Schistosoma mansoni associated glomerulopathy with IgA mesangial deposits: case report

Abstract Introduction: Renal involvement is a severe form of schistosomiasis and occurs in 10% to 15% of patients with the hepatosplenic form of the disease. Nephrotic syndrome is the most common clinical presentation. It is a complication caused by immune complexes (IC), it is rare to appear in th...

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Main Authors: Fabiana Oliveira Gonçalves, Tânia Maria de Souza Fontes, Ana Paula Pereira Santana Lemes Canuto
Format: Article
Language:English
Published: Sociedade Brasileira de Nefrologia
Series:Brazilian Journal of Nephrology
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002017000100086&lng=en&tlng=en
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spelling doaj-3f22984d187a4758bec5d7862c3aca062020-11-25T02:26:02ZengSociedade Brasileira de NefrologiaBrazilian Journal of Nephrology2175-8239391869010.5935/0101-2800.20170015S0101-28002017000100086Schistosoma mansoni associated glomerulopathy with IgA mesangial deposits: case reportFabiana Oliveira GonçalvesTânia Maria de Souza FontesAna Paula Pereira Santana Lemes CanutoAbstract Introduction: Renal involvement is a severe form of schistosomiasis and occurs in 10% to 15% of patients with the hepatosplenic form of the disease. Nephrotic syndrome is the most common clinical presentation. It is a complication caused by immune complexes (IC), it is rare to appear in the Brazilian context with a immunoglobulin A (IgA) deposits. When installed the renal injury by Schistosoma mansoni, classically presents as membranoproliferative glomerulonephritis (mesangiocapillary) with lobular accentuation. Objective: To report a case of schistosomiasis nephropathy that appeared 7 years after treatment of hepatosplenic schistosomiasis with histologic pattern of mesangial proliferative glomerulonephritis with IgA deposits in mesangium. Clinically developed with progressive decrease of proteinuria with angiotensin receptor blocker (ARB). Method: It was reported a case of a 36 years old patient, brown, with classical sintoms of nephrotic syndrome (proteinuria > 3.5 g/24h, hypoalbuminemia and hypercholesterolemia), however with hepatosplenic schistosomiasis history 7 years ago and portal hypertension. Patient underwent renal biopsy which showed IgA deposits in mesangial, being more intense than immunoglobulin G (IgG), accompanied by C1q and C3, with 4/13 glomeruli sclerotic, standard light mesangial glomerulonephritis renal injury with IgA deposits. Patient began taking ARB with progressive improvement in proteinuria. Conclusion: Patients with glomerulonephritis by schistosoma don't show improvement of disease progression with antiparasitic treatment. However the anti-proteinuric treatment can slow the progression of end stage kidney disease.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002017000100086&lng=en&tlng=enangiotensin receptor antagonistsglomerulonephritis, IGASchistosoma mansoni
collection DOAJ
language English
format Article
sources DOAJ
author Fabiana Oliveira Gonçalves
Tânia Maria de Souza Fontes
Ana Paula Pereira Santana Lemes Canuto
spellingShingle Fabiana Oliveira Gonçalves
Tânia Maria de Souza Fontes
Ana Paula Pereira Santana Lemes Canuto
Schistosoma mansoni associated glomerulopathy with IgA mesangial deposits: case report
Brazilian Journal of Nephrology
angiotensin receptor antagonists
glomerulonephritis, IGA
Schistosoma mansoni
author_facet Fabiana Oliveira Gonçalves
Tânia Maria de Souza Fontes
Ana Paula Pereira Santana Lemes Canuto
author_sort Fabiana Oliveira Gonçalves
title Schistosoma mansoni associated glomerulopathy with IgA mesangial deposits: case report
title_short Schistosoma mansoni associated glomerulopathy with IgA mesangial deposits: case report
title_full Schistosoma mansoni associated glomerulopathy with IgA mesangial deposits: case report
title_fullStr Schistosoma mansoni associated glomerulopathy with IgA mesangial deposits: case report
title_full_unstemmed Schistosoma mansoni associated glomerulopathy with IgA mesangial deposits: case report
title_sort schistosoma mansoni associated glomerulopathy with iga mesangial deposits: case report
publisher Sociedade Brasileira de Nefrologia
series Brazilian Journal of Nephrology
issn 2175-8239
description Abstract Introduction: Renal involvement is a severe form of schistosomiasis and occurs in 10% to 15% of patients with the hepatosplenic form of the disease. Nephrotic syndrome is the most common clinical presentation. It is a complication caused by immune complexes (IC), it is rare to appear in the Brazilian context with a immunoglobulin A (IgA) deposits. When installed the renal injury by Schistosoma mansoni, classically presents as membranoproliferative glomerulonephritis (mesangiocapillary) with lobular accentuation. Objective: To report a case of schistosomiasis nephropathy that appeared 7 years after treatment of hepatosplenic schistosomiasis with histologic pattern of mesangial proliferative glomerulonephritis with IgA deposits in mesangium. Clinically developed with progressive decrease of proteinuria with angiotensin receptor blocker (ARB). Method: It was reported a case of a 36 years old patient, brown, with classical sintoms of nephrotic syndrome (proteinuria > 3.5 g/24h, hypoalbuminemia and hypercholesterolemia), however with hepatosplenic schistosomiasis history 7 years ago and portal hypertension. Patient underwent renal biopsy which showed IgA deposits in mesangial, being more intense than immunoglobulin G (IgG), accompanied by C1q and C3, with 4/13 glomeruli sclerotic, standard light mesangial glomerulonephritis renal injury with IgA deposits. Patient began taking ARB with progressive improvement in proteinuria. Conclusion: Patients with glomerulonephritis by schistosoma don't show improvement of disease progression with antiparasitic treatment. However the anti-proteinuric treatment can slow the progression of end stage kidney disease.
topic angiotensin receptor antagonists
glomerulonephritis, IGA
Schistosoma mansoni
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002017000100086&lng=en&tlng=en
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