Rhabdomyosarcoma of the oral cavity in children aged 0-2 years: a scoping review

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dc.creatorMariana Mota Nunes
dc.creatorAdriana Aparecida Silva da Costa
dc.creatorThalita Soares Tavares
dc.creatorMaria Cássia Ferreira de Aguiar
dc.creatorCarolina Castro Martins
dc.creatorPatrícia Carlos Caldeira
dc.date.accessioned2024-09-10T22:21:26Z
dc.date.accessioned2025-09-08T23:29:03Z
dc.date.available2024-09-10T22:21:26Z
dc.date.issued2023
dc.description.sponsorshipCAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
dc.format.mimetypepdf
dc.identifier.doihttps://doi.org/10.1111/jop.13411
dc.identifier.issn1600-0714
dc.identifier.urihttps://hdl.handle.net/1843/76322
dc.languagepor
dc.publisherUniversidade Federal de Minas Gerais
dc.relation.ispartofJournal of Oral Pathology & Medicine
dc.rightsAcesso Restrito
dc.subjectChild
dc.subjectInfant
dc.subjectMouth
dc.subjectRhabdomyosarcoma
dc.subjectSarcoma
dc.subjectClinical study
dc.subjectDemography
dc.subjectTongue
dc.subjectLip
dc.subjectSurgery, oral
dc.subjectPrognosis
dc.subjectNeoplasms
dc.subject.otherChildren
dc.titleRhabdomyosarcoma of the oral cavity in children aged 0-2 years: a scoping review
dc.typeArtigo de periódico
local.citation.epage475
local.citation.issue6 Journal of Oral Pathology & Medicine (online)
local.citation.spage468
local.citation.volume52
local.description.resumoBackground: The aim of this study was to collect, synthesize, and analyze the clinic-demographic data of rhabdomyosarcoma affecting the oral cavity of young children. Methods: The clinical question was "What are the clinical characteristics of oral rhabdomyosarcoma in children aged zero to two years?" Two independent reviewers selected the studies, extracted data, and assessed the methodological quality through the Joanna Briggs Institute Checklist. Descriptive statistics were performed in SPSS. (protocol: osf.io/b9hvy). Results: Thirty case reports with 41 patients were included (22 males; mean age at diagnosis: 15 months). All studies had some methodological limitations, mainly due to the lack of clarity for a final judgment. More than 70% of the cases affected the tongue or lips. Tumors had a fast growth (mean 2.5 months), usually with red coloration, and variable shape and consistency. Embryonal (63.41%) and alveolar (29.27%) were the most common histological subtypes. Treatment was quite variable but usually included surgery. Most patients (53.66%) were alive without disease at follow-up. Conclusion: Oral rhabdomyosarcoma is rare in children aged 0-2 years without a marked gender predilection. The tumor presents as a fast and infiltrative growth leading to local and/or systemic symptoms, and a favorable prognosis for most patients.
local.publisher.countryBrasil
local.publisher.departmentFAO - DEPARTAMENTO DE CLÍNICA
local.publisher.departmentFAO - DEPARTAMENTO DE ODONTOPEDIATRIA E ORTODONTIA
local.publisher.initialsUFMG
local.url.externahttps://onlinelibrary.wiley.com/doi/10.1111/jop.13411

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