Psammomatoid juvenile ossifying fibroma of mandible in a 6-year-old child.

B S Manjunatha, Sharad Purohit, Sheetal Kiran, V Naga Mahita
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引用次数: 2

Abstract

Juvenile ossifying fibroma (JOF) is a rare fibro-osseous lesion of the jaw occurs at the early age of onset frequently under 15 years with a propensity to recur. It appears as a unilobulated/multilobulated lesion at an early stage followed by radiopaque appearance surrounded by radiolucent rimming at advanced stages. The psammomatous type of JOF (PsJOF) principally involves the bones of the orbit and paranasal sinuses. However in some cases, maxilla or rarely the mandible may be pretentious. Here, we report a challenging case of PsJOF in a 6-year-old child with a complaint of swelling imitating a cystic lesion in left back region of the lower jaw for 2 months. The authors propose that a careful examination and correlations of clinical, radiological, and histopathological features are essential to arrive at correct diagnosis and play a vital role in management of such patients.

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6岁儿童下颌骨类沙砾瘤骨化纤维瘤。
青少年骨化纤维瘤(JOF)是一种罕见的颌骨纤维骨性病变,发生在发病早期,通常在15岁以下,有复发的倾向。早期表现为单叶状/多叶状病变,晚期表现为不透光,周围呈透光边缘。沙漏型JOF (PsJOF)主要累及眶骨和鼻窦。然而,在某些情况下,上颌或很少的下颌骨可能矫情。在这里,我们报告了一个具有挑战性的PsJOF病例,一名6岁儿童,主诉在下颌左后区域出现类似囊性病变的肿胀2个月。作者建议,仔细检查和临床,放射学和组织病理学特征的相关性是必不可少的,以达到正确的诊断,并在这类患者的管理中发挥重要作用。
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