A Novel Management Strategy of Dowling Degos Disease in Association with Hidradenitissupprative in an Iranian Middle Aged Woman

Abstract

Introduction: Dowling-Degos disease (DDD) is an unusual autosomal dominant inherited genodermatosis. It is clinically characterized by reticular pigmented macules of flexoral sites. Case Presentation: We reported a rare association of DDD and Hidradenitis supprativa in an Iranian middle aged woman. Conclusions: A clinical and histopathologic examination showed specific features of both diseases simultaneously. Additionally, a novel treatment for this worrisome disease was discussed.