Abstract | OBJECTIVE: EF is a rare fibrosing disorder that may involve skin and internal organs. Current therapies include moderate- to high-dose glucocorticoids with or without use of immunosuppressives. METHODS: We report three cases of steroid-resistant EF in clinical practice who were treated with 3 mg/kg every 8 weeks infliximab therapy. RESULTS: All patients noticed an improvement in their symptoms, joint contractures and skin thickening within 8 weeks of starting infliximab therapy, ultimately leading to a drug-free remission (range 1-3 years). CONCLUSION: Based on this and other reported cases, infliximab may be beneficial in patients with steroid-resistant EF.
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Authors | Dinesh Khanna, Harsh Agrawal, Philip J Clements |
Journal | Rheumatology (Oxford, England)
(Rheumatology (Oxford))
Vol. 49
Issue 6
Pg. 1184-8
(Jun 2010)
ISSN: 1462-0332 [Electronic] England |
PMID | 20308119
(Publication Type: Case Reports, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anti-Inflammatory Agents
- Antibodies, Monoclonal
- Immunosuppressive Agents
- Steroids
- Infliximab
- Prednisone
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Topics |
- Anti-Inflammatory Agents
(therapeutic use)
- Antibodies, Monoclonal
(therapeutic use)
- Drug Therapy, Combination
- Eosinophilia
(drug therapy, physiopathology)
- Fasciitis
(drug therapy, physiopathology)
- Female
- Humans
- Immunosuppressive Agents
(therapeutic use)
- Infliximab
- Middle Aged
- Prednisone
(therapeutic use)
- Steroids
(therapeutic use)
- Treatment Outcome
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