Juvenile ossifying fibroma of the mandible: a case report.

IF 1 Q3 DENTISTRY, ORAL SURGERY & MEDICINE
eJournal of Oral Maxillofacial Research Pub Date : 2010-07-01 eCollection Date: 2010-01-01 DOI:10.5037/jomr.2010.1205
Bahar Keles, Mutlu Duran, Yavuz Uyar, Ahmet Azimov, Abdullah Demirkan, Haci Hasan Esen
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Abstract

Background: Fibro-osseous lesions of the jaws, including juvenile ossifying fibroma, pose diagnostic and therapeutic difficulties due to their clinical, radiological and histological variability. The aim of this study was to report the outcome of a 9 years old girl with diagnosed juvenile ossifying fibroma treatment.

Methods: A 9 years old girl presented with a 6 x 8 cm sized hard fixed tumour on right ramus and corpus of the mandible. On the radiological examination tumour showed an irregular but well bordered, unilocular and expansive lesion on the right corpus and ramus of the mandible. There was no teeth displacement or teeth root resorbtion. Microscopically, the tumour had trabeculae, fibrillary osteoid and woven bone. After the clinical, radiological (panoramic radiography, computed tomography and magnetic resonance imaging) and histologic analysis it was diagnosed juvenile ossifying fibroma. In the history of the patient there has been an acute lymphocytic leukaemia in the remission for 3 years.

Results: Because of large size of mandibular tumour, resultant expansion and destruction of mandibular cortex, the patient underwent right hemimandibulectomy using transmandibular approach. There was no recurrence or complications for two years follow-up.

Conclusions: Although juvenile ossifying fibroma is an uncommon clinical entity, its aggressive local behaviour and high recurrence rate means that it is important to make an early diagnosis, apply the appropriate treatment and, especially, follow-up the patient over the long-term.

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下颌骨幼年骨化纤维瘤:病例报告。
背景:包括幼年骨化性纤维瘤在内的颌骨纤维骨病变因其临床、放射学和组织学上的多变性而给诊断和治疗带来困难。本研究旨在报告一名 9 岁女孩确诊为幼年骨化性纤维瘤的治疗结果:方法:一名 9 岁女孩因右侧下颌骨横梁和牙冠上长有一个 6 x 8 厘米大小的硬性固定肿瘤而就诊。放射学检查显示,肿瘤位于下颌骨右侧齿冠和颌骨上,呈不规则但边界清楚的单发膨胀性病变。牙齿没有移位,牙根也没有吸收。显微镜下,肿瘤内有骨小梁、纤维状骨质和编织骨。经过临床、放射学(全景放射摄影、计算机断层扫描和磁共振成像)和组织学分析,诊断为幼年骨化性纤维瘤。患者曾患急性淋巴细胞白血病,病情缓解了 3 年:由于下颌骨肿瘤体积较大,导致下颌骨皮质扩张和破坏,患者接受了经下颌途径的右半下颌骨切除术。随访两年,患者未出现复发或并发症:虽然幼年骨化性纤维瘤在临床上并不常见,但其侵袭性局部表现和高复发率意味着早期诊断、适当治疗,尤其是长期随访非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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