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Eosinophilic fasciitis

Eosinophilic fasciitis is a rare sclerodermiform syndrome of unknown etiology. It is characterized by the thickening of the muscular fascia and subcutaneous tissue, with a variable infiltration of eosinophils. Peripheral eosinophilia, poly or monoclonal hypergammaglobulinemia and increased erythrocy...

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Autores principales: Lamback, Elisa Baranski, Resende, Fernanda Simões Seabra, Lenzi, Thiara Cristina Rocha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324994/
https://www.ncbi.nlm.nih.gov/pubmed/28300895
http://dx.doi.org/10.1590/abd1806-4841.20164683
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author Lamback, Elisa Baranski
Resende, Fernanda Simões Seabra
Lenzi, Thiara Cristina Rocha
author_facet Lamback, Elisa Baranski
Resende, Fernanda Simões Seabra
Lenzi, Thiara Cristina Rocha
author_sort Lamback, Elisa Baranski
collection PubMed
description Eosinophilic fasciitis is a rare sclerodermiform syndrome of unknown etiology. It is characterized by the thickening of the muscular fascia and subcutaneous tissue, with a variable infiltration of eosinophils. Peripheral eosinophilia, poly or monoclonal hypergammaglobulinemia and increased erythrocyte sedimentation rate can be seen. Clinical features begin acutely, with local edema and a painful and symmetrical stiffening of the limbs, progressing rapidly to fibrosis, which can limit joint movements. Some cases have a history of strenuous physical exercise or trauma. The diagnosis is confirmed by a deep skin biopsy. Glucocorticoids in high doses is the treatment of choice. We report a typical eosinophilic fasciitis case with peripheral eosinophilia and dramatic response to pulse therapy with methylprednisolone.
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spelling pubmed-53249942017-03-02 Eosinophilic fasciitis Lamback, Elisa Baranski Resende, Fernanda Simões Seabra Lenzi, Thiara Cristina Rocha An Bras Dermatol Case Report Eosinophilic fasciitis is a rare sclerodermiform syndrome of unknown etiology. It is characterized by the thickening of the muscular fascia and subcutaneous tissue, with a variable infiltration of eosinophils. Peripheral eosinophilia, poly or monoclonal hypergammaglobulinemia and increased erythrocyte sedimentation rate can be seen. Clinical features begin acutely, with local edema and a painful and symmetrical stiffening of the limbs, progressing rapidly to fibrosis, which can limit joint movements. Some cases have a history of strenuous physical exercise or trauma. The diagnosis is confirmed by a deep skin biopsy. Glucocorticoids in high doses is the treatment of choice. We report a typical eosinophilic fasciitis case with peripheral eosinophilia and dramatic response to pulse therapy with methylprednisolone. Sociedade Brasileira de Dermatologia 2016 /pmc/articles/PMC5324994/ /pubmed/28300895 http://dx.doi.org/10.1590/abd1806-4841.20164683 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of 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
Lamback, Elisa Baranski
Resende, Fernanda Simões Seabra
Lenzi, Thiara Cristina Rocha
Eosinophilic fasciitis
title Eosinophilic fasciitis
title_full Eosinophilic fasciitis
title_fullStr Eosinophilic fasciitis
title_full_unstemmed Eosinophilic fasciitis
title_short Eosinophilic fasciitis
title_sort eosinophilic fasciitis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324994/
https://www.ncbi.nlm.nih.gov/pubmed/28300895
http://dx.doi.org/10.1590/abd1806-4841.20164683
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