AB0979 Eosinophilic fascitis: clinical experience in a series of 21 patients. (15th June 2017)
- Record Type:
- Journal Article
- Title:
- AB0979 Eosinophilic fascitis: clinical experience in a series of 21 patients. (15th June 2017)
- Main Title:
- AB0979 Eosinophilic fascitis: clinical experience in a series of 21 patients
- Authors:
- Quevedo, JC
Lopez, R
Garcia-Bustuinduy, M
Rodriguez-Lozano, C
Rodriguez-Lozano, B
Bustabad, S
Trujillo, E - Abstract:
- Abstract : Background: The Eosinophilic fascitis (EF) is a uncommon sclerodermiforme síndrome with unknown etiology and poorly understood pathogenesis and natural evolution. The published series are short, with a total of 280 cases described in the literature from 1974. There is neither clinical tests nor consensus on the EF treatment. Objectives: To describe a series of 21 patients with EF. Methods: Multicentric, retrospective Case Series Study. We reviewed 21 patients diagnosed of EF (cutaneous induration+consistent biopsy) between January 1998 to January 2015. A total of 13 males and 8 females. Results: The mean age at diagnosis was 41 years 8range between 28 and 66). Trigger factor was suspected in 8 patients (intense exercise in 7). The zones of cutaneous affectation were fundamentally the upper and low extremities. The hyperesonophilia was present in 100% of the patients. The average of the % more high of hyperesosinophilia was 21.2% (range 4–45.4%). 11 patients presented artralgias and 5 patients presented arthritis (4 polyarticular/1 oligoarticular). The MRI was used for diagnosis and/or follow-up in 8 patients, especially in the diagnosed ones in the last 5 years. The average initial dose of prednisone was 40 mg/día, the average maximum dose of prednisone was 40 mg/dia and the mean steroid treatment duration was 22 months (range 9–47 months). Other immunomodulatory agents were: methotrexate 11, hydroxychloroquine 2, azatioprina 2 and D penicillamine 1. 5 years afterAbstract : Background: The Eosinophilic fascitis (EF) is a uncommon sclerodermiforme síndrome with unknown etiology and poorly understood pathogenesis and natural evolution. The published series are short, with a total of 280 cases described in the literature from 1974. There is neither clinical tests nor consensus on the EF treatment. Objectives: To describe a series of 21 patients with EF. Methods: Multicentric, retrospective Case Series Study. We reviewed 21 patients diagnosed of EF (cutaneous induration+consistent biopsy) between January 1998 to January 2015. A total of 13 males and 8 females. Results: The mean age at diagnosis was 41 years 8range between 28 and 66). Trigger factor was suspected in 8 patients (intense exercise in 7). The zones of cutaneous affectation were fundamentally the upper and low extremities. The hyperesonophilia was present in 100% of the patients. The average of the % more high of hyperesosinophilia was 21.2% (range 4–45.4%). 11 patients presented artralgias and 5 patients presented arthritis (4 polyarticular/1 oligoarticular). The MRI was used for diagnosis and/or follow-up in 8 patients, especially in the diagnosed ones in the last 5 years. The average initial dose of prednisone was 40 mg/día, the average maximum dose of prednisone was 40 mg/dia and the mean steroid treatment duration was 22 months (range 9–47 months). Other immunomodulatory agents were: methotrexate 11, hydroxychloroquine 2, azatioprina 2 and D penicillamine 1. 5 years after follow-up, the evolution was the complete resolution in 13 patients and the partial improvement in 6. Conclusions: In our series, the EF prevails in males, in the decade of the 40 and in the majority one did not find trigger factor. There was presence of arthritis in a significant percentage of patients. In the last years the use of the RMN has been added to the diagnosis and to the follow-up. Though there are no clinical tests that support it the use of the metotrexato has been generalized as adjuvant treatment to the steroids. Disclosure of Interest: None declared … (more)
- Is Part Of:
- Annals of the rheumatic diseases. Volume 76(2017)Supplement 2
- Journal:
- Annals of the rheumatic diseases
- Issue:
- Volume 76(2017)Supplement 2
- Issue Display:
- Volume 76, Issue 2 (2017)
- Year:
- 2017
- Volume:
- 76
- Issue:
- 2
- Issue Sort Value:
- 2017-0076-0002-0000
- Page Start:
- 1397
- Page End:
- 1397
- Publication Date:
- 2017-06-15
- Subjects:
- Rheumatism -- Periodicals
616.723005 - Journal URLs:
- http://ard.bmjjournals.com/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=149&action=archive ↗
http://www.bmj.com/archive ↗
http://gateway.ovid.com/server3/ovidweb.cgi?T=JS&MODE=ovid&D=ovft&PAGE=titles&SEARCH=annals+of+the+rheumatic+diseases.tj&NEWS=N ↗ - DOI:
- 10.1136/annrheumdis-2017-eular.6444 ↗
- Languages:
- English
- ISSNs:
- 0003-4967
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - BLDSS-3PM
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