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原发性醛固酮增多症合并亚临床库欣综合征:肾上腺腺瘤的罕见病例报告

Combined primary aldosteronism and preclinical Cushing's syndrome: an unusual case presentation of adrenal adenoma.

作者信息

Honda T, Nakamura T, Saito Y, Ohyama Y, Sumino H, Kurabayashi M

机构信息

Second Department of Internal Medicine, Gunma University School of Medicine, Maebashi, Japan.

出版信息

Hypertens Res. 2001 Nov;24(6):723-6. doi: 10.1291/hypres.24.723.

Abstract

A 55-year-old woman was referred to our institution for evaluation of elevated plasma creatine phosphokinase, hypokalemia and hypertension. Her chief complaints were muscle weakness and polyuria. A left adrenal mass, 4 cm in diameter, was noted on computed tomography. Hormonal assessment demonstrated markedly elevated plasma aldosterone concentration, markedly low plasma renin activity, an abnormal diurnal variation in serum cortisol levels, suppressed baseline plasma adrenocorticotrophic hormone, and non-suppression of serum cortisol by dexamethasone suppression test. She showed no symptoms or signs suggestive of Cushing's syndrome. Adrenal scintigraphy with 131I-6-beta-iodomethyl-norcholesterol showed uptake on the left adrenal and inhibition of the contralateral adrenal gland. She was diagnosed with combined primary aldosteronism and preclinical Cushing's syndrome. Cases of combined primary aldosteronism and preclinical Cushing's syndrome are extremely rare. In patients with large aldosterone-producing adenoma, contralateral adrenal insufficiency should be anticipated after the removal of the tumor.

摘要

一名55岁女性因血浆肌酸磷酸激酶升高、低钾血症和高血压被转诊至我院。她的主要症状是肌肉无力和多尿。计算机断层扫描发现左侧肾上腺有一个直径4厘米的肿块。激素评估显示血浆醛固酮浓度显著升高,血浆肾素活性显著降低,血清皮质醇水平昼夜变化异常,基础血浆促肾上腺皮质激素受抑制,地塞米松抑制试验中血清皮质醇未被抑制。她没有库欣综合征的症状或体征。131I-6-β-碘甲基去甲胆固醇肾上腺闪烁显像显示左侧肾上腺有摄取,对侧肾上腺受抑制。她被诊断为原发性醛固酮增多症合并亚临床库欣综合征。原发性醛固酮增多症合并亚临床库欣综合征的病例极为罕见。对于患有大的醛固酮分泌腺瘤的患者,切除肿瘤后应预期对侧肾上腺功能不全。

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