Gürlevik, ZehraAlbayrak, HülyaYanık, Mehmet EminGüvenç, Serdar CenkŞahin, A. Fahri2020-04-302020-04-3020101307671Xhttps://hdl.handle.net/20.500.12684/405Juvenile pityriasis rubra pilaris (PRP) is an uncommon skin disease characterized by follicular keratotic papules, erythemato-squamous plaques and palmoplantar keratoderma. Etyology is unknown. A 8 years-old boy presented with a 15 days history of scaly patches and plaques with follicular papules involving his scalp and face. However he had palmoplantar keratoderma on his hands and feet. Based upon clinical and histopatological findings, he was diagnosed as Juvenile PRP. Acitretin was initiated for therapy. We presented our case because of its rarity. © 2010 Düzce Medical Journal.trinfo:eu-repo/semantics/closedAccessArticle1219193Q4