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原发性醛固酮增多症:亚型分类面临的挑战

Primary hyperaldosteronism: challenges in subtype classification.

作者信息

Layden Brian T, Hahr Allison J, Elaraj Dina M

机构信息

Division of Endocrinology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

出版信息

BMC Res Notes. 2012 Oct 30;5:602. doi: 10.1186/1756-0500-5-602.

DOI:10.1186/1756-0500-5-602
PMID:23110780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3522539/
Abstract

BACKGROUND

Primary hyperaldosteronism (PA) is a serious and potentially debilitating disease. Detailed guidelines have been written to guide endocrinologists in establishing the diagnosis of PA as well as in subtype classification of PA. The objective of this case report is to present a case where subtype classification of PA was challenging and repeated imaging of the adrenal glands helped establish the diagnosis in a patient with initial normal adrenal glands on CT and MRI images.

CASE PRESENTATION

We report a case of a 29-year-old woman with an established diagnosis of PA, but unclear subtype, who presented to us for further management. She initially presented for medical evaluation of uncontrolled hypertension and spontaneous hypokalemia 4 years prior. In the investigation of secondary causes of hypertension, plasma aldosterone-to-plasma renin activity ratio was elevated on two separate occasions, and primary hyperaldosteronism was confirmed by saline infusion test. Also during this time, she had adrenal venous sampling done 3 times at multiple institutions yielding confusing results. Initially, imaging by CT and MRI showed normal adrenal glands. To help establish the subtype of PA, we reimaged this patient's adrenal glands one year later revealing a 2 cm left adrenal adenoma. Laparoscopic left adrenalectomy improved her hypertension and was curative of her hypokalemia.

CONCLUSION

This case presents an unusual case where reimaging of the adrenal glands led to the discovery of a single adenoma, initially not observed on imaging studies.

摘要

背景

原发性醛固酮增多症(PA)是一种严重且可能使人衰弱的疾病。已经制定了详细的指南,以指导内分泌科医生进行PA的诊断以及PA的亚型分类。本病例报告的目的是介绍一例PA亚型分类具有挑战性的病例,肾上腺的重复成像有助于对一名CT和MRI图像上肾上腺最初正常的患者进行诊断。

病例介绍

我们报告一例29岁已确诊PA但亚型不明的女性患者,她前来我们这里寻求进一步治疗。她最初是在4年前因无法控制的高血压和自发性低钾血症前来进行医学评估的。在对高血压的继发原因进行调查时,血浆醛固酮与血浆肾素活性比值在两个不同时间点升高,盐水输注试验证实了原发性醛固酮增多症。在此期间,她还在多家机构进行了3次肾上腺静脉采样,结果令人困惑。最初,CT和MRI成像显示肾上腺正常。为了帮助确定PA的亚型,我们在一年后对该患者的肾上腺进行了再次成像,发现左侧肾上腺有一个2厘米的腺瘤。腹腔镜下左侧肾上腺切除术改善了她的高血压,并治愈了她的低钾血症。

结论

本病例呈现了一种不寻常的情况,即肾上腺的再次成像导致发现了一个最初在影像学检查中未观察到的单一腺瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8659/3522539/6311d6564056/1756-0500-5-602-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8659/3522539/6311d6564056/1756-0500-5-602-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8659/3522539/6311d6564056/1756-0500-5-602-1.jpg

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本文引用的文献

1
The Adrenal Vein Sampling International Study (AVIS) for identifying the major subtypes of primary aldosteronism.用于确定原发性醛固酮增多症主要亚型的肾上腺静脉采样国际研究(AVIS)。
J Clin Endocrinol Metab. 2012 May;97(5):1606-14. doi: 10.1210/jc.2011-2830. Epub 2012 Mar 7.
2
Discrepant results of adrenal venous sampling in seven patients with primary aldosteronism.7 例原发性醛固酮增多症患者肾上腺静脉采血结果不一致。
Kidney Blood Press Res. 2012;35(4):205-10. doi: 10.1159/000330720. Epub 2012 Jan 3.
3
Primary aldosteronism in 2011: Towards a better understanding of causation and consequences.
妊娠期肾素瘤与肾上腺腺瘤并存:一例报告。
Oncol Lett. 2017 May;13(5):3186-3190. doi: 10.3892/ol.2017.5802. Epub 2017 Mar 3.
4
Incidental adrenal enlargement: an overview from a retrospective study in a chinese population.偶然发现的肾上腺增大:一项中国人群回顾性研究综述。
Int J Endocrinol. 2015;2015:192874. doi: 10.1155/2015/192874. Epub 2015 Mar 8.
2011 年原发性醛固酮增多症:对病因和后果认识的进一步提高。
Nat Rev Endocrinol. 2011 Dec 13;8(2):70-2. doi: 10.1038/nrendo.2011.223.
4
Glucocorticoid-remediable aldosteronism.糖皮质激素可治性醛固酮增多症。
Endocrinol Metab Clin North Am. 2011 Jun;40(2):333-41, viii. doi: 10.1016/j.ecl.2011.01.012.
5
K+ channel mutations in adrenal aldosterone-producing adenomas and hereditary hypertension.肾上腺醛固酮产生腺瘤和遗传性高血压中的 K+ 通道突变。
Science. 2011 Feb 11;331(6018):768-72. doi: 10.1126/science.1198785.
6
Endocrine hypertension: then and now.内分泌性高血压:过去与现在。
Endocr Pract. 2010 Sep-Oct;16(5):888-902. doi: 10.4158/EP10205.RA.
7
What are the keys to successful adrenal venous sampling (AVS) in patients with primary aldosteronism?原发性醛固酮增多症患者成功进行肾上腺静脉采血(AVS)的关键是什么?
Clin Endocrinol (Oxf). 2009 Jan;70(1):14-7. doi: 10.1111/j.1365-2265.2008.03450.x.
8
Case detection, diagnosis, and treatment of patients with primary aldosteronism: an endocrine society clinical practice guideline.原发性醛固酮增多症患者的病例发现、诊断及治疗:内分泌学会临床实践指南
J Clin Endocrinol Metab. 2008 Sep;93(9):3266-81. doi: 10.1210/jc.2008-0104. Epub 2008 Jun 13.
9
The aldosteronoma resolution score: predicting complete resolution of hypertension after adrenalectomy for aldosteronoma.醛固酮瘤消退评分:预测醛固酮瘤肾上腺切除术后高血压的完全消退
Ann Surg. 2008 Mar;247(3):511-8. doi: 10.1097/SLA.0b013e318165c075.
10
Is adrenal venous sampling necessary in all patients with hyperaldosteronism before adrenalectomy?对于所有原发性醛固酮增多症患者,在进行肾上腺切除术之前都有必要进行肾上腺静脉采血吗?
J Vasc Interv Radiol. 2008 Jan;19(1):66-71. doi: 10.1016/j.jvir.2007.08.022.