Zheng Chengcheng, Zhao Lianling, Zheng Chang, Ren Yan, Tian Haoming, Chen Tao
Department of Endocrinology and Metabolism, West China Hospital, Sichuan University, Chengdu, China.
Department of Endocrinology, The First People's Hospital of Guiyang, Guiyang, China.
Gland Surg. 2022 Jan;11(1):279-284. doi: 10.21037/gs-21-607.
Aldosterone-to-renin ratio is the most reliable screening method of primary aldosteronism and has been widely used in clinical practice, but the index is influenced by many factors, some of which cause it false-negative, consequently leading to primary aldosteronism underdiagnosed. We report a rare case of a 27-year-old woman complaining of elevated arterial blood pressure and spontaneous hypokalemia but whose aldosterone-to-renin ratio were negative consecutively. She also had symptoms of polydipsia and polyuria for more than 20 years, with the volume of water intake and urine output up to 17 liters per day. Confirmatory tests of saline infusion test and captopril challenge test could not suppress plasma aldosterone concentration to the cutoff value. Abdominal contrast-enhanced CT suggested an adenoma on the right adrenal gland. After excluding other known causes of hypertension with hypokalemia, the patient was ultimately diagnosed with aldosterone-producing adenoma complicated with primary polydipsia. Complete clinical remission was achieved after unilateral adrenalectomy. The histopathology showed typical features of adrenocortical adenoma which was positive for CYP11B2 by immunohistochemistry, and next-generation sequencing results of tumor tissues revealed a missense mutation of the gene [chr11:128781619, c.451 (exon 2) G>A]. All these findings supported the diagnosis of aldosterone-producing adenoma. This study has shown that negative aldosterone-to-renin ratio screening result cannot simply exclude primary aldosteronism. Comprehensive patient's evaluation should be taken to avoid missed diagnosis in clinical work, especially for those who have potentially curative surgery.
醛固酮与肾素比值是原发性醛固酮增多症最可靠的筛查方法,已在临床实践中广泛应用,但该指标受多种因素影响,其中一些因素会导致其出现假阴性,从而导致原发性醛固酮增多症诊断不足。我们报告了一例罕见病例,一名27岁女性,主诉动脉血压升高和自发性低钾血症,但其醛固酮与肾素比值连续呈阴性。她还有多饮多尿症状20多年,每日饮水量和尿量高达17升。生理盐水输注试验和卡托普利激发试验的确诊试验均不能将血浆醛固酮浓度抑制至临界值。腹部增强CT提示右肾上腺有一个腺瘤。在排除其他已知的低钾血症性高血压病因后,该患者最终被诊断为醛固酮瘤合并原发性烦渴。单侧肾上腺切除术后实现了完全临床缓解。组织病理学显示肾上腺皮质腺瘤的典型特征,免疫组化显示CYP11B2阳性,肿瘤组织的二代测序结果显示该基因存在错义突变[chr11:128781619,c.451(外显子2)G>A]。所有这些发现均支持醛固酮瘤的诊断。本研究表明,醛固酮与肾素比值筛查结果为阴性不能简单排除原发性醛固酮增多症。在临床工作中应进行全面的患者评估以避免漏诊,尤其是对于那些有潜在治愈性手术的患者。