Ly Justin Q, Beall Douglas P
Department of Radiology and Nuclear Medicine, Wilford Hall Medical Center, San Antonio, Texas, USA.
Australas Radiol. 2003 Sep;47(3):318-21. doi: 10.1046/j.1440-1673.2003.01186.x.
Gorlin's syndrome (also known as basal cell nevus syndrome, Gorlin-Goltz syndrome, and nevoid basal cell carcinoma syndrome) is a rare, inherited disorder characterized by multiple basal-cell epitheliomas, intracranial calcification, keratocysts of the mandible, and unusual and striking skeletal abnormalities. We present the interesting case of a 45-year-old woman who was informed that she had fibrous dysplasia of the extremity at another institution before extensive radiological work-up showed a diffuse skeletal process. The skeletal abnormalities, in conjunction with the patient's history of multiple basal cell carcinomas, is consistent with the diagnosis of Gorlin's syndrome. We describe this unusual case of striking radiological and scintigraphic findings in a patient with Gorlin's syndrome.
戈林综合征(也称为基底细胞痣综合征、戈林-戈尔茨综合征和痣样基底细胞癌综合征)是一种罕见的遗传性疾病,其特征为多发性基底细胞上皮瘤、颅内钙化、下颌骨角化囊肿以及异常显著的骨骼异常。我们报告了一例有趣的病例,一名45岁女性在另一家机构被诊断为肢体纤维发育不良,而广泛的放射学检查显示为弥漫性骨骼病变。骨骼异常,结合患者多发基底细胞癌的病史,符合戈林综合征的诊断。我们描述了该例戈林综合征患者显著的放射学和闪烁扫描结果的罕见病例。