Abuzinada Sondos, Alyamani A
Faculty of Dentistry, King Abdulaziz University, Jeddah, Saudi Arabia ; P.O.Box 419, Jeddah, Saudi Arabia.
J Maxillofac Oral Surg. 2010 Mar;9(1):91-5. doi: 10.1007/s12663-010-0027-6. Epub 2010 Jun 4.
We present three cases with juvenile ossifying fibroma. Two occurring in the maxilla, and one in the mandible. All three cases presented with a major swelling in the face. After clinical and radiological evaluation the lesions were surgically excised and sent for histopathological evaluation. Two histological types of juvenile ossifying fibroma were found, the psammatous type in two cases and the trabecular pattern in one case. Although juvenile ossifying fibroma is an uncommon clinical entity, its aggressive local behaviour and high recurrence rate mean that it is important to make an early diagnosis. It is also important to apply the appropriate treatment and to follow-up the patient closely over the long term. This report describes the diagnosis and treatment of juvenile ossifying fibroma in the maxilla and the mandible. It also emphasizes the importance of considering the less aggressive options as a first line of treatment before choosing the aggressive approach when dealing with children.
我们报告三例青少年骨化性纤维瘤病例。两例发生在上颌骨,一例发生在下颌骨。所有三例患者均表现为面部明显肿胀。经临床和影像学评估后,对病变进行手术切除并送去做组织病理学评估。发现了两种青少年骨化性纤维瘤的组织学类型,两例为沙砾体型,一例为小梁型。尽管青少年骨化性纤维瘤是一种不常见的临床病症,但其侵袭性的局部行为和高复发率意味着早期诊断很重要。采用适当的治疗方法并对患者进行长期密切随访也很重要。本报告描述了上颌骨和下颌骨青少年骨化性纤维瘤的诊断和治疗。它还强调了在处理儿童患者时,在选择激进治疗方法之前,将侵袭性较小的治疗方案作为一线治疗方案的重要性。