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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...

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Autores principales: Gdynia, H-J, Weydt, P, Ernst, A, Klein, S, Sperfeld, A-D, Riecker, A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2009
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.
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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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