18F-FDG PET/CT and Whole-Body Bone Scan Findings in Gorlin–Goltz Syndrome
Diagnostics (Basel, Switzerland)(2023)
摘要
Gorlin–Goltz syndrome (basal cell nevus syndromes) is an uncommon, autosomal dominant inherited disorder characterized by developing basal cell carcinomas from a young age. Other distinct clinical features include keratocystic odontogenic tumors, dyskeratotic palmar and plantar pitting, and skeletal abnormalities. Clinicopathological findings of the syndrome are very diverse, and many symptoms manifest during a certain period of life. We present the compelling whole-body bone scan and 18F-FDG PET/CT findings in a 32-year-old man with odontogenic keratocyst, early-onset basal cell carcinoma, multiple ectopic calcifications in extremities, calcified falx cerebri, spinal scoliosis, macrocephaly, and ocular hypertelorism.
更多查看译文
关键词
Gorlin–Goltz syndrome,Gorlin’s syndrome,basal cell nevus syndrome,F-FDG,PET/CT,whole-body bone scan
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要