Galloway Terrel L, Johnston Mickaila J, Starsiak Michael D, Silverman Eugene D
Department of Radiology, Division of Nuclear Medicine, Naval Medical Center San Diego, San Diego, California, USA.
World J Nucl Med. 2017 Jan-Mar;16(1):59-61. doi: 10.4103/1450-1147.176886.
A case of a 7-month-old white female who was referred for 18F-fluorodeoxyglucose (FDG) Positron emission tomography/computed tomography (PET/CT) initial evaluation of a lytic skull lesion with presumed diagnosis of Langerhans cell histiocytosis is described. Incidentally, she was found to have hypermetabolic nodules in the soft tissues of her anterior thighs.
一名7个月大的白人女性因颅骨溶骨性病变接受18F-氟脱氧葡萄糖(FDG)正电子发射断层扫描/计算机断层扫描(PET/CT)初步评估,初步诊断为朗格汉斯细胞组织细胞增多症。偶然发现,她的大腿前部软组织中有高代谢结节。