以牙源性黏液瘤为表现的Gardner综合征的颌面x线摄影研究:一例罕见病例报告。

Q2 Dentistry
Stomatologija Pub Date : 2018-01-01
Loutfi Salti, Michael Rasse, Khaled Al-Ouf
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引用次数: 0

摘要

加德纳综合征是一种常染色体显性遗传病。它的特点是肠道家族性腺瘤性息肉病(FAP)合并肠外病变,如多发性骨瘤和纤维瘤。牙源性黏液瘤是一种良性的、侵袭性的骨内肿瘤。我们报告一个罕见的病例,14岁的男性患者加德纳综合征和牙源性黏液瘤,涉及整个下颌骨的左半部分,导致严重的面部畸形,在一年的时间内。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Maxillofacial Radiographic study of Gardner's syndrome presenting with odontogenic myxoma: A rare case report.

Gardner syndrome is an autosomal dominant disease. It is characterized by a combination of familial adenomatous polyposis (FAP) of the intestine with extraintestinal changes as multiple osteomas and fibromas. Odontogenic Myxoma is a benign, aggressive intraosseous neoplasm. We report a rare case of a 14-year-old male patient with Gardner's syndrome and odontogenic myxoma, which involved the entire left half of the mandible, resulting in a gross facial deformity, within a span of one year.

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来源期刊
Stomatologija
Stomatologija Medicine-Medicine (all)
CiteScore
1.10
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