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痣样基底细胞癌综合征1例报告
引用本文:王茜,潘朝斌,李海刚. 痣样基底细胞癌综合征1例报告[J]. 中国口腔颌面外科杂志, 2007, 5(3): 235-236
作者姓名:王茜  潘朝斌  李海刚
作者单位:1. 中山大学附属第二医院,口腔颌面外科,广东,广州,510120
2. 中山大学附属第二医院,病理科,广东,广州,510120
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疾病,以颌骨多发性角化囊肿、皮肤痣样基底细胞癌及多种骨骼异常为主要临床表现。作者报告1例典型病例.并对其临床、病理和治疗进行了讨论.

关 键 词:痣样基底细胞癌综合征  角化囊肿  成釉细胞瘤
文章编号:1672-3244(2007)03-0235-02
修稿时间:2006-11-272007-02-08

Nevoid basal cell carcinoma syndrome:Report of one case and review of the literature
WANG Qian,PAN Chao-bin,LI Hai-gang. Nevoid basal cell carcinoma syndrome:Report of one case and review of the literature[J]. China Journal of Oral and Maxillofacial Surgery, 2007, 5(3): 235-236
Authors:WANG Qian  PAN Chao-bin  LI Hai-gang
Affiliation:1.Department of Oral trod Maxillofaxlial Surgery,2.Department of Pathology, The Second Affiliated Hospital of Sun Yat-Sen University.Guangzhou 510120. Guangdon,g Province. China
Abstract:
Nevoid basal cell carcinoma syndrome, also known as Gorlin syndrome, is an autosomal dominant inherited disorder which is characterized by the presence of muhiple maxillary keratocysts, facial basal cell carcinomas and some kinds of musculo-skeletal disturbances. This paper reports a typical case of Gorlin syndrome and reviews the relevant literatures regarding to the clinieal and pathological features.
Keywords:Nevoid basal cell carcinoma syndrome   Odontogenic keratoeyst   Ameloblastoma
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