口腔医学研究 ›› 2025, Vol. 41 ›› Issue (4): 345-347.DOI: 10.13701/j.cnki.kqyxyj.2025.04.013

• 病例报告 • 上一篇    下一篇

基底细胞痣综合征1例

叶峥, 隋馥勇, 徐冰宁, 张福胤*   

  1. 大连医科大学附属第二医院口腔颌面外科 辽宁 大连 116000
  • 收稿日期:2024-06-28 发布日期:2025-04-24
  • 通讯作者: * 张福胤,E-mail:dentistsui@163.com
  • 作者简介:叶峥(1998~ ),男,内蒙古人,硕士在读,研究方向:口腔颌面外科学。
  • 基金资助:
    大连医科大学附属第二医院临床能力提升“1+X”计划交叉学科创新项目(2022JCXKYB24)

Basal Cell Nevus Syndome: A Case Report

YE Zheng, SUI Fuyong, XU Bingning, ZHANG Fuyin*   

  1. Department of Oral and Maxillofacial Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian 116000, China
  • Received:2024-06-28 Published:2025-04-24

摘要: 基底细胞痣综合征(basal cell nevus syndrome, BCNS)是一种极其少见的常染色体显性遗传疾病,其在口腔颌面部最常表现为牙源性角化囊肿(odontogenic keratocyst,OKC),同时在不同时期会出各类相关疾病。本文报告1例BCNS,并结合相关文献进行讨论,为临床诊疗提供参考。

关键词: 基底细胞痣综合征, 牙源性角化囊肿, 颅内钙化

Abstract: Basal cell nevus syndrome (BCNS) is a rare autosomal dominant disorder, which is most often manifested as odontogenic keratocysts (OKC) in the oral and maxillofacial region, and various related diseases may occur at different times of the patient's life. This paper reports a cases of basal cell nevus syndrome and discusses them with related literature to provide reference for clinical diagnosis and treatment.

Key words: basal cell nevus syndrome, odontogenic keratocyst, intracranial calcification