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dc.contributor.authorAcer, E.
dc.contributor.authorKaya, Erdoğan H.
dc.contributor.authorTad, M.
dc.contributor.authorSaraçoğlu, N.
dc.date.accessioned2019-11-24T21:01:33Z
dc.date.available2019-11-24T21:01:33Z
dc.date.issued2017
dc.identifier.issn1300-0330
dc.identifier.urihttps://dx.doi.org/10.5336/dermato.2017-56443
dc.identifier.urihttps://hdl.handle.net/20.500.12513/3536
dc.description.abstractPorokeratosis mibelli (PM) is a rare, chronic keratinization disorder that has unknown etiology and may be inherited. PM is considered a premalign lesion, characterized by thin plaques with atrophic center and surrounded by a hyperkeratotic border. PM is more common in men and is usually located in the extremities, but occasionally the involvement of the face and genital area is also seen. Because of the potential for malignant degeneration, treatment and follow-up of PM must be performed. Here, we present a 17-years-old female patient who diagnosed with PM in the face region and performed cryotherapy and PM is discussed in the light of the literature. Copyright © 2017 by Türkiye Klinikleri.en_US
dc.language.isoturen_US
dc.publisherOrtadogÂ?u Reklam Tanitim Yayincilik Turizm Egitim Insaat Sanayi ve Ticaret A.S.en_US
dc.relation.isversionof10.5336/dermato.2017-56443en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCryotherapyen_US
dc.subjectFaceen_US
dc.subjectPorokeratosisen_US
dc.titlePorokeratosis mibelli [Porokeratozis mibelli]en_US
dc.typearticleen_US
dc.relation.journalTurkiye Klinikleri Dermatolojien_US
dc.contributor.departmentKırşehir Ahi Evran Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri, Tıbbi Pataloji ABDen_US
dc.identifier.volume27en_US
dc.identifier.issue3en_US
dc.identifier.startpage125en_US
dc.identifier.endpage127en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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