口腔颌面外科杂志2017，Vol.27Issue(2)：144-149,6.DOI:10.3969/j.issn.1005-4979.2017.02.014
Gardner综合征的病例报告及文献回顾
Gardner Syndrome: Case Report and Review of Literature
蒋瑞芳 1宿玉成 1余立江 1赵大春 2张韬1
作者信息
- 1. 北京协和医院口腔科,北京 100730
- 2. 北京协和医院病理科,北京 100730
- 折叠
摘要
Abstract
Gardner syndrome is featured by a combination of familial adenomatous polyposis (FAP), multiple osteomas and soft tissue tumors. The intestinal polyps have a 100% risk of undergoing malignant transformation, therefore early identifi-cation of this disease is very important. This article reported a case of a 53-year old male patient with Gardner's syndrome, who had intestinal polyps, multiple osteomas in paranasal sinuses and mandible, as well as desmoid tumor of neck. Literatures regarding clinical features, diagnosis, treatment of Gardner syndrome and prevention of related complications were reviewed.关键词
Gardner综合征/家族性腺瘤性息肉病/骨瘤/软组织肿瘤Key words
Gardner syndrome/familial adenomatous polyposis(FAP)/osteomas/soft tissue tumors分类
医药卫生引用本文复制引用
蒋瑞芳,宿玉成,余立江,赵大春,张韬..Gardner综合征的病例报告及文献回顾[J].口腔颌面外科杂志,2017,27(2):144-149,6.
