Otsuka F, Ogura T, Nakao K, Hayakawa N, Mimura Y, Yamauchi T, Makino H
Department of Medicine III, Okayama University Medical School.
Intern Med. 1998 Apr;37(4):385-90. doi: 10.2169/internalmedicine.37.385.
A 49-year-old woman with Cushing's syndrome due to unilateral adrenal hyperplasia is presented. She had developed obesity and menopause for 2 years, but no hypertension or hypertrichosis was observed. Although plasma adrenocorticotropin and serum cortisol levels were within normal ranges, the circadian rhythm has completely disappeared. Free thyroxine and triiodothyronine levels were decreased. Adrenocorticotropin did not respond to corticotropin-releasing hormone, and urinary excretion of 17-hydroxycorticosteroids was not suppressed by dexamethasone. Abdominal computed tomography and 131I-Adosterol scintigraphy demonstrated a unilateral functioning mass in the left adrenal gland. The resected left adrenal mass was pathologically diagnosed as the rare condition of adrenocortical nodular hyperplasia.
本文报告了一名49岁因单侧肾上腺增生导致库欣综合征的女性患者。她出现肥胖和绝经2年,但未观察到高血压或多毛症。尽管血浆促肾上腺皮质激素和血清皮质醇水平在正常范围内,但昼夜节律已完全消失。游离甲状腺素和三碘甲状腺原氨酸水平降低。促肾上腺皮质激素对促肾上腺皮质激素释放激素无反应,地塞米松未抑制17-羟皮质类固醇的尿排泄。腹部计算机断层扫描和131I-阿多甾醇闪烁显像显示左肾上腺有一个单侧功能性肿块。切除的左肾上腺肿块经病理诊断为罕见的肾上腺皮质结节性增生。