Juvenille psammomatoid ossifying fibroma Case report
Alexandros VALASIDIS, Aris NTOMOUCHTSIS, Antonis TSEKOS, Giorgos BALLIS, Persephone XIROU, Konstantinos VAHTSEVANOS, Doxa MAGGOUDI
Department of Oral and Maxillofacial Surgery and Department of Pathology. “Theagenio” Anti-Cancer Hospital, Thessaloniki, Greece.
Hellenic Archives of Oral & Maxillofacial Surgery (2012) 2, 107-114
SUMMARY: Ossifying fibroma (OS) represents a slowgrowing, benign neoplasm that belongs to the greater group of fibro-osseous lesions. Based on its histological features, ossifying fibroma is divided into: a) juvenile trabecular OS and b) juvenile psammomatoid OS which affects mainly the paranasal sinuses of children and teenagers aging from 5 to 15 years. A rare case of juvenile psammomatoid ossifying fibroma in a 30 year old male patient located in the left mandibular ramus is presented. Treatment plan included radical surgical excision of the lesion and restoration with autologous osteochondral graft from the 6th rib of the ipsilateral side.
KEY WORDS: juvenile psammomatoid ossifying fibroma, cone-beam computed tomography, costochondral autologous graft, bone scintigraphy with 99Tc
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