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大型成釉细胞纤维瘤的治疗:一例报告。

Treatment of large ameloblastic fibroma: a case report.

作者信息

Vasconcelos Belmiro C E, Andrade Emanuel S S, Rocha Nelson S, Morais Hécio H A, Carvalho Ricardo W F

机构信息

Department of Oral and Maxillofacial Surgery, Pernambuco School of Dentistry, University of Pernambuco, Recife, Brazil.

出版信息

J Oral Sci. 2009 Jun;51(2):293-6. doi: 10.2334/josnusd.51.293.

Abstract

Ameloblastic fibroma (AF) is an extremely rare true mixed benign tumor that can occur in either the mandible or the maxilla, but is most frequently found in the posterior region of the mandible. It usually occurs in the first two decades of life and is associated with tooth enclosure, causing a delay in eruption or altering the dental eruption sequence. AF is diagnosed on routine radiographic evaluation and is clinically and radiographically similar to ameloblastic fibrodontoma and odontoma, which makes an accurate diagnosis mandatory. There is controversy in the literature as to whether treatment should be conservative or agressive. A conservative treatment strategy, such as enucleation and curettage, is usually sufficient. However, extensive lesions require radical treatment. We describe a case of ameloblastic fibroma with a very unusual clinical manifestation: it demonstrated considerable extension but no associated impacted tooth, was located in the anterior region of the mandible, and became symptomatic in the fifth decade of life. A radical surgical approach was taken, with immediate reconstruction.

摘要

成釉细胞纤维瘤(AF)是一种极为罕见的真正的混合性良性肿瘤,可发生于下颌骨或上颌骨,但最常见于下颌骨后部。它通常发生在生命的前二十年,与牙齿包绕有关,导致牙齿萌出延迟或改变牙齿萌出顺序。AF通过常规影像学评估进行诊断,在临床和影像学上与成釉细胞纤维牙瘤和牙瘤相似,因此必须进行准确诊断。关于治疗应保守还是积极,文献中存在争议。保守的治疗策略,如摘除术和刮除术,通常就足够了。然而,广泛的病变需要根治性治疗。我们描述了一例成釉细胞纤维瘤,其临床表现非常不寻常:它显示出相当大的范围,但没有相关的阻生牙,位于下颌骨前部,在生命的第五个十年出现症状。采用了根治性手术方法,并立即进行了重建。

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