Kim Jee-Woo, Ko Jung Min, Lee Dong Yoon, Shin Jung-Won
Department of Dermatology, Seoul National University Bundang Hospital, Seongnam, Korea.
Department of Pediatrics, Seoul National University Children's Hospital, Seoul, Korea.
Ann Dermatol. 2023 May;35(Suppl 1):S19-S24. doi: 10.5021/ad.20.320.
Rubinstein-Taybi syndrome (RSTS) is an extremely rare genetic disorder affecting multi-organ systems. A tendency to form keloid is one of the common dermatologic manifestations. We describe a 23-year-old female presented with extensive keloids which developed spontaneously. She had typical facial features, broad thumbs, and dental defects, which were suspicious features of genetic syndrome. Direct sequencing for cyclic-AMP-regulated enhancer binding protein revealed a novel mutation. So far, 23 cases of RSTS have been reported in Korean literature. To the best of our knowledge, this is the first report in Korea to describe confirmed case of RSTS with extensive keloids as a chief manifestation.
鲁宾斯坦-泰比综合征(RSTS)是一种极其罕见的影响多器官系统的遗传性疾病。形成瘢痕疙瘩的倾向是常见的皮肤表现之一。我们描述了一名23岁女性,她出现了广泛的自发性瘢痕疙瘩。她具有典型的面部特征、宽阔的拇指和牙齿缺陷,这些都是遗传综合征的可疑特征。对环磷酸腺苷调节的增强子结合蛋白进行直接测序发现了一种新的突变。到目前为止,韩国文献中已报道23例RSTS病例。据我们所知,这是韩国首例以广泛瘢痕疙瘩为主要表现的确诊RSTS病例报告。