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Eosinophilic Fasciitis Responds Well to Steroids and Methotrexate

Eosinophilic fasciitis (EF) is a rare systemic inflammatory disease with an unknown etiology. Making a diagnosis in such a case is always a challenge as it is a rare disease and mimics scleroderma and scleroderma-like syndrome but should be kept in mind as it carries a high mortality. Furthermore, i...

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Autores principales: Mahdi, Asmaa Sabr, Nasr, Iman H., Al Jahdhami, Suad, Kamona, Atheel, Al Wahshi, Humaid A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: OMJ 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851076/
https://www.ncbi.nlm.nih.gov/pubmed/31745423
http://dx.doi.org/10.5001/omj.2019.102
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author Mahdi, Asmaa Sabr
Nasr, Iman H.
Al Jahdhami, Suad
Kamona, Atheel
Al Wahshi, Humaid A.
author_facet Mahdi, Asmaa Sabr
Nasr, Iman H.
Al Jahdhami, Suad
Kamona, Atheel
Al Wahshi, Humaid A.
author_sort Mahdi, Asmaa Sabr
collection PubMed
description Eosinophilic fasciitis (EF) is a rare systemic inflammatory disease with an unknown etiology. Making a diagnosis in such a case is always a challenge as it is a rare disease and mimics scleroderma and scleroderma-like syndrome but should be kept in mind as it carries a high mortality. Furthermore, it is a treatable disease. Here, we report a 41-year-old woman who presented to the rheumatology clinic at the Royal Hospital, Muscat, Oman, with a one-month history of bilateral swelling of the forearms along with skin tightness and fingers contraction. Her history and physical examination along with histopathological examination and magnetic resonance imaging findings were consistent with EF. She showed an excellent response to steroids and methotrexate which is not a combination therapy that has been tried or mentioned previously.
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spelling pubmed-68510762019-11-19 Eosinophilic Fasciitis Responds Well to Steroids and Methotrexate Mahdi, Asmaa Sabr Nasr, Iman H. Al Jahdhami, Suad Kamona, Atheel Al Wahshi, Humaid A. Oman Med J Case Report Eosinophilic fasciitis (EF) is a rare systemic inflammatory disease with an unknown etiology. Making a diagnosis in such a case is always a challenge as it is a rare disease and mimics scleroderma and scleroderma-like syndrome but should be kept in mind as it carries a high mortality. Furthermore, it is a treatable disease. Here, we report a 41-year-old woman who presented to the rheumatology clinic at the Royal Hospital, Muscat, Oman, with a one-month history of bilateral swelling of the forearms along with skin tightness and fingers contraction. Her history and physical examination along with histopathological examination and magnetic resonance imaging findings were consistent with EF. She showed an excellent response to steroids and methotrexate which is not a combination therapy that has been tried or mentioned previously. OMJ 2019-11 /pmc/articles/PMC6851076/ /pubmed/31745423 http://dx.doi.org/10.5001/omj.2019.102 Text en The OMJ is Published Bimonthly and Copyrighted 2019 by the OMSB. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC) 4.0 License. http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Case Report
Mahdi, Asmaa Sabr
Nasr, Iman H.
Al Jahdhami, Suad
Kamona, Atheel
Al Wahshi, Humaid A.
Eosinophilic Fasciitis Responds Well to Steroids and Methotrexate
title Eosinophilic Fasciitis Responds Well to Steroids and Methotrexate
title_full Eosinophilic Fasciitis Responds Well to Steroids and Methotrexate
title_fullStr Eosinophilic Fasciitis Responds Well to Steroids and Methotrexate
title_full_unstemmed Eosinophilic Fasciitis Responds Well to Steroids and Methotrexate
title_short Eosinophilic Fasciitis Responds Well to Steroids and Methotrexate
title_sort eosinophilic fasciitis responds well to steroids and methotrexate
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851076/
https://www.ncbi.nlm.nih.gov/pubmed/31745423
http://dx.doi.org/10.5001/omj.2019.102
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