Eosinophilic Fasciitis : A Rare Skin Sclerosis
Joint Authors
Côté, Jean-François
Clérici, Thierry
Malines, Caroline
Servy, Amandine
Le Parc, Jean-Marie
Source
Pathology Research International
Issue
Vol. 2011, Issue 2011 (31 Dec. 2011), pp.1-4, 4 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2010-12-01
Country of Publication
Egypt
No. of Pages
4
Main Subjects
Abstract EN
Eosinophilic fasciitis (Schulman's syndrome) is a rare disease with specific clinical symptoms such as the groove sign which facilitate diagnosis.
We report a typical case of eosinophilic fasciitis in an otherwise healthy 49-year-old man who presented with “prayer and groove signs”.
Histological analysis showed sclerosis and eosinophilic infiltration of the fascia.
The patient was successfully treated with systemic corticotherapy and Cyclosporine.
A short review of the clinicopathological features of the lesions is presented.
American Psychological Association (APA)
Servy, Amandine& Clérici, Thierry& Malines, Caroline& Le Parc, Jean-Marie& Côté, Jean-François. 2010. Eosinophilic Fasciitis : A Rare Skin Sclerosis. Pathology Research International،Vol. 2011, no. 2011, pp.1-4.
https://search.emarefa.net/detail/BIM-492951
Modern Language Association (MLA)
Servy, Amandine…[et al.]. Eosinophilic Fasciitis : A Rare Skin Sclerosis. Pathology Research International No. 2011 (2011), pp.1-4.
https://search.emarefa.net/detail/BIM-492951
American Medical Association (AMA)
Servy, Amandine& Clérici, Thierry& Malines, Caroline& Le Parc, Jean-Marie& Côté, Jean-François. Eosinophilic Fasciitis : A Rare Skin Sclerosis. Pathology Research International. 2010. Vol. 2011, no. 2011, pp.1-4.
https://search.emarefa.net/detail/BIM-492951
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-492951
