Baron F, Sprauve M E, Huddleston J F, Fisher A J
Department of Gynecology and Obstetrics, Emory University School of Medicine, Atlanta, Georgia, USA.
Obstet Gynecol. 1995 Oct;86(4 Pt 2):644-5. doi: 10.1016/0029-7844(95)00208-9.
Aldosterone-producing adrenal adenomas are rare, especially during pregnancy. We report a patient who presented in the early second trimester, was diagnosed with primary aldosteronism, and was treated successfully by adrenalectomy.
A 17-year-old black nulliparous woman was found to have a blood pressure (BP) of 150/82 mmHg when she registered for prenatal care at 14 weeks' gestation. Initial laboratory assessment revealed a markedly diminished serum potassium level of 2.1 mmol/L. Further laboratory evaluation detected decreased random plasma renin activity and an elevated aldosterone level. Magnetic resonance imaging revealed a 2-cm right adrenal lesion. She was diagnosed with an adrenal adenoma and successfully underwent an adrenalectomy at 17 weeks' gestation. Postoperatively, her BP and serum potassium level normalized. She spontaneously delivered a normal male infant at term.
Although primary hyperaldosteronism is a rare clinical entity, it must be considered when hypertension and hypokalemia are present concurrently. Antepartum medical management can be difficult, often resulting in poor obstetric outcome. Surgery in the second trimester is an effective option.
分泌醛固酮的肾上腺腺瘤较为罕见,尤其是在孕期。我们报告一例患者,在孕中期早期就诊,被诊断为原发性醛固酮增多症,并通过肾上腺切除术成功治愈。
一名17岁未生育的黑人女性,在妊娠14周登记进行产前检查时,血压(BP)为150/82 mmHg。初始实验室评估显示血清钾水平显著降低,为2.1 mmol/L。进一步的实验室检查发现随机血浆肾素活性降低,醛固酮水平升高。磁共振成像显示右侧肾上腺有一个2厘米的病变。她被诊断为肾上腺腺瘤,并在妊娠17周时成功接受了肾上腺切除术。术后,她的血压和血清钾水平恢复正常。她足月自然分娩了一名健康男婴。
虽然原发性醛固酮增多症是一种罕见的临床病症,但当同时出现高血压和低钾血症时必须予以考虑。产前的药物治疗可能困难,常常导致不良的产科结局。孕中期进行手术是一种有效的选择。