A rare case of bone lesion: Mandible's fibrous dysplasia.

National journal of maxillofacial surgery Pub Date : 2024-09-01 Epub Date: 2024-11-16 DOI:10.4103/njms.njms_35_23
Pietro Fusari, Federico Guerri, Matteo Arcari, Andrea Sardella
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引用次数: 0

Abstract

Fibrous dysplasia is a rare genetic syndrome that affects bone tissue. This pathology replaces the mineralized matrix of the bone affected with connective and fibrous tissue. This article describes a mandibular fibrous osseous dysplasia case and its surgical treatment. A 45-year-old woman complained about a slow development of swelling of the left mandibular bone. The orthopantomography (OPT) and the cone beam computed tomography (CBCT) revealed a well-circumscribed sclerotic lesion with a ground-glass appearance apical to the 3.5 element. The surgery was performed to excise the lesion. Anatomopathological examination of tissue confirmed the suspects among the diagnosis of fibrous dysplasia. The patient underwent to follow-up of 4 years, and no recurrences were found. In the absence of a univocal consensus on therapy, surgery remains the treatment of choice for unifocal forms.

下颌骨纤维性发育不良1例。
纤维发育不良是一种罕见的影响骨组织的遗传综合征。这种病理用结缔组织和纤维组织取代受影响的骨矿化基质。本文报告一下颌纤维性骨性发育不良病例及其手术治疗。45岁女性主诉左下颌骨缓慢肿胀。正体层析成像(OPT)和锥束计算机断层扫描(CBCT)显示一个边界清晰的硬化性病变,具有磨玻璃样外观,顶端至3.5元。手术是为了切除病变。组织的解剖病理检查证实了可疑间纤维发育不良的诊断。随访4年,无复发。在缺乏对治疗的统一共识的情况下,手术仍然是治疗单一形式的选择。
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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CiteScore
1.20
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0.00%
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