognized condition. |
format | Online Article Text |
id | pubmed-3351983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33519832012-05-16 Myositis associated with localized lipodystrophy: an unrecognized condition? Gdynia, H-J Weydt, P Ernst, A Klein, S Sperfeld, A-D Riecker, A Eur J Med Res Case Report Lipodystrophies represent a heterogeneous group of diseases characterized by altered body fat repartition and often metabolic alterations. Here we illustrate a 20 year old male with myositis in association with localized lipodystrophy. Immunohistochemical stainings revealed a regular pattern of dystrophin, dysferlin, sarcoglycans, and theletonin. Furtermore, there was no evidence of Lamin A/C deficiency. A nearly identical clinical and histological picture has been described in three patients up to now. Although it is difficult to speculate on a causative pathophysiological mechanism at this time, it is possible that this association represents an unrecognized condition. BioMed Central 2009-05-14 /pmc/articles/PMC3351983/ /pubmed/19541581 http://dx.doi.org/10.1186/2047-783X-14-5-228 Text en Copyright ©2009 I. Holzapfel Publishers |
spellingShingle | Case Report Gdynia, H-J Weydt, P Ernst, A Klein, S Sperfeld, A-D Riecker, A Myositis associated with localized lipodystrophy: an unrecognized condition? |
title | Myositis associated with localized lipodystrophy: an unrecognized condition? |
title_full | Myositis associated with localized lipodystrophy: an unrecognized condition? |
title_fullStr | Myositis associated with localized lipodystrophy: an unrecognized condition? |
title_full_unstemmed | Myositis associated with localized lipodystrophy: an unrecognized condition? |
title_short | Myositis associated with localized lipodystrophy: an unrecognized condition? |
title_sort | myositis associated with localized lipodystrophy: an unrecognized condition? |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3351983/ https://www.ncbi.nlm.nih.gov/pubmed/19541581 http://dx.doi.org/10.1186/2047-783X-14-5-228 |
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