Barliev G B
Eur J Nucl Med. 1979 Dec;4(6):449-51. doi: 10.1007/BF00300844.
Seven patients with Cushing's syndrome secondary to adrenocortical tumors were studied using 131I-19-iodocholesterol. The diagnosis of all cases were verified histologically. In three cases with adenoma the uptake of the tracer was in the tumor only, while the two patients with adrenocortical carcinoma failed to show adrenal accumulation of the labelled compound. In two patients there was a hyperplasia-like scintigraphic pattern, while the stimulation and suppression biochemical tests suggested adrenal tumor. One of these cases was verified as a mixed form (adenoma plus hyperplasia), and the tumor bearing gland was significantly larger on the scan which helped the preoperative localization. In the other case, verified as bilateral multiple adrenocortical adenomas, the autonomus function of both adrenals was proved by dexamethasone suppression scanning. It seens reasonable to use the latter as an adunctive diagnostic procedure in patients where there is a discrepancy between the standart scintiscan and the biochemical indexes of adrenal hyperfunction.
对7例肾上腺皮质肿瘤继发库欣综合征的患者使用131I-19-碘胆固醇进行了研究。所有病例的诊断均经组织学证实。3例腺瘤患者中,示踪剂仅在肿瘤中摄取,而2例肾上腺皮质癌患者未显示标记化合物在肾上腺的积聚。2例患者有类似增生的闪烁显像模式,而刺激和抑制生化试验提示肾上腺肿瘤。其中1例经证实为混合形式(腺瘤加增生),扫描显示肿瘤所在腺体明显增大,这有助于术前定位。另一例经证实为双侧多发性肾上腺皮质腺瘤,地塞米松抑制扫描证实双侧肾上腺均有自主功能。对于标准闪烁扫描与肾上腺功能亢进生化指标存在差异的患者,将后者用作辅助诊断程序似乎是合理的。