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页肾:继发性高血压的罕见病因。

Page kidney: A rare cause of secondary hypertension.

作者信息

Warnich Ilonka, Nicolaou Mark, Sofianos Zelia, Pienaar Jacobus A, Varghese Jacob

机构信息

Department of Diagnostic Radiology, University of the Witwatersrand, Johannesburg, South Africa.

Department of Diagnostic Radiology, Klerksdorp/Tshepong Hospital Complex, Klerksdorp, South Africa.

出版信息

SA J Radiol. 2019 Sep 23;23(1):1762. doi: 10.4102/sajr.v23i1.1762. eCollection 2019.

DOI:10.4102/sajr.v23i1.1762
PMID:31754544
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6837813/
Abstract

Page kidney is a rare phenomenon that can present with hypertension. The presence of a subcapsular perirenal collection causes parenchymal compression leading to renal hypoperfusion. Subsequent activation of the renin-angiotensin-aldosterone system results in an increase in systemic blood pressure. The causes of renal subcapsular collections are varied, with most cases being secondary to post-traumatic haematomas. We present the case of a young hypertensive patient, treated as primary hypertension with persistently uncontrolled blood pressures. This was despite good treatment adherence. On further investigation, imaging identified the presence of bilateral subcapsular collections. This case illustrates the importance of a thorough workup in a young hypertensive patient with refractory hypertension. Given that Page kidney is curable, timeous intervention can save the patient from unnecessary medications and the morbidity of uncontrolled blood pressures.

摘要

佩奇肾是一种罕见的现象,可伴有高血压。肾周包膜下积液的存在会导致实质受压,进而引起肾灌注不足。随后肾素-血管紧张素-醛固酮系统的激活会导致全身血压升高。肾包膜下积液的病因多种多样,大多数病例继发于创伤后血肿。我们报告一例年轻高血压患者的病例,该患者被当作原发性高血压治疗,但血压持续控制不佳。尽管患者对治疗依从性良好,但仍出现这种情况。进一步检查时,影像学检查发现双侧包膜下积液。该病例说明了对难治性高血压的年轻患者进行全面检查的重要性。鉴于佩奇肾是可治愈的,及时干预可使患者避免不必要的药物治疗以及血压控制不佳带来的不良影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edf6/6837813/9ccea7fb81d7/SAJR-23-1762-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edf6/6837813/58744ffc9282/SAJR-23-1762-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edf6/6837813/e90c880f8b63/SAJR-23-1762-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edf6/6837813/9ccea7fb81d7/SAJR-23-1762-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edf6/6837813/58744ffc9282/SAJR-23-1762-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edf6/6837813/e90c880f8b63/SAJR-23-1762-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edf6/6837813/9ccea7fb81d7/SAJR-23-1762-g003.jpg

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引用本文的文献

1
A Rare Case of Intravenously Managed Hypertensive Emergency Arising from a Perirenal Hematoma Subsequent to a Native Kidney Biopsy.一例因自体肾活检后肾周血肿引发的静脉给药治疗的高血压急症罕见病例。
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2
Bilateral Page kidney in a postpartum female: a case report.产后女性双侧盘状肾:一例报告
Ann Med Surg (Lond). 2023 Feb 7;85(2):225-227. doi: 10.1097/MS9.0000000000000196. eCollection 2023 Feb.

本文引用的文献

1
Page kidney: A rare but surgically treatable cause of hypertension.页肾:一种罕见但可通过手术治疗的高血压病因。
Saudi J Kidney Dis Transpl. 2018 Jan-Feb;29(1):193-197. doi: 10.4103/1319-2442.225183.
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Bilateral nontraumatic recurrent Page kidney.双侧非创伤性复发性佩奇肾。
Radiol Case Rep. 2017 Jun 17;12(3):511-513. doi: 10.1016/j.radcr.2017.05.003. eCollection 2017 Sep.
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Renal lymphangiectasia treated with percutaneous drainage and sclerotherapy.经皮引流及硬化治疗肾淋巴管扩张症。
Int J Adolesc Med Health. 2017 Jun 9;31(4):ijamh-2017-0024. doi: 10.1515/ijamh-2017-0024.
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Recurrent spontaneous renal haemorrhage due to polyarteritis nodosa: a medical cause for a surgical problem.结节性多动脉炎所致复发性自发性肾出血:一个外科问题的医学病因
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An approach to the young hypertensive patient.年轻高血压患者的治疗方法。
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Acute renal failure and arterial hypertension due to subcapsular haematoma: is percutaneous drainage a feasible treatment?肾包膜下血肿所致急性肾衰竭和动脉高血压:经皮引流是否为可行的治疗方法?
BMJ Case Rep. 2016 Jan 18;2016:bcr2015212769. doi: 10.1136/bcr-2015-212769.
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Page kidney: etiology, renal function outcomes and risk for future hypertension.分页肾:病因、肾功能结局和未来高血压风险。
J Clin Hypertens (Greenwich). 2012 Apr;14(4):216-21. doi: 10.1111/j.1751-7176.2012.00601.x. Epub 2012 Mar 12.
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Page kidney as a rare cause of hypertension: case report and review of the literature.盘状肾作为高血压的罕见病因:病例报告及文献复习
Am J Kidney Dis. 2009 Aug;54(2):334-9. doi: 10.1053/j.ajkd.2008.11.014. Epub 2009 Jan 23.
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BJU Int. 2006 Nov;98(5):943-4. doi: 10.1111/j.1464-410X.2006.06432.x.