Silva Carolina Amália Barcellos, Silva Alessandra Dutra, Soares José Antônio de Carvalho, Furuse Cristiane, de Araújo Ney Soares, de Araújo Vera Cavalcanti
São Leopoldo Mandic Institute and Research Center, Campinas, São Paulo, Brazil.
Pediatr Dent. 2011 Sep-Oct;33(5):388-91.
Juvenile ossifying fibroma is an uncommon, benign, bone-forming neoplasm that is distinguished from other fibro-osseous lesions primarily by its age of onset, clinical presentation, and potential behavior. It mainly occurs in juveniles and has a slight male predilection and more aggressive behavior than a common ossifying fibroma. There are 2 distinct histopathological variants of this lesion: (1) psammomatoid pattern and (2) trabecular pattern. An aneurysmal bone cyst may occur in association with other bone lesions, such as fibrous dysplasia, ossifying fibroma, and giant cell lesion. The clinical management and prognosis of juvenile ossifying fibroma is somewhat uncertain, and this tumor has high rates of recurrence. Such behavior may be related to younger patient age and the concurrent development of aneurysmal bone cyst. The purpose of this paper was to report a case of trabecular juvenile ossifying fibroma in a 9-year-old girl associated with an aneurysmal bone cyst, presenting an aggressive behavior, and causing significant facial asymmetry.
青少年骨化性纤维瘤是一种罕见的良性成骨性肿瘤,主要通过发病年龄、临床表现和潜在行为与其他纤维-骨病变相鉴别。它主要发生于青少年,男性略多见,与普通骨化性纤维瘤相比具有更具侵袭性的行为。该病变有两种不同的组织病理学变体:(1)砂粒体样型和(2)小梁型。动脉瘤样骨囊肿可与其他骨病变相关联,如骨纤维结构不良、骨化性纤维瘤和巨细胞病变。青少年骨化性纤维瘤的临床处理和预后尚不确定,且该肿瘤复发率高。这种行为可能与患者年龄较小以及动脉瘤样骨囊肿的并发有关。本文的目的是报告一例9岁女孩的小梁型青少年骨化性纤维瘤,伴有动脉瘤样骨囊肿,表现出侵袭性行为,并导致明显的面部不对称。