Rhabdomyosarcoma of the oral cavity in children aged zero to two years: a scoping review.

Mariana Mota NunesAdriana Aparecida Silva da CostaThalita Soares TavaresMaria Cássia Ferreira AguiarCarolina Castro MartinsPatrícia Carlos Caldeira

Published in: Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology (2023)

Oral rhabdomyosarcoma is rare in children aged zero to two 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.

Keyphrases

end stage renal disease
ejection fraction
newly diagnosed
chronic kidney disease
peritoneal dialysis
prognostic factors
mental health
physical activity
patient reported outcomes