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Gigantiform cementoma of the mandible: case report and literature review

机译:下颌骨Gigantiform牙骨质瘤:病例报告和文献复习

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摘要

The gigantiform cementoma (GC) is an extremely rare, benign condition of fibro-cemento-osseous origin that is noted in the jaws, more commonly in younger individuals. Both sporadic cases of GC and those with an autosomal dominant pattern of inheritance have been reported in the English literature. There exists a great deal of overlap and confusion between GC and other benign, reactive or neoplastic fibro-osseous lesions, especially florid cement-osseous dysplasia and ossifying fibroma. The GC typically presents as a multiquadrant, expansile, mixed radiolucent-opaque lesions that frequently cross the midline of the jaws. We report a case of GC in a 41-year-old Haitian female. Clinical, radiographic, and microscopic features of this condition are presented, along with criteria to differentiate GC from other fibro-osseous diseases of the jaws. A brief review of the literature with clinical, radiographic findings and treatment recommendation is discussed. Additional cases of GC, as well as further investigation of the genes that may be involved, are needed to further understand this rare entity.
机译:巨人胶质瘤(GC)是纤维-水泥骨起源的一种极为罕见的良性疾病,在下颌中可见,在年轻人中更为常见。在英国文献中,既有零星的GC病例,也有常染色体显性遗传的病例。 GC与其他良性,反应性或赘生性纤维骨病变,特别是小花样骨水泥性不典型增生和骨化性纤维瘤之间存在大量重叠和混淆。 GC通常表现为多象限,可扩张,混合的不透射线的,不透明的病变,经常穿过颌骨中线。我们报告了一名41岁的海地女性GC的病例。介绍了这种情况的临床,影像学和微观特征,以及区分GC与其他颌骨纤维性骨疾病的标准。讨论了对具有临床,影像学发现和治疗建议的文献的简要回顾。需要GC的其他案例以及可能涉及的基因的进一步研究,以进一步了解这种稀有实体。

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