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[Membranous nephropathy].

Authors:
Elsa Martin Passos Bruno Legallicier Michel Godin

Rev Prat 2003 Nov;53(18):2033-8

Service de néphrologie, hôpital de Bois-Guillaume, CHU Rouen, 76031 Rouen Cedex.

Membranous nephropathy is the most common cause of idiopathic nephrotic syndrome in adults. The frequency of secondary forms varies from 20 to 30 per cent. The principal causes appear to be systemic lupus erythematosous, drug therapy, malignancy and viral infection. The pathology includes normocellular glomeruli with subepithelial deposits on the outer surface of the glomerular basement membrane. Immunofluorescence studies reveal consistently IgG granular deposits. Prolonged high-grade proteinuria is common. Renal vein thrombosis is frequently associated. Persistent hyperlipidemia increases the risk of cardiovascular diseases. The course of idiopathic membranous nephropathy remains variable. Numerous factors affecting the prognosis of the nephropathy have been identified and should be considered for the decision of specific treatment and use of immunosuppressive therapy.

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November 2003

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Recurrent membranous nephropathy after transplantation: donor antigen and HLA converge in defining risk.

Authors:
Kate J Robson A Richard Kitching

Kidney Int 2021 Mar;99(3):545-548

Centre for Inflammatory Diseases, Monash University Department of Medicine, Monash Medical Centre, Monash University, Clayton, Victoria, Australia; Department of Nephrology, Monash Health, Clayton, Victoria, Australia; Department of Pediatric Nephrology, Monash Health, Clayton, Victoria, Australia. Electronic address:

Membranous nephropathy, like many forms of glomerulonephritis, is an HLA-associated autoimmune disease that can recur in the transplanted kidney. In this issue of Kidney International, Berchtold and colleagues publish an intriguing and important paper on risk factors for recurrent post-transplant membranous nephropathy due to autoimmunity to PLA2R1. They found that the genetics of both the autoantigen and donor HLA are important determinants of the risk of recurrent disease in the graft. Read More

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March 2021
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Membranous nephropathy in a patient with coronavirus disease 2019 (COVID-19): A case report.

Authors:
Jing Miao Mary E Fidler Samih H Nasr Christopher P Larsen Ziad M Zoghby

Clin Nephrol Case Stud 2021 19;9:11-18. Epub 2021 Feb 19.

Division of Nephrology and Hypertension.

Introduction: Though respiratory, immune, and coagulation systems are major targets of coronavirus disease 2019 (COVID-19), kidney dysfunction, presenting with acute kidney injury (AKI), is also common. Most AKI cases in COVID-19 manifest as acute tubular injury (ATI) in conjunction with multiorgan failure. While initial renal pathological findings were limited to acute tubular necrosis and collapsing glomerulopathy, a recent case series reported a larger spectrum of findings. Read More

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February 2021
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Comparison of Ultrastructural Features Between Patients with Mercury-associated Membranous Nephropathy and Idiopathic Membranous Nephropathy.

Authors:
Ai-Bo Qin Zi-Shan Lin Su-Xia Wang Hui Wang Zhao Cui Fu-de Zhou Ming-Hui Zhao

Am J Med Sci 2020 Nov 26. Epub 2020 Nov 26.

Renal Division, Department of Medicine, Peking University First Hospital, Renal Pathology Center, Institute of Nephrology, Peking University, Key Laboratory of Renal Disease, Ministry of Health of China, Key Laboratory of CKD Prevention and Treatment, Ministry of Education of China, Research Units of Diagnosis and Treatment of Immune-mediated Kidney Diseases, Chinese Academy of Medical Sciences, Beijing, China; Peking-Tsinghua Center for Life Sciences, Beijing, China.

Background: Prolonged exposure to mercury can cause membranous nephropathy. Mercury-associated membranous nephropathy (M-MN) and idiopathic membranous nephropathy (I-MN) have similar clinical manifestations, making misdiagnoses likely. We compared the clinicopathological and ultrastructural features of M-MN and I-MN. Read More

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November 2020
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IgG4-related kidney disease with systemic Epstein-Barr virus infection: A case report.

Authors:
Yan Zhong W Dean Wallace Annika Khine Chandnish Ahluwalia Miroslaw J Smogorzewski

Clin Nephrol 2021 Feb 24. Epub 2021 Feb 24.

IgG4-related disease (IgG4-RD) is a newly recognized multi-organ fibro-inflammatory condition with characteristic histopathological findings of increased IgG4+ plasma cells in tissue and usually with increased IgG4 serum levels. Kidney involvement in IgG4-RD has been well described since 2006. Epstein-Barr virus (EBV) has reportedly been associated with nodal IgG4-RD, but not in extra-nodal disease. Read More

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February 2021
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Spectrum of Kidney Diseases in Patients With Hepatitis C Virus Infection.

Authors:
Shunhua Guo Meghan E Kapp Diego M Beltran Cesar Y Cardona Dawn J Caster Ronald R Reichel Agnes B Fogo

Am J Clin Pathol 2021 Feb 24. Epub 2021 Feb 24.

Department of Pathology, Microbiology and Immunology, Vanderbilt University School of Medicine, Nashville, TN, USA.

Objectives: To study the pathologic spectrum of kidney diseases in patients with hepatitis C virus infection (HCV+).

Methods: Native kidney biopsy specimens in HCV+ patients were reviewed.

Results: A total of 9,836 native kidney biopsy specimens were evaluated from January 2007 to December 2016, of which 273 (2. Read More

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February 2021
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