From the Departments of Nuclear Medicine.
Surgery.
Clin Nucl Med. 2024 Sep 1;49(9):e451-e452. doi: 10.1097/RLU.0000000000005308. Epub 2024 May 31.
A 17-year-old boy with Von Hippel-Lindau syndrome presented with hypertension, raised plasma catecholamines, and MRI findings of a new pancreatic tail lesion and 2 stable right adrenal lesions concerning for functional neuroendocrine tumors. A 68 Ga-DOTATATE PET/CT demonstrated intense tracer avidity within the pancreatic lesion with minimal uptake in the adrenal lesions. Conversely, a 123 I-MIBG SPECT/CT study demonstrated high-grade tracer uptake within the adrenal lesions, with no significant uptake appreciated in the pancreatic lesion. The adrenal lesions were resected, and pathology was consistent with pheochromocytoma. Plasma catecholamines returned to within the normal range and hypertension resolved.
一位患有冯·希佩尔-林道综合征的 17 岁男孩因高血压、血浆儿茶酚胺升高以及 MRI 检查发现新的胰尾病变和 2 个稳定的右侧肾上腺病变而就诊,这些病变提示功能性神经内分泌肿瘤。68Ga-DOTATATE PET/CT 显示胰尾病变部位有强烈的示踪剂摄取,而肾上腺病变部位摄取较少。相反,123I-MIBG SPECT/CT 研究显示肾上腺病变部位有高浓度示踪剂摄取,而胰尾病变部位无明显摄取。肾上腺病变被切除,病理结果符合嗜铬细胞瘤。血浆儿茶酚胺恢复正常范围,高血压得到缓解。