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Erschienen in: American Journal of Clinical Dermatology 1/2010

01.06.2010 | Clinical Case

A Case of Dystrophic Epidermolysis Bullosa Improved with Etanercept for Concomitant Psoriatic Arthritis

verfasst von: Dr Emanuela Gubinelli, Corrado Angelo, Valeria Pacifico

Erschienen in: American Journal of Clinical Dermatology | Sonderheft 1/2010

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Abstract

Epidermolysis bullosa is a group of inherited, chronic, non-inflammatory skin disorders, and dystrophic epidermolysis bullosa (DEB) is one of the most severe variants. The role of tumour necrosis factor alpha (TNFα) has not been reported in the pathogenesis of DEB. A DEB case is reported that appears to have responded well to the TNFα inhibitor etanercept given for the treatment of concomitant psoriatic arthritis. A progressive improvement in DEB was apparent over the first 3 months of treatment and persistent good control of DEB was noted over 3 years of therapy. A correlation between DEB improvement and etanercept has not been made, but the case may provide insight into the causal mechanisms of DEB.
Literatur
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Zurück zum Zitat Chopra V, Tyring SK, Johnson L, et al. Patients with severe forms of inherited epidermolysis bullosa exhibit decreased lymphokine and monokine production. J Clin Immunol 1990; 10: 321–9PubMedCrossRef Chopra V, Tyring SK, Johnson L, et al. Patients with severe forms of inherited epidermolysis bullosa exhibit decreased lymphokine and monokine production. J Clin Immunol 1990; 10: 321–9PubMedCrossRef
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Metadaten
Titel
A Case of Dystrophic Epidermolysis Bullosa Improved with Etanercept for Concomitant Psoriatic Arthritis
verfasst von
Dr Emanuela Gubinelli
Corrado Angelo
Valeria Pacifico
Publikationsdatum
01.06.2010
Verlag
Springer International Publishing
Erschienen in
American Journal of Clinical Dermatology / Ausgabe Sonderheft 1/2010
Print ISSN: 1175-0561
Elektronische ISSN: 1179-1888
DOI
https://doi.org/10.2165/1153427-S0-000000000-00000

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