双侧齿状成釉纤维瘤1例

A. Bakhil, Nawfal El Hafdi, Y. Ribag, Hicham Sabani, L. Khalfi, J. Hamama, K. E. Khatib
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引用次数: 0

摘要

成釉细胞纤维瘤是一种罕见的混合性牙源性肿瘤,多见于年轻人群,其治疗主要以手术为主。我们在这项工作中报告了首次观察到的伴随双颌定位。临床观察:这是一位31岁的女性患者,无病理史,因上颌下颌骨肿瘤来我科就诊。临床检查发现口腔状况不佳及牙槽嵴肿胀。面部肿块的CT扫描显示一个多室囊性病变,包括上颌和下颌的牙齿。活组织检查结果显示是牙髓成釉细胞纤维瘤。治疗包括根治性切除和局部皮瓣重建。FOA是一种不同于成釉细胞瘤的肿瘤,多发于年轻患者,无性别差异。影像学表现为单室或多室囊性影像,与其他囊性肿瘤的鉴别诊断存在困难。治疗是手术,临床和放射术后监测是首要的考虑到复发或肉瘤转化的风险。结论:FOA长期以来被认为是成釉细胞瘤的一种形式,是一种罕见的肿瘤,在下颌定位最常见,双颌定位从未被描述过,我们报道的病例在文献中是第一例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bimaxillary odonto-ameloblastic fibroma: A case report
Introduction: Ameloblastic fibroma is a rare mixed odontogenic tumor, affects the young population, its management is mainly surgical. We report in this work the first observation of a concomitant bimaxillary localization. Clinical observation: This is a 31-year-old female patient with no pathological history who presented to our department for management of a maxillomandibular tumor. The clinical examination revealed a poor oral condition and a swelling of the alveolar ridges. The CT scan of the facial mass revealed a multilocular cystic lesion encompassing teeth in the maxillary and mandibular bone. The biopsy came back in favor of an odontoameloblastic fibroma. Management consisted of radical resection with reconstruction using local flaps. FOA is a tumor distinct from ameloblastoma, it affects the young patients without any predilection to gender. The radiological image is a mono or multilocular cystic image which poses a problem of differential diagnosis with other cystic tumors. The management is surgical, clinical and radiological postoperative surveillance is primordial given the risk of recurrence or sarcomatous transformation. Conclusion: The FOA was for a long time considered as a form of ameloblastoma, is a rare tumor in the mandibular localization is the most frequent, the bimaxillary localization has never been described and the case we presented is the first in literature.  
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