Clin Nucl Med. 2024 Nov 1;49(11):1027-1030. doi: 10.1097/RLU.0000000000005476. Epub 2024 Sep 25.
A 2-and-a-half-year-old boy with a previous history of Langerhans cell histiocytosis reached remission as assessed by 18 F-FDG PET/CT. Routine follow-up 18 F-FDG PET/CT revealed the appearance of new bone lesions in the right scapula and right ischium with abnormal FDG activity 3 months after the end of treatment, and Langerhans cell histiocytosis recurrence was considered. Meanwhile, these lesions also showed increased FAPI uptake. After adjusting the chemotherapy regimen, both FDG and FAPI uptake almost disappeared in these lesions.
一名 2 岁半的男孩曾患有朗格汉斯细胞组织细胞增生症,经 18 F-FDG PET/CT 评估已缓解。治疗结束后 3 个月,常规 18 F-FDG PET/CT 显示右侧肩胛骨和坐骨出现新的骨病变,伴有异常 FDG 活性,考虑朗格汉斯细胞组织细胞增生症复发。同时,这些病变也显示 FAPI 摄取增加。调整化疗方案后,这些病变中 FDG 和 FAPI 的摄取几乎消失。