Purely Cutaneous Rosai-Dorfman disease (CRDD) Co-Existed with Capillary Hemangioma Successfully Treated with Intralesional Corticosteroid
Wanlapa Asawabenjang MD*, Suthep Jerasutus MD**, Pinnaree Kattipathanapong MD*, Patcharin Janjumratsang MD*, Chinmanat Tangjaturonrusamee MD*
Affiliation : * Institute of Dermatology, Department of Medical Services, Ministry of Public Health, Bangkok, Thailand ** Lions Supannahong Clinic, Bangkok, Thailand
Rosai-Dorfman disease (RDD), or sinus histiocytosis with massive lymphadenopathy, is a benign idiopathic proliferative disorder of the histiocyte. Purely Cutaneous Rosai-Dorfman disease (CRDD) is a separated clinical entity without lymph node and organ involvement. The histologic features resemble RDD, but with dermal infiltration. This rare condition is benign and mostly self-limited. The authors report a 66-year-old Thai male patient, diagnosed as purely CRDD, with co-existing capillary hemangioma. In addition, we show that the treatment intralesional corticosteroid can produce the remission of the plaque and tumoral types of this condition.
Keywords : Rosai-dorfman disease, Capillary hemangioma, Intralesional corticosteroid
