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Erschienen in: International Urology and Nephrology 2/2017

28.10.2016 | Nephrology - Original Paper

Characteristics of patients diagnosed with renal vein thrombosis and glomerulopathy: a case series

verfasst von: Oliver Ross, Andrew Pourmoussa, Michael Batech, John J. Sim

Erschienen in: International Urology and Nephrology | Ausgabe 2/2017

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Abstract

Background

Few contemporary studies have evaluated the clinical characteristics of patients with biopsy-proven glomerulopathy diagnosed with renal vein thrombosis (RVT).

Methods

Retrospective case series study within an integrated health system in a 12-year period (January 1, 2000 through December 31, 2011) investigating clinical characteristics of all adult patients who underwent native or transplant kidney biopsy and also had a diagnosis of RVT. Patient characteristics, diagnostic studies, and outcomes were evaluated.

Results

Among 3763 eligible patients, 17 had imaging confirmed RVT. Of these, 15 had membranous nephropathy (idiopathic or secondary to autoimmune disease). Although the biopsy population included primary and secondary glomerular disease patients, all 17 RVT patients had severe nephrotic syndrome and profound hypoalbuminemia with mean (SD) of albumin: 1.5 g/dL (0.66).

Conclusion

Clinically significant RVT in patients with glomerulopathy appears to be a rather rare entity, occurring predominantly in patients with severe nephrotic syndrome due to idiopathic membranous nephropathy and membranous nephropathy secondary to autoimmune disease.
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Metadaten
Titel
Characteristics of patients diagnosed with renal vein thrombosis and glomerulopathy: a case series
verfasst von
Oliver Ross
Andrew Pourmoussa
Michael Batech
John J. Sim
Publikationsdatum
28.10.2016
Verlag
Springer Netherlands
Erschienen in
International Urology and Nephrology / Ausgabe 2/2017
Print ISSN: 0301-1623
Elektronische ISSN: 1573-2584
DOI
https://doi.org/10.1007/s11255-016-1442-5

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