Marí C, León J, Farrerons J, Matis-Guiu X, Tembl A, Martin J C, Flotats A, Bernà L l
Nuclear Medicine Department, Hospital Sant Pau, Barcelona, Spain.
J Endocrinol Invest. 1999 Nov;22(10):803-7. doi: 10.1007/BF03343648.
We report a case of a 35-year-old male, with a history of diarrhea, renal lithiasis with frequent expulsions of calculus and hypercalcemia during the last 2 years. The patient was studied and diagnosed with a multiple endocrine neoplasia type I (MEN I), familiar (mother with MEN I). A scintigraphic study with 99mTc-MIBI was performed in order to localize hyperfunctioning parathyroid glands because of biochemical diagnosis of primary hyperparathyroidism. Double phase 99mTc-MIBI scan detected one hyperfunctioning parathyroid gland and a large anterior mediastinal mass. Subsequent, plain radiograph and CT of the chest showed a soft-tissue mass in that localization. Punch biopsy of the lesion guided by CT revealed malignant cells of neuroendocrine tumor. The tumor was removed and histologically confirmed as a carcinoid within a thymus in a MEN type I syndrome. MEN I patients can benefit from the examination with this agent which can potentially localize not only parathyroid endocrine pathology but also unknown associated tumors.
我们报告一例35岁男性病例,该患者有腹泻病史,在过去两年中患有肾结石且频繁排出结石,同时伴有高钙血症。对该患者进行检查后诊断为I型多发性内分泌腺瘤病(MEN I),为家族性(其母亲患有MEN I)。由于原发性甲状旁腺功能亢进的生化诊断,进行了99mTc-MIBI闪烁扫描以定位功能亢进的甲状旁腺。双期99mTc-MIBI扫描检测到一个功能亢进的甲状旁腺和一个巨大的前纵隔肿块。随后,胸部X线平片和CT显示该部位有一个软组织肿块。在CT引导下对病变进行穿刺活检,发现神经内分泌肿瘤的恶性细胞。肿瘤被切除,组织学证实为I型MEN综合征患者胸腺内的类癌。MEN I患者可受益于使用该药物的检查,它不仅有可能定位甲状旁腺内分泌病变,还能定位未知的相关肿瘤。