Komiya I, Takasu N, Aizawa T, Yamada T, Koizumi Y, Hashizume K, Ishihara M, Hiramatsu K, Ichikawa K, Katakura M
J Clin Endocrinol Metab. 1985 Oct;61(4):711-7. doi: 10.1210/jcem-61-4-711.
Seventeen patients with adrenal adenoma causing Cushing's syndrome, eight patients with Cushing's disease due to hypersecretion of ACTH, and five patients with primary aldosteronism due to an aldosteronoma were studied for their computed tomographic (CT) patterns, hormonal profiles, and macroscopic and microscopic findings of the adrenal gland. Black (or brown) adrenal adenomas were found in 71% of the patients with Cushing's syndrome, but not in patients with aldosteronoma. The adrenal tissue of patients with Cushing's disease was predominantly yellow. The number of compact cells was larger in black or brown adenomas than in yellow tumors or hyperplastic adrenal tissue. In patients with Cushing's syndrome, urinary excretion of 17-ketosteroids (17-KS) and serum aldosterone concentrations were lower in those with black or brown adenomas than in those with yellow adenomas (P less than 0.05). Patients with Cushing's disease had even higher 17-KS and serum aldosterone levels. No difference was found in serum cortisol concentrations and dexamethasone suppressibility in two types of adenomas causing Cushing's syndrome. Visual estimation of radiological density of the adrenal tissue relative to the kidney on CT scan and quantitative measurement of it by CT number revealed a difference between the two types of adrenal tumors causing Cushing's syndrome. Adrenal tumors with decreased density on CT scan were yellow adenomas with predominantly clear cells, and those with equal or increased density were black or brown adenomas with predominantly compact cells. All aldosteronomas had decreased density and consisted of clear cells. It is suggested that black or brown adenomas of the adrenal gland have higher radiological density and accompanying lower serum aldosterone and urinary 17-KS levels than ordinary yellow tumors. The abundance of compact cells may have some significance for the development of this particular type of adrenal tumor.
对17例因肾上腺腺瘤导致库欣综合征的患者、8例因促肾上腺皮质激素(ACTH)分泌过多引起库欣病的患者以及5例因醛固酮瘤导致原发性醛固酮增多症的患者,研究了他们的计算机断层扫描(CT)图像特征、激素谱以及肾上腺的大体和显微镜下表现。在71%的库欣综合征患者中发现了黑色(或棕色)肾上腺腺瘤,但醛固酮瘤患者中未发现。库欣病患者的肾上腺组织主要为黄色。黑色或棕色腺瘤中致密细胞的数量比黄色肿瘤或增生性肾上腺组织中的多。在库欣综合征患者中,黑色或棕色腺瘤患者的尿17 - 酮类固醇(17 - KS)排泄量和血清醛固酮浓度低于黄色腺瘤患者(P<0.05)。库欣病患者的17 - KS和血清醛固酮水平甚至更高。引起库欣综合征的两种类型腺瘤在血清皮质醇浓度和地塞米松抑制试验方面未发现差异。通过CT扫描对肾上腺组织相对于肾脏的放射密度进行视觉估计以及通过CT值进行定量测量,发现引起库欣综合征的两种类型肾上腺肿瘤之间存在差异。CT扫描密度降低的肾上腺肿瘤是主要由透明细胞组成的黄色腺瘤,而密度相等或增加的是主要由致密细胞组成的黑色或棕色腺瘤。所有醛固酮瘤密度均降低,且由透明细胞组成。提示肾上腺的黑色或棕色腺瘤比普通黄色肿瘤具有更高的放射密度,同时伴有更低的血清醛固酮和尿17 - KS水平。致密细胞的丰富程度可能对这种特殊类型肾上腺肿瘤的发生具有一定意义。