Rhabdomyosarcoma in the Oral Cavity of A Pediatric Patient: A Rare Case

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dc.contributor.authorŞimşek, Betül
dc.contributor.authorDoğan, Esin
dc.contributor.authorKuzuluk, Didar Gürsoy
dc.contributor.authorCemaloğlu, Mustafa
dc.date.accessioned2024-09-19T16:23:26Z
dc.date.available2024-09-19T16:23:26Z
dc.date.issued2023
dc.departmentHatay Mustafa Kemal Üniversitesien_US
dc.description.abstractDear Editor, Rhabdomyosarcoma (RMS) is a rare, aggressive, and malignant neoplasm with rapid growth composed of primitive mesenchymal cells that exhibit skeletal muscle differentiation and mainly affects children and adolescents (60%) [1]. RMS is the most common soft tissue sarcoma with a rate of 50-60% in pediatric patients and ranks third among pediatric extracranial solid tumors, following Wilms tumor and neuroblastoma at a rate of 4-5% [2]. Head and neck localizations constitute 35–40% of cases, with oral lesions being extremely rare [3].en_US
dc.identifier.doi10.26650/jchild.2023.1324273
dc.identifier.endpage400en_US
dc.identifier.issn1302-9940
dc.identifier.issn1308-8491
dc.identifier.issue4en_US
dc.identifier.startpage399en_US
dc.identifier.trdizinid1261656en_US
dc.identifier.urihttps://doi.org/10.26650/jchild.2023.1324273
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/1261656
dc.identifier.urihttps://hdl.handle.net/20.500.12483/15853
dc.identifier.volume23en_US
dc.indekslendigikaynakTR-Dizinen_US
dc.language.isoenen_US
dc.relation.ispartofÇocuk Dergisien_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleRhabdomyosarcoma in the Oral Cavity of A Pediatric Patient: A Rare Caseen_US
dc.typeLetteren_US

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