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脱氧皮质酮分泌瘤作为难治性高血压的一个病因

Deoxycorticosterone producing tumor as a cause of resistant hypertension.

作者信息

Gupta Saurabh, Melendez Jose, Khanna Apurv

机构信息

University of Connecticut Health Center, Farmington, CT 06030, USA.

出版信息

Case Rep Med. 2010;2010:372719. doi: 10.1155/2010/372719. Epub 2010 Jun 30.

Abstract

We describe a young woman with longstanding resistant hypertension. Evaluation for renal artery stenosis and primary aldosteronism was unrevealing. In this setting of a suppressed plasma aldosterone concentration (PAC) and a suppressed plasma renin activity (PRA), a differential diagnosis of a deoxycorticosterone (DOC) producing tumor was entertained. Biochemical and imaging studies confirmed this diagnosis. Rare and novel DOC producing tumors are an important cause of resistant hypertension.

摘要

我们描述了一位患有长期顽固性高血压的年轻女性。对肾动脉狭窄和原发性醛固酮增多症的评估未发现异常。在血浆醛固酮浓度(PAC)和血浆肾素活性(PRA)均受抑制的情况下,考虑了脱氧皮质酮(DOC)分泌瘤的鉴别诊断。生化和影像学研究证实了这一诊断。罕见且新颖的DOC分泌瘤是顽固性高血压的重要原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d53e/2909735/d5e7b707694e/CRM2010-372719.001.jpg

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