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双侧醛固酮分泌性腺瘤:与双侧肾上腺增生的鉴别

Bilateral aldosterone-producing adenomas: differentiation from bilateral adrenal hyperplasia.

作者信息

Wu V C, Chueh S C, Chang H W, Lin W C, Liu K L, Li H Y, Lin Y H, Wu K D, Hsieh B S

机构信息

Clinical Research Building, Department of Internal Medicine, National Taiwan University Hospital, No. 7 Chung-Shan South Road, Taipei 100, Taiwan.

出版信息

QJM. 2008 Jan;101(1):13-22. doi: 10.1093/qjmed/hcm101.

Abstract

BACKGROUND

Primary aldosteronism (PA) is a common curable disease of secondary hypertension. Most such patients have either idiopathic bilateral adrenal hyperplasia (BAH) or unilateral aldosterone-producing adenoma (APA). Bilateral APAs are reportedly extremely rare.

AIM

To compare the distinctive characteristics, clinical course, and outcomes of bilateral APA vs. BAH.

DESIGN

Retrospective record review.

METHODS

From July 1994 to Jan 2007, 190 patients diagnosed with PA underwent surgical intervention at our hospital. Bilateral APA was diagnosed in 7/164 patients with histologically-proven APA. Twenty-one patients diagnosed as BAH, and 21 randomly selected of unilateral APA patients, matched by age and sex served as controls.

RESULTS

Patients with bilateral APA had similar blood pressure, arterial blood gas analysis, spot urinary potassium to creatinine ratio and clinical symptoms to those with BAH, but lower serum potassium levels (p = 0.027), lower plasma renin activity (p = 0.037), and higher plasma aldosterone concentrations (p = 0.029). Aldosterone-renin ratio (ARR) after administration of 50 mg captopril was higher in bilateral APA than in BAH patients (p = 0.023), but not different between unilateral APA and BAH (p = 0.218). A cut-off of ARR >100 ng/dl per ng/ml/h and plasma aldosterone >20 ng/dl after captopril significantly differentiated bilateral APA from BAH. Bilateral subtotal adrenalectomy normalized blood pressure and biochemistry in all patients with bilateral APA.

DISCUSSION

Bilateral APA, presenting simultaneously or sequentially, may not be a rare disease, accounting for 4.3% of APA in this sample. The clinical presentations of bilateral functional adenoma are not different from BAH, but patients with low serum potassium and ARR >100 after captopril should be carefully evaluated for bilateral adenoma.

摘要

背景

原发性醛固酮增多症(PA)是继发性高血压中一种常见的可治愈疾病。大多数此类患者患有特发性双侧肾上腺增生(BAH)或单侧醛固酮分泌腺瘤(APA)。据报道,双侧APA极为罕见。

目的

比较双侧APA与BAH的独特特征、临床病程及预后。

设计

回顾性病历审查。

方法

1994年7月至2007年1月,190例诊断为PA的患者在我院接受手术干预。164例经组织学证实为APA的患者中有7例被诊断为双侧APA。21例被诊断为BAH的患者,以及21例按年龄和性别匹配的随机选择的单侧APA患者作为对照。

结果

双侧APA患者的血压、动脉血气分析、随机尿钾肌酐比值及临床症状与BAH患者相似,但血钾水平较低(p = 0.027),血浆肾素活性较低(p = 0.037),血浆醛固酮浓度较高(p = 0.029)。服用50 mg卡托普利后的醛固酮肾素比值(ARR)在双侧APA患者中高于BAH患者(p = 0.023),但在单侧APA与BAH之间无差异(p = 0.218)。卡托普利给药后ARR>100 ng/dl per ng/ml/h且血浆醛固酮>20 ng/dl可显著区分双侧APA与BAH。双侧肾上腺次全切除术使所有双侧APA患者的血压和生化指标恢复正常。

讨论

双侧APA同时或先后出现,可能并非罕见疾病,在本样本中占APA的4.3%。双侧功能性腺瘤的临床表现与BAH无异,但对于血钾低且卡托普利给药后ARR>100的患者,应仔细评估是否为双侧腺瘤。

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