Malathi N, Radhika T, Thamizhchelvan H, Ravindran C, Ramkumar S, Giri Gvv, Gopal Deepika
Departments of Oral and Maxillofacial Pathology, Faculty of Dental Sciences, Sri Ramachandra University and Hospital, Porur, Chennai, Tamil Nadu, India.
J Oral Maxillofac Pathol. 2011 Sep;15(3):326-9. doi: 10.4103/0973-029X.86710.
Juvenile ossifying fibroma is an uncommon, benign, bone-forming neoplasm with aggressive local growth that is distinguished from other fibro-osseous lesions primarily by its age of onset, clinical presentation and aggressive behavior. Although a benign entity, juvenile ossifying fibroma is known to be locally aggressive and has a high tendency to recur. Two distinctive microscopic patterns have been described: A trabecular variant and a psammomatoid variant. This latter variant is predominantly a craniofacial lesion and occurs rarely in the jaws. We present herein two cases of psammomatoid juvenile ossifying fibroma involving the jaws. The first case was a mandibular lesion in a 31-year-old female whereas the second case presented with maxillary involvement in a 46-year-old female. In addition, the pathology of the lesion was analyzed with confocal laser scanning microscopy.
青少年骨化性纤维瘤是一种罕见的、良性的、形成骨的肿瘤,具有侵袭性局部生长特点,主要通过发病年龄、临床表现和侵袭性行为与其他纤维-骨病变相鉴别。尽管青少年骨化性纤维瘤是良性病变,但已知其具有局部侵袭性且复发倾向高。已描述了两种独特的微观模式:小梁状变体和砂粒体样变体。后一种变体主要是颅面部病变,很少发生于颌骨。我们在此报告两例累及颌骨的砂粒体样青少年骨化性纤维瘤病例。第一例是一名31岁女性的下颌病变,而第二例是一名46岁女性的上颌受累。此外,用共聚焦激光扫描显微镜对病变的病理进行了分析。