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多囊肾病患者新月体性肾小球肾炎所致急性肾损伤

Acute Kidney Injury due to Crescentic Glomerulonephritis in a Patient with Polycystic Kidney Disease.

作者信息

Maggard Reuben, Makary Raafat, Monteiro Carmela L, James Leighton R

机构信息

Division of Nephrology and Hypertension, Department of Medicine, University of Florida, Jacksonville, Fla., USA.

出版信息

Case Rep Nephrol Urol. 2013 Jul 11;3(2):99-104. doi: 10.1159/000353850. Print 2013 Jul.

DOI:10.1159/000353850
PMID:23914203
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3731623/
Abstract

Polycystic kidney disease is an inherited condition, characterized by the development of cysts in the kidney, as well as in other organs. Patients with polycystic kidney can suffer from the same causes of acute kidney injury as the general population. Nephritic syndrome is an uncommon cause of acute kidney injury in the general population and less common in patients with polycystic kidney disease. We report the second case of crescentic glomerulonephritis, causing acute kidney injury, in a patient with polycystic kidney disease.

摘要

多囊肾病是一种遗传性疾病,其特征是在肾脏以及其他器官中出现囊肿。多囊肾病患者与普通人群一样,可能因相同原因发生急性肾损伤。在普通人群中,肾炎综合征是急性肾损伤的少见病因,在多囊肾病患者中则更为罕见。我们报告了第二例多囊肾病患者发生新月体性肾小球肾炎并导致急性肾损伤的病例。

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本文引用的文献

1
Massive proteinuria and autosomal dominant polycystic kidney disease: a rare coincidence.大量蛋白尿与常染色体显性多囊肾病:一种罕见的巧合。
Iran J Kidney Dis. 2012 Jan;6(1):73-6.
2
Nephrotic syndrome and idiopathic membranous nephropathy associated with autosomal-dominant polycystic kidney disease.肾病综合征及特发性膜性肾病与常染色体显性遗传性多囊肾病相关。
ScientificWorldJournal. 2011 May 5;11:1041-7. doi: 10.1100/tsw.2011.94.
3
Autosomal dominant polycystic kidney disease with diffuse proliferative glomerulonephritis - an unusual association: a case report and review of the literature.常染色体显性多囊肾病合并弥漫性增生性肾小球肾炎——一种不寻常的关联:一例病例报告及文献复习
J Med Case Rep. 2010 Apr 29;4:125. doi: 10.1186/1752-1947-4-125.
4
Renal injury is a third hit promoting rapid development of adult polycystic kidney disease.肾损伤是促使成人多囊肾病快速发展的第三次打击。
Hum Mol Genet. 2009 Jul 15;18(14):2523-31. doi: 10.1093/hmg/ddp147. Epub 2009 Apr 2.
5
Pkd1 inactivation induced in adulthood produces focal cystic disease.成年期诱导的Pkd1失活会产生局灶性囊性疾病。
J Am Soc Nephrol. 2008 Dec;19(12):2351-63. doi: 10.1681/ASN.2007101139. Epub 2008 Sep 5.
6
Polycystic kidney disease.多囊肾病
J Am Soc Nephrol. 2007 May;18(5):1371-3. doi: 10.1681/ASN.2007030299. Epub 2007 Apr 11.
7
Nephrotic syndrome and IgA nephropathy in polycystic kidney disease.多囊肾病中的肾病综合征和IgA肾病
Clin Exp Nephrol. 2006 Jun;10(2):136-9. doi: 10.1007/s10157-005-0403-6.
8
Autosomal dominant polycystic kidney disease (ADPKD, MIM 173900, PKD1 and PKD2 genes, protein products known as polycystin-1 and polycystin-2).常染色体显性多囊肾病(ADPKD,MIM 173900,PKD1和PKD2基因,其蛋白质产物分别称为多囊蛋白-1和多囊蛋白-2)
Eur J Hum Genet. 2004 May;12(5):347-54. doi: 10.1038/sj.ejhg.5201162.
9
Genetics and pathogenesis of polycystic kidney disease.多囊肾病的遗传学与发病机制
J Am Soc Nephrol. 2002 Sep;13(9):2384-98. doi: 10.1097/01.asn.0000028643.17901.42.
10
A "two-hit" model of cystogenesis in autosomal dominant polycystic kidney disease?常染色体显性多囊肾病囊肿形成的“双打击”模型?
Trends Mol Med. 2001 Apr;7(4):151-6. doi: 10.1016/s1471-4914(01)01953-0.