Scleromyxedema: Treatment with interferon alfa - 07/09/11
Abstract |
Scleromyxedema is a variant of papular mucinosis characterized by fibroblast proliferation and mucin deposition in the dermis. Historically, it has been very difficult to treat and can cause significant morbidity and mortality with systemic involvement. We describe a case of a woman with scleromyxedema and systemic manifestations treated with interferon alfa. Her skin responded very well to therapy within 3 months; however, her systemic manifestations showed little change. We conclude that interferon alfa may be a useful therapy for patients with scleromyxedema, particularly if the disease process is limited to the skin. (J Am Acad Dermatol 1999;40:303-7.)
Le texte complet de cet article est disponible en PDF.Plan
This supplement is made possible through an educational grant from Ortho Dermatological to the American Academy of Dermatology. |
|
Reprint requests: Jaime A. Tschen, MD, 1919 LaBranch, Dermatopathology, Houston, TX 77002. |
|
0190-9622/99/$8.00 + 0 16/4/94736 |
Vol 40 - N° 2S
P. 303-307 - février 1999 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
L’accès au texte intégral de cet article nécessite un abonnement.
Déjà abonné à cette revue ?