三种病理并存的下颌骨混合型病变:罕见病例报告并文献复习

A. Verma, J. Dabas, S. Mohanty, A. Urs
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引用次数: 0

摘要

混合型病变是罕见的,显微镜下由不同病理实体的区域组成。双重病变包括中央巨细胞病变(CGCL)和纤维骨性病变的发生已被记录在文献中。虽然许多类似的病例已被报道,但这种病变的病理生理学尚未得到很好的理解。此外,他们的临床行为和治疗指南也没有明确的概述。这里提出一个独特的17岁男性混合性病变与病理实体的三合一,骨化纤维瘤,CGCL和动脉瘤性骨囊肿。临床表现,发病机制和行为报告病变全面解释。作者认为,更多的知识的混合品种的颌骨病变可能有助于更好地理解和管理这些病变的临床医生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Hybrid Lesion of the Mandible with Three Co-existent Pathologies: Report of a Rare Case with Literature Review
Hybrid lesions are rare and microscopically composed of areas of distinct pathologic entities. The occurrence of dual lesions containing Central Giant Cell Lesion (CGCL) and fibro-osseous lesions has been recorded in the literature. Although many similar cases have been reported the pathophysiology of such lesions is yet not well understood. Furthermore, their clinical behaviour and treatment guidelines are also not clearly outlined. Presented here is a unique case of a 17-years old male with a hybrid lesion with a triad of pathological entities, Ossifying fibroma, CGCL and aneurysmal bone cyst. The clinical presentation, pathogenesis and behaviour of the reported lesion are comprehensively explained. The authors believe that greater knowledge of the hybrid variety of jaw lesions may aid in better understanding and management of these lesions by clinicians.
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