Adrenocortical tumor: Report of two cases

Basit Öğe Kaydı
dc.authorid0000-0001-5608-5742
dc.authorid0000-0002-1162-5140
dc.contributor.authorÖztürk, Hülya
dc.contributor.authorÖztürk, Hayrettin
dc.contributor.authorDokucu, Ali Ihsan
dc.contributor.authorDuran, Hatun
dc.date.accessioned2021-06-23T18:54:15Z
dc.date.available2021-06-23T18:54:15Z
dc.date.issued2006
dc.departmentBAİBÜ, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümüen_US
dc.description.abstractFunctioning adrenocortical tumor is rare in children. Although most are benign, both benign and malignant lesions may present with virilizing and Cushingoid features. We present two cases of adrenocortical tumor. The symptoms and signs at presentation were virilization. Cushingoid features, precocious puberty and hypertension. Both children underwent resection of the tumors. The presenting symptoms, postoperative course, adjuvant therapy, clinical course are described and the literature is reviewed.en_US
dc.identifier.endpage29en_US
dc.identifier.issn1305-5194
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-33745739427en_US
dc.identifier.scopusqualityQ4en_US
dc.identifier.startpage27en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12491/4337
dc.identifier.urihttps://journalpedsurg.org/index.jsp?mod=tammetin&makaleadi=&makaleurl=CCD_20_1_27_29.pdf&key=53487
dc.identifier.volume20en_US
dc.indekslendigikaynakScopusen_US
dc.institutionauthorÖztürk, Hayrettin
dc.language.isotren_US
dc.relation.ispartofCocuk Cerrahisi Dergisien_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAdrenocortical Tumoren_US
dc.subjectChilden_US
dc.subjectPrecocious Pubertyen_US
dc.titleAdrenocortical tumor: Report of two casesen_US
dc.title.alternativeAdrenokortikal tümör: İki olgu sunumuen_US
dc.typeConference Objecten_US

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