IgG4-related membranous glomerulonephritis and generalized lymphadenopathy without pancreatitis: a case report

Abstract Background IgG4-related disease is a recently described pathologic entity. This is the case of a patient with nephrotic syndrome and lymphadenopathy due to IgG4-related disease. Such a kidney involvement is quite peculiar and has only been described a few times recently. Renal biopsy showed...

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Main Authors: Justine Huart, Stéphanie Grosch, Christophe Bovy, Michel Moutschen, Jean-Marie Krzesinski
Format: Article
Language:English
Published: BMC 2017-04-01
Series:BMC Nephrology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12882-017-0561-2
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spelling doaj-94232a4af5324ec6ba1d12af577af6292020-11-25T02:34:42ZengBMCBMC Nephrology1471-23692017-04-011811810.1186/s12882-017-0561-2IgG4-related membranous glomerulonephritis and generalized lymphadenopathy without pancreatitis: a case reportJustine Huart0Stéphanie Grosch1Christophe Bovy2Michel Moutschen3Jean-Marie Krzesinski4Division of Nephrology, University of Liège Hospital (ULg CHU)Division of Nephrology, University of Liège Hospital (ULg CHU)Division of Nephrology, University of Liège Hospital (ULg CHU)Division of Infectious diseases and General Internal Medecine, University of Liège Hospital (ULg CHU)Division of Nephrology, University of Liège Hospital (ULg CHU)Abstract Background IgG4-related disease is a recently described pathologic entity. This is the case of a patient with nephrotic syndrome and lymphadenopathy due to IgG4-related disease. Such a kidney involvement is quite peculiar and has only been described a few times recently. Renal biopsy showed a glomerular involvement with membranous glomerulonephritis in association with a tubulo-interstitial nephropathy. Moreover, the patient was not suffering from pancreatitis. Case presentation The patient is a middle-aged man of Moroccan origin. He has developed recurrent episodes of diffuse lymphadenopathies, renal failure and nephrotic syndrome. Renal biopsies showed membranous glomerulonephritis. Discussion and conclusion The diagnostic approach of this atypical presentation is discussed in this case report as well as diagnostic criteria, therapeutic strategies, biomarkers and pathophysiology of IgG4-related disease. IgG4-related membranous glomerulonephritis is a well-established cause of membranous glomerulonephritis. It must be sought after in every patient with a previous diagnosis of IgG4-related disease and in every patient with this histological finding on renal biopsy. Corticoids are still the first-line treatment of IgG4-related disease. New therapeutic strategies are needed to avoid glucocorticoids long term side-effects. Interestingly, the patient was prescribed cyclophosphamide in addition to glucocorticoids for an immune thrombocytopenia. This treatment had a very good impact on his IgG4-related disease.http://link.springer.com/article/10.1186/s12882-017-0561-2IgG4-related diseaseIgG4-related kidney diseaseLymphadenopathyMembranous glomerulonephritisNephrotic syndrome
collection DOAJ
language English
format Article
sources DOAJ
author Justine Huart
Stéphanie Grosch
Christophe Bovy
Michel Moutschen
Jean-Marie Krzesinski
spellingShingle Justine Huart
Stéphanie Grosch
Christophe Bovy
Michel Moutschen
Jean-Marie Krzesinski
IgG4-related membranous glomerulonephritis and generalized lymphadenopathy without pancreatitis: a case report
BMC Nephrology
IgG4-related disease
IgG4-related kidney disease
Lymphadenopathy
Membranous glomerulonephritis
Nephrotic syndrome
author_facet Justine Huart
Stéphanie Grosch
Christophe Bovy
Michel Moutschen
Jean-Marie Krzesinski
author_sort Justine Huart
title IgG4-related membranous glomerulonephritis and generalized lymphadenopathy without pancreatitis: a case report
title_short IgG4-related membranous glomerulonephritis and generalized lymphadenopathy without pancreatitis: a case report
title_full IgG4-related membranous glomerulonephritis and generalized lymphadenopathy without pancreatitis: a case report
title_fullStr IgG4-related membranous glomerulonephritis and generalized lymphadenopathy without pancreatitis: a case report
title_full_unstemmed IgG4-related membranous glomerulonephritis and generalized lymphadenopathy without pancreatitis: a case report
title_sort igg4-related membranous glomerulonephritis and generalized lymphadenopathy without pancreatitis: a case report
publisher BMC
series BMC Nephrology
issn 1471-2369
publishDate 2017-04-01
description Abstract Background IgG4-related disease is a recently described pathologic entity. This is the case of a patient with nephrotic syndrome and lymphadenopathy due to IgG4-related disease. Such a kidney involvement is quite peculiar and has only been described a few times recently. Renal biopsy showed a glomerular involvement with membranous glomerulonephritis in association with a tubulo-interstitial nephropathy. Moreover, the patient was not suffering from pancreatitis. Case presentation The patient is a middle-aged man of Moroccan origin. He has developed recurrent episodes of diffuse lymphadenopathies, renal failure and nephrotic syndrome. Renal biopsies showed membranous glomerulonephritis. Discussion and conclusion The diagnostic approach of this atypical presentation is discussed in this case report as well as diagnostic criteria, therapeutic strategies, biomarkers and pathophysiology of IgG4-related disease. IgG4-related membranous glomerulonephritis is a well-established cause of membranous glomerulonephritis. It must be sought after in every patient with a previous diagnosis of IgG4-related disease and in every patient with this histological finding on renal biopsy. Corticoids are still the first-line treatment of IgG4-related disease. New therapeutic strategies are needed to avoid glucocorticoids long term side-effects. Interestingly, the patient was prescribed cyclophosphamide in addition to glucocorticoids for an immune thrombocytopenia. This treatment had a very good impact on his IgG4-related disease.
topic IgG4-related disease
IgG4-related kidney disease
Lymphadenopathy
Membranous glomerulonephritis
Nephrotic syndrome
url http://link.springer.com/article/10.1186/s12882-017-0561-2
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