华西口腔医学杂志

• 病例报告 • 上一篇    下一篇

痣样基底细胞癌综合征家系1例

周晌辉1, 李力力2, 翦新春1, 蒋灿华1   

  1. 1.中南大学湘雅医院口腔颌面外科, 湖南长沙410008; 2.中南大学肿瘤研究所分子生物室, 湖南长沙410078
  • 收稿日期:2008-02-25 修回日期:2008-02-25 出版日期:2008-02-20 发布日期:2008-02-20
  • 通讯作者: 蒋灿华, Tel:0731- 4327113
  • 作者简介:周晌辉(1978-),男,江苏人,博士

A case of nevoid basal cell car cinoma syndrome family

ZHOU Shang- hui1, LI Li- li2, JIAN Xin- chun1, JIANG Can- hua1   

  1. 1. Dept. of Oral and Maxillofacial Surgery, Xiangya Hospital, Central South University, Changsha 410008, China; 2. Molecular Biology Laboratory, Cancer Research Institute, Central South University, Changsha 410078, China
  • Received:2008-02-25 Revised:2008-02-25 Online:2008-02-20 Published:2008-02-20
  • Contact: JIANG Can- hua, Tel:0731- 4327113

摘要:

痣样基底细胞癌综合征是一种罕见的常染色体显性遗传病,以发育异常和肿瘤发生为主要临床特征。本文报告1例痣样基底细胞癌综合征家系,并结合相关文献对该病的发病率、发病机制、临床表现、治疗方法等进行讨论。

关键词: 痣样基底细胞癌综合征, 家系, 牙源性角化囊肿

Abstract:

Nevoid basal cell carcinoma syndrome is a rare autosomal dominant genetic disorder characterized by developmental abnormalities and tumorigenesis. In this paper, a case of nevoid basal cell carcinoma syndrome family was reported, and its incidence, pathogenesis, clinical features and methods of treatment were discussed by reviewing relevant literatures.

Key words: nevoid basal cell carcinoma syndrome, family, odontogenic keratocyst