Eosinophilic Fasciitis

Common Name(s)

Eosinophilic Fasciitis

Eosinophilic fasciitis is a very rare condition in which muscle tissue underneath the skin, called fascia, becomes swollen and thick. Rapid swelling can occur in the hands, arms, legs, and feet. People with this condition have a buildup of eosinophils, a type of white blood cell, in the affected fascia and muscles. The exact cause of this condition is unknown. Fewer than 300 cases have been reported in the past 35 years. Eosinophilic fasciitis is similar in appearance to scleroderma but is not related.
 

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How do you compare to others with this condition?

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Eosinophilic Fasciitis" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Eosinophilic Fasciitis" returned 43 free, full-text research articles on human participants. First 3 results:

Eosinophilic fasciitis following allogeneic bone marrow transplantation in a patient with acute myeloid leukaemia.
 

Author(s): Gong-Yao Chu, Hsing-Lin Lin, Gwo-Shing Chen, Ching-Ying Wu

Journal: Acta Derm. Venereol.. 2014 Mar;94(2):221-2.

 

Last Updated: 26 Feb 2014

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Eosinophilic fasciitis.
 

Author(s): Ka Lai Tsoi, Martijn Custers, Liesbeth Bij de Vaate, Johannes W G Jacobs

Journal:

 

A 57-year-old woman presented with malaise and heaviness in her extremities. At first there were no clues of an inflammatory disease, but the patient developed slowly progressive oedema of her arms and legs with induration of the skin. Blood tests showed eosinophilia. Additional analysis ...

Last Updated: 4 Oct 2012

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Generalized morphea developing in a patient previously affected with eosinophilic fasciitis.
 

Author(s): Resham J Vasani, Sudhir V Medhekar

Journal: Indian J Dermatol Venereol Leprol. ;78(5):654-6.

 

Last Updated: 10 Sep 2012

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Eosinophilic Fasciitis" returned 5 free, full-text review articles on human participants. First 3 results:

[Eosinophilic fasciitis].
 

Author(s): Karolina Niklas, Arkadiusz Niklas, Mariusz Puszczewicz

Journal:

 

Eosinophilic fasciitis is a rare connective tissue disease with unclear etiology and pathogenesis. It is classified as a scleroderma-like syndrome. The disease is characterized by fibrosis of the skin and subcutaneous tissues with significant thickening of fascia. Visceral involvement ...

Last Updated: 21 Apr 2015

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Eosinophilic fasciitis: typical abnormalities, variants and differential diagnosis of fasciae abnormalities using MR imaging.
 

Author(s): T Kirchgesner, B Dallaudière, P Omoumi, J Malghem, B Vande Berg, F Lecouvet, F Houssiau, C Galant, A Larbi

Journal: Diagn Interv Imaging. 2015 Apr;96(4):341-8.

 

Eosinophilic fasciitis is a rare condition. It is generally limited to the distal parts of the arms and legs. MRI is the ideal imaging modality for diagnosing and monitoring this condition. MRI findings typically evidence only fascial involvement but on a less regular basis signal ...

Last Updated: 20 Apr 2015

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Eosinophilic fasciitis as a paraneoplastic syndrome, a case report and review of the literature.
 

Author(s): Housam Haddad, Suchitra Sundaram, Cynthia Magro, Usama Gergis

Journal: Hematol Oncol Stem Cell Ther. 2014 Jun;7(2):90-2.

 

Eosinophilic fasciitis (EF) is a rare disease with characteristic clinical and histological features, previously reported to be associated with various hematological and solid malignancies. We report a typical case of eosinophilic fasciitis in a 67-year-old man in association with ...

Last Updated: 9 Jun 2014

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Symptoms, Diagnosis, and Treatment

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There are currently no related results available in Genetic Testing Registry.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

Genotype and Phenotype Correlation in Hereditary Thrombotic Thrombocytopenic Purpura (Upshaw-Schulman Syndrome)
 

Status: Recruiting

Condition Summary: Thrombotic Thrombocytopenic Purpura; Congenital Thrombotic Thrombocytopenic Purpura; Familial Thrombotic Thrombocytopenic Purpura; Thrombotic Thrombocytopenic Purpura, Congenital; Upshaw-Schulman Syndrome

 

Last Updated: 19 Apr 2016

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