首页> 外文OA文献 >A Rare Case of Preclinical Cushingu27s Syndrome with 'Preclinical' Primary Aldosteronism(Significance of ACTH-loaded adrenal venous sampling in adrenal primary aldosteronism,Proceedings of the 2nd Conference on Adrenal Venous Sampling)
【2h】

A Rare Case of Preclinical Cushingu27s Syndrome with 'Preclinical' Primary Aldosteronism(Significance of ACTH-loaded adrenal venous sampling in adrenal primary aldosteronism,Proceedings of the 2nd Conference on Adrenal Venous Sampling)

机译:罕见的临床前库欣综合征伴“临床前”原发性醛固酮增多症(载有ACTH的肾上腺静脉采样在肾上腺原发性醛固酮增多症中的意义,第二届肾上腺静脉采样会议论文集)

摘要

A rare case of preclinical Cushingu27s syndrome with slight over-production of aldosterone is described. A 54-year-old female patient with a right adrenal mass, 3 cm in diameter on computed tomography, had a history of hypertension for 6 years. The blood pressure was 145/81 mmHg and her plasma potassium level was 3.3 mEq/l. The basal plasma cortisol, ACTH, renin activity and aldosterone levels were within the reference range and the plasma cortisol level was insufficiently suppressed by 8 mg dexamethasone administration. Adrenal venous sampling was performed, which indicated the over-production of both cortisol and aldosterone in the right adrenal tumor. We diagnosed preclinical Cushingu27s syndrome with slight over-production of aldosterone due to the right adrenal tumor and performed right adrenalectomy. Histopathological examination demonstrated a benign adrenocortical adenoma consisting of clear and compact cells. Post-operatively, her blood pressure and plasma potassium level normalized, and her plasma cortisol was sufficiently suppressed by night-time 1 mg dexamethasone administration. The response to captopril load test normalized. In this case, we assume the possibility that the double production of cortisol and aldosterone may reflect disorganized expression of steroidogenic enzymes usually associated with malignant transformation.
机译:描述了罕见的临床前库欣综合征,其醛固酮略有过量产生。一名54岁女性患者,其右肾上腺肿块经计算机断层扫描显示直径为3厘米,有高血压病史达6年。血压为145/81 mmHg,血浆钾水平为3.3 mEq / l。基础血浆皮质醇,促肾上腺皮质激素,肾素活性和醛固酮水平均在参考范围内,而地塞米松8 mg不能充分抑制血浆皮质醇水平。进行肾上腺静脉采样,这表明右肾上腺肿瘤中皮质醇和醛固酮的过量产生。我们诊断为临床前库欣综合征,由于右肾上腺肿瘤导致醛固酮略有过量,并进行了右肾上腺切除术。组织病理学检查显示良性肾上腺皮质腺瘤由透明而致密的细胞组成。术后,血压和血浆钾水平恢复正常,夜间夜间1 mg地塞米松给药可充分抑制血浆皮质醇。对卡托普利负荷试验的反应正常化。在这种情况下,我们假设皮质醇和醛固酮的双重产生可能反映了通常与恶性转化有关的类固醇生成酶的表达紊乱。

相似文献

  • 外文文献
  • 中文文献
  • 专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号