Fibroma ossificante juvenil psamomatoide: relato de caso.

Abstract

The present study aims to conduct a literature review on juvenile psammomatoid ossifying fibroma, a rare condition and to report the case of a patient diagnosed with the pathology, whose surgical treatment resulted in adequate control, with no signs of recurrence up to the present time. This is a disease with few cases described in the literature, which justifies the importance of an in-depth study. The methodology involved the analysis of the patient's electronic medical record and a review of scientific articles published in the last five years, obtained from the PubMed and SciELO databases. The inclusion criterion was the selection of articles published in the last five years, and the exclusion criterion was older studies. The study aims to provide a better understanding of the diagnostic methods and clinical behavior of this condition, which may present diagnostic challenges due to its rarity. The conclusion points out that juvenile psammomatoid ossifying fibroma is a pathology for which early detection is crucial for a favorable prognosis. The described case had a positive outcome, due to the rapid diagnosis and effective surgical intervention, which prevented more severe complications.