Juvenil Pityriasis Rubra pilaris: A case report

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dc.contributor.authorGürlevik, Zehra
dc.contributor.authorAlbayrak, Hülya
dc.contributor.authorYanık, Mehmet Emin
dc.contributor.authorGüvenç, Serdar Cenk
dc.contributor.authorŞahin, A. Fahri
dc.date.accessioned2020-04-30T13:32:42Z
dc.date.available2020-04-30T13:32:42Z
dc.date.issued2010
dc.departmentDÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.description.abstractJuvenile 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.en_US
dc.identifier.endpage93en_US
dc.identifier.issn1307671X
dc.identifier.issue1en_US
dc.identifier.scopusqualityQ4en_US
dc.identifier.startpage91en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12684/405
dc.identifier.volume12en_US
dc.indekslendigikaynakScopusen_US
dc.language.isotren_US
dc.relation.ispartofDüzce Tıp Fakültesi Dergisi
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleJuvenil Pityriasis Rubra pilaris: A case reporten_US
dc.title.alternativeJüvenil Pitriyazis Rubra pilaris: Vaka sunumuen_US
dc.typeArticleen_US

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