Department of Surgical Sciences, Uppsala University, SE-751 85 Uppsala, Sweden.
Langenbecks Arch Surg. 2010 Sep;395(7):963-7. doi: 10.1007/s00423-010-0681-7. Epub 2010 Jul 20.
To evaluate whether dexamethasone suppression treatment can improve (11) C-metomidate positron emission tomography (MTO-PET) detection of small adrenocortical adenomas in primary aldosteronism (PA).
Eleven patients with proven PA and two patients with non-hyperfunctioning adrenocortical incidentalomas and small adrenocortical tumours observed on CT underwent MTO-PET before and 3 days after administration of oral dexamethasone suppression treatment. Small "hot-spot" regions of interest comprising 4 pixels (SUVhs) and 1 pixel (SUVmax) were placed in the tumour area with the highest radioactivity concentration and their respective standardised uptake values (SUV) were recorded.
All tumours were detected and categorised as adrenocortical by MTO-PET. SUVhs as well as SUVmax were higher in PA compared to nonfunctional adenomas. Normal adrenal cortex was suppressed after dexamethasone (p < 0.05), but tumour SUV was not significantly decreased after suppression in either PA or nonfunctional tumours (p > 0.05). However, these changes caused no significant increase in the tumour-to-normal adrenal ratio (p > 0.05).
MTO-PET is a highly sensitive method for detecting and categorising even small adrenocortical tumours in PA. In this series, dexamethasone-suppressed MTO-PET was unable to increase the tumour-to-normal adrenal ratio to further facilitate detection of small adenomas in PA as an alternative to adrenal venous sampling.
评估地塞米松抑制治疗是否能提高(11)C-美托咪定正电子发射断层扫描(MTO-PET)对原发性醛固酮增多症(PA)中小肾上腺皮质腺瘤的检测。
11 例经证实的 PA 患者和 2 例无功能肾上腺偶然瘤和 CT 观察到的小肾上腺皮质肿瘤患者,在口服地塞米松抑制治疗前和治疗后 3 天进行 MTO-PET。将 4 个像素(SUVhs)和 1 个像素(SUVmax)的小“热点”感兴趣区置于放射性浓度最高的肿瘤区域,并记录各自的标准化摄取值(SUV)。
所有肿瘤均通过 MTO-PET 检测并分类为肾上腺皮质肿瘤。PA 患者的 SUVhs 和 SUVmax 均高于无功能腺瘤。地塞米松抑制后正常肾上腺皮质被抑制(p<0.05),但 PA 或无功能肿瘤抑制后肿瘤 SUV 无明显降低(p>0.05)。然而,这些变化并没有导致肿瘤与正常肾上腺的比值显著增加(p>0.05)。
MTO-PET 是一种高度敏感的方法,可用于检测和分类 PA 中甚至小的肾上腺皮质肿瘤。在本系列中,地塞米松抑制后的 MTO-PET 未能增加肿瘤与正常肾上腺的比值,无法作为肾上腺静脉取样的替代方法来进一步提高对 PA 中小腺瘤的检测。