Shetty Sujeeth K, Kasrija Rishabh, Choudhary Adarsh, Hariani Amey, Kale Revati M
Department of Oral and Maxillofacial Surgery, Jagadguru Sri Shivarathreeshwara (JSS) Dental College and Hospital, Mysuru, IND.
Cureus. 2025 Feb 14;17(2):e79026. doi: 10.7759/cureus.79026. eCollection 2025 Feb.
Juvenile ossifying fibroma (JOF) is a rare, benign, yet locally aggressive fibro-osseous lesion that primarily affects children and adolescents. This case report describes a 10-year-old female patient presenting with a three-month history of progressive swelling on the right lower third of her face, accompanied by trismus. Clinical examination revealed a firm, non-tender swelling extending from the right corner of the mouth to the angle of the mandible, with buccal cortical expansion and vestibular tenderness near the mandibular right second molar. Radiographic imaging demonstrated ill-defined mixed radiolucent lesions extending to the condylar region of the right mandible, prompting a provisional diagnosis of a fibro-osseous lesion, specifically ossifying fibroma. The histopathological evaluation confirmed the psammomatoid variant of JOF, a rare and aggressive subtype that typically occurs in the sinonasal region, making its mandibular presentation unusual. Given the aggressive nature of this variant, surgical resection was performed to minimize recurrence risk. The defect was reconstructed using a costochondral graft, a preferred method due to its adaptability, biocompatibility, and growth potential, particularly in pediatric patients. Costochondral grafts have been historically favored in maxillofacial reconstruction for their ability to mimic native bone structure and support functional restoration. Costochondral grafts have success in treating mandibular defects, especially in growing individuals, as they allow for continued growth and integration with surrounding tissues. This case highlights the importance of early diagnosis, aggressive surgical management, and effective reconstruction in managing rare and aggressive variants of JOF, ensuring both functional and aesthetic outcomes.
青少年骨化性纤维瘤(JOF)是一种罕见的、良性但具有局部侵袭性的纤维骨性病变,主要影响儿童和青少年。本病例报告描述了一名10岁女性患者,其右下脸三分之一处有进行性肿胀3个月病史,并伴有牙关紧闭。临床检查发现,一个质地坚硬、无压痛的肿胀区从右口角延伸至下颌角,颊侧皮质扩张,右下第二磨牙附近前庭压痛。影像学检查显示边界不清的混合性透光性病变延伸至右下颌骨髁突区,初步诊断为纤维骨性病变,具体为骨化性纤维瘤。组织病理学评估证实为JOF的砂粒体样变体,这是一种罕见且侵袭性的亚型,通常发生在鼻窦区域,其在下颌骨的表现并不常见。鉴于该变体的侵袭性,进行了手术切除以降低复发风险。缺损采用肋软骨移植进行重建,这是一种首选方法,因为它具有适应性、生物相容性和生长潜力,尤其适用于儿科患者。肋软骨移植因其能够模拟天然骨结构并支持功能恢复,在历史上一直受到颌面重建的青睐。肋软骨移植在治疗下颌骨缺损方面取得了成功,特别是在生长中的个体中,因为它们允许持续生长并与周围组织融合。本病例强调了早期诊断、积极手术管理和有效重建在处理JOF罕见且侵袭性变体中的重要性,以确保功能和美学效果。