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Title: Severe pyoderma gangrenosum unresponsive to etanercept and adalimumab
Author(s): Kleinpenning, M.M. (298210959)
Langewouters, A.M.G. (298209071)
Kerkhof, P.C.M. van de (069296987)
Greebe, R.J.
Publication year: 2011
Document type: Article / Letter to editor
Journal: Journal of Dermatological Treatment
ISSN: 0954-6634
Volume: vol. 22
Issue: iss. 5
Start page: p. 261
End page: p. 265
Annotation: Kleinpenning, Marloes M Langewouters, Annechien M G Van De Kerkhof, Peter C M Greebe, Rens J England J Dermatolog Treat. 2011 Oct;22(5):261-5. doi: 10.3109/09546631003797106. Epub 2010 Aug 1.
Abstract: BACKGROUND: A 74-year-old female with severe and therapy-resistant pyoderma gangrenosum (PG) was treated for more than 40 years with topical antibacterial ointments, topical and systemic corticosteroids, dapsone and azathioprine. Generally, immunosuppression is the mainstay of treatment of PG, but in our patient cyclosporine had to be discontinued because of significant serious side effects. An attempt was made to decrease the amount of steroids, but tapering of the prednisone dose resulted in relapses of PG. OBSERVATION: Off-label use of etanercept resulted in a temporary limited clinical improvement. After 6 months, initial clinical improvement reduced and adalimumab was started. Unfortunately, after 6 months of adalimumab no clinical improvement was seen. Therefore, systemic corticosteroids had to be continued with very good clinical results. CONCLUSION: In concordance with previous results of several other studies, reviews and case reports, we presume that possibly both etanercept and adalimumab could be excellent therapeutic alternatives in the treatment of PG. Unfortunately, the effectiveness of both etanercept and adalimumab were very limited in our case. Literature research revealed no other successful studies on the off-label use of other immunomodulators as an alternative treatment option for PG. However, infliximab or ustekinumab could be alternative treatment options.
Subject: N4i 1: Pathogenesis and modulation of inflammation
N4i 1: Pathogenesis and modulation of inflammation NCEBP 2: Evaluation of complex medical interventions
Organization: Dermatology
UMCN Extern
Appears in Collections:Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/98345

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