Pace Clarence, Crosher Richard, Holt Donald, Pace Audrey
Oral and Maxillofacial Surgery, Rotherham Hospitals NHS Trust, Rotherham, UK.
J Oral Sci. 2010 Jun;52(2):329-32. doi: 10.2334/josnusd.52.329.
Juvenile ossifying fibroma (JOF) is an uncommon fibro-osseous lesion occurring in the facial bones. It has been recognised as a separate histopathological entity among the fibro-osseous group of lesions. Fibro-osseous lesions of the craniofacial bones are difficult to classify and treat however a common factor to all is the conversion of the bone to benign fibrous tissue with a varying degree of mineralised tissue. This case describes a 15 year old patient with a juvenile aggressive ossifying fibroma (JAOF) and an estimate of the rate of growth of such a rare lesion.
青少年骨化性纤维瘤(JOF)是一种发生于面骨的罕见纤维骨性病变。它已被公认为纤维骨性病变组中的一个独立组织病理学实体。颅面骨的纤维骨性病变难以分类和治疗,然而所有这些病变的一个共同因素是骨转化为良性纤维组织,并伴有不同程度的矿化组织。本病例描述了一名患有青少年侵袭性骨化性纤维瘤(JAOF)的15岁患者,并对这种罕见病变的生长速度进行了评估。