Ossifying fibroma (OF) is a benign fibro-osseous lesion. It is characterized by the presence of well-demarcated borders and cell-rich fibrosis and contains varying amounts of calcified tissues such as bone or cementum, or both. OF is classified into cemento-OF, juvenile trabecular OF and juvenile psammomatoid OF (JPOF) [1]. JPOF usually occurs before the age of 15 years, but it can also reportedly occur in adults [2-5]. It has a predilection for the paranasal sinuses and can occur in the maxilla, mandible, orbit, fronto-ethmoid complex, and frontal bone [2-8]. The diagnosis of JPOF is based on characteristic clinical manifestations, histological examination, and radiological characteristics. It is usually asymptomatic but short-term rapid growth of the mass can cause facial asymmetry, and when the maxilla, mandible, or both are affected it can also cause dental symptoms [2,7,8]. Histopathological JPOF exhibits dense cellularity with fibrous stroma and psammoma bodies. Radiological examinations have yielded a large spectrum of findings, including locularity, radiodensity, and cortical bone perforation [2,7]. Complete removal is the recommended treatment for JPOF because of its aggressive and locally invasive characteristics, but conservative local excision such as curettage, enucleation, or partial excision can be attempted depending on the patient's individual condition [2,3,9]. CASE REPORT A 20-year-old man was referred to our clinic by the department of otorhinolaryngology. Ten months prior he had noticed a mass on his right cheek, which was initially tender. Three months thereafter the mass had started increasing in size, and Archives of Craniofacial Surgery