Abstract |
Pityriasis rubra pilaris (PRP) or Devergie's disease is a chronic and rare papulosquamous disorder of unknown etiology characterized by reddish orange scaly plaques, palmoplantar keratoderma, and keratotic follicular papules. The present authors report a case of a 30-year-old woman with clinical and histologic signs of PRP (type I adult onset, Griffith's classification). After a few unsuccessful treatments, the present authors chose to start etanercept. Total clearing of the lesions was achieved 5 months after starting the drug. Etanercept is a TNF-α inhibitor, and today it is largely used in the treatment of several dermatological diseases through blockage of the inflammatory cytokine. The true mechanism of action in PRP remains to be explained; however, the favorable results in our case raise new questions about TNF-α's role in PRP and suggest a therapeutic alternative for resistant cases to classic treatments. To date, there are only three case reports of PRP treated with etanercept in the literature.
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Authors | Rita Guedes, Luiz Leite |
Journal | Dermatologic therapy
(Dermatol Ther)
2011 Mar-Apr
Vol. 24
Issue 2
Pg. 285-6
ISSN: 1529-8019 [Electronic] United States |
PMID | 21410618
(Publication Type: Case Reports, Journal Article)
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Copyright | © 2011 Wiley Periodicals, Inc. |
Chemical References |
- Dermatologic Agents
- Immunoglobulin G
- Receptors, Tumor Necrosis Factor
- Etanercept
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Topics |
- Adult
- Biopsy
- Dermatologic Agents
(therapeutic use)
- Etanercept
- Female
- Humans
- Immunoglobulin G
(therapeutic use)
- Pityriasis Rubra Pilaris
(diagnosis, drug therapy)
- Receptors, Tumor Necrosis Factor
(therapeutic use)
- Skin
(drug effects, pathology)
- Time Factors
- Treatment Outcome
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