首页> 美国卫生研究院文献>Anais Brasileiros de Dermatologia >Syndrome in question: Gorlin-Goltz syndrome
【2h】

Syndrome in question: Gorlin-Goltz syndrome

机译:所讨论的综合症:Gorlin-Goltz综合症

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The Nevoid Basal Cell Carcinoma Syndrome (NBCCS) is an uncommon disorder caused by a mutation in Patched, tumor suppressor gene. It is mainly characterized by numerous early onset basal cell carcinomas, odontogenic cysts of jaw and skeletal abnormalities. Due to the wide clinical spectrum, treatment and management of its modalities are not standardized and should be individualized and monitored by a multidisciplinary team. We report a typical case in a 30-year-old man with multiple basal cell carcinomas, keratotic pits of palmar creases and bifid ribs, with a history of several corrective surgeries for keratocystic odontogenic tumors, among other lesions characteristic of the syndrome.
机译:Nevoid基底细胞癌综合症(NBCCS)是一种罕见的疾病,由修补的抑癌基因突变引起。它的主要特征是许多早期发作的基底细胞癌,颌骨牙源性囊肿和骨骼异常。由于临床范围很广,其模式的治疗和管理尚不规范,应由多学科团队进行个性化和监控。我们报道了一名30岁男子的典型病例,该男子患有多种基底细胞癌,掌状折痕和双裂肋的角化性凹痕,并有一些针对角膜囊性牙源性肿瘤的矫正手术史,以及该综合征的其他病变。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号