Gorlin-Goltz syndrome

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dc.authorid0000-0001-9947-7690
dc.authorid0000-0001-7091-5650
dc.authorid0000-0003-0819-4578
dc.contributor.authorŞereflican, Betül
dc.contributor.authorTuman, Bengü
dc.contributor.authorŞereflican, Murat
dc.contributor.authorHalıcıoğlu, Sıddıka
dc.contributor.authorÖzyalvaçlı, Gülzade
dc.contributor.authorBayrak, Seval
dc.date.accessioned2021-06-23T19:45:28Z
dc.date.available2021-06-23T19:45:28Z
dc.date.issued2017
dc.departmentBAİBÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.description.abstractGorlin-Goltz syndrome is a rare multisystemic disease inherited in an autosomal dominant pattern. It is characterized by numerous basal cell carcinoma of the skin, jaw cysts, and skeletal anomalies such as frontal bossing, vertebral anomalies, palmoplantar pits, and falx cerebri calcification. There is a tendency to tumors including medullablastoma, fibroma, rabdomyoma, leiomyosarcoma etc.. The diagnosis is based on major and minor clinical and radiologic criteria. Early diagnosis and treatment are of utmost importance in reducing the severity of long-term sequelae of this syndrome. In this article, we present a 15-year-old boy who was admitted to our clinic with brown-black papules and plaques on his scalp and was thought to have Gorlin-Goltz syndrome. He had a history of medulloblastoma that was treated with surgical resection followed by cranial radiotherapy and unilateral retinoblastoma. We present this case, because association of Gorlin-Goltz syndrome and retinoblastoma has not been described previously in the literature and we aimed to draw attention to radiation-induced basal cell carcinomas.en_US
dc.identifier.doi10.5152/TurkPediatriArs.2017.2992
dc.identifier.endpage177en_US
dc.identifier.issn1306-0015
dc.identifier.issn1308-6278
dc.identifier.issue3en_US
dc.identifier.pmid29062253en_US
dc.identifier.scopus2-s2.0-85031110938en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage173en_US
dc.identifier.urihttps://doi.org/10.5152/TurkPediatriArs.2017.2992
dc.identifier.urihttps://hdl.handle.net/20.500.12491/9158
dc.identifier.volume52en_US
dc.identifier.wosWOS:000413141200011en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.institutionauthorŞereflican, Betül
dc.institutionauthorTuman, Bengü
dc.institutionauthorŞereflican, Murat
dc.institutionauthorHalıcıoğlu, Sıddıka
dc.institutionauthorÖzyalvaçlı, Gülzade
dc.institutionauthorBayrak, Seval
dc.language.isoenen_US
dc.publisherAvesen_US
dc.relation.ispartofTurk Pediatri Arsivi-Turkish Archives Of Pediatricsen_US
dc.relation.publicationcategoryOlgu Sunumu - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBasal Cell Carcinomaen_US
dc.subjectGorlin-Goltz Syndromeen_US
dc.subjectMedulloblastomaen_US
dc.subjectRetinoblastomaen_US
dc.titleGorlin-Goltz syndromeen_US
dc.typeCase Reporten_US

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