Javascript must be enabled to continue!
PLA2R-positive membranous nephropathy in IgG4-related disease
View through CrossRef
Abstract
Background
IgG4-related disease (IgG4-RD) is a fibroinflammatory disease that affects multiple organs, including the pancreas, lacrimal glands, salivary glands, periaortic/retroperitoneum, and kidney. Interstitial nephritis is a typical renal disorder associated with IgG4-RD, but membranous nephropathy is also seen in some cases.
Case presentation
Herein we report on the case of a 77-year-old male patient with nephrotic syndrome and IgG4-related lung disease. His serum phospholipase A2 receptor (PLA2R) antibody was positive. His renal biopsy specimen was also positive for PLA2R.
The renal biopsy specimen showed membranous nephropathy with equal IgG3 and IgG4 immunofluorescence staining and no interstitial nephritis, suggesting IgG4-RD manifesting as membranous nephropathy.
Conclusions
Nephrotic syndrome caused by membranous nephropathy is sometimes associated with IgG4-RD. In such cases, even if serum PLA2R antibody is positive, it should be considered that the membranous nephropathy may be secondary to IgG4-RD.
Springer Science and Business Media LLC
Title: PLA2R-positive membranous nephropathy in IgG4-related disease
Description:
Abstract
Background
IgG4-related disease (IgG4-RD) is a fibroinflammatory disease that affects multiple organs, including the pancreas, lacrimal glands, salivary glands, periaortic/retroperitoneum, and kidney.
Interstitial nephritis is a typical renal disorder associated with IgG4-RD, but membranous nephropathy is also seen in some cases.
Case presentation
Herein we report on the case of a 77-year-old male patient with nephrotic syndrome and IgG4-related lung disease.
His serum phospholipase A2 receptor (PLA2R) antibody was positive.
His renal biopsy specimen was also positive for PLA2R.
The renal biopsy specimen showed membranous nephropathy with equal IgG3 and IgG4 immunofluorescence staining and no interstitial nephritis, suggesting IgG4-RD manifesting as membranous nephropathy.
Conclusions
Nephrotic syndrome caused by membranous nephropathy is sometimes associated with IgG4-RD.
In such cases, even if serum PLA2R antibody is positive, it should be considered that the membranous nephropathy may be secondary to IgG4-RD.
Related Results
The correlation between PLA2R-Ab levels and clinical characteristics of primary membranous nephropathy, and the exploration of its application value in treatment selection
The correlation between PLA2R-Ab levels and clinical characteristics of primary membranous nephropathy, and the exploration of its application value in treatment selection
Abstract
OBJECTIVE:To analyze differences in clinicopathological features of primary membranous nephropathy (PMN) patients based on PLA2R-Ab titers and assess treatment eff...
Disordered balance of T cell subsets in arterial tertiary lymphoid organs in immunoglobulin G4-related vascular disease
Disordered balance of T cell subsets in arterial tertiary lymphoid organs in immunoglobulin G4-related vascular disease
Abstract
Background
Arterial tertiary lymphoid organs (ATLOs) are ectopic lymphoid structures that control local arterial immun...
Clinical Outcomes After Endovascular Repair and Open Surgery to Treat Immunoglobulin G4–Related and Nonrelated Inflammatory Abdominal Aortic Aneurysms
Clinical Outcomes After Endovascular Repair and Open Surgery to Treat Immunoglobulin G4–Related and Nonrelated Inflammatory Abdominal Aortic Aneurysms
Purpose: To compare the follow-up results of endovascular aneurysm repair (EVAR) vs open surgery (OS) for inflammatory abdominal aortic aneurysms (IAAAs) with regard to immunoglobu...
Mixed-type Castleman Disease Can Mimic IgG4-Related Disease
Mixed-type Castleman Disease Can Mimic IgG4-Related Disease
Immunoglobulin G4 (IgG4)-related disease is an autoimmune disease with increased serum IgG4 concentrations (≥135 mg/dL). Histopathologic examination shows marked plasmacyte infiltr...
P1832IGG4 RELATED DISEASE: NEPHROPATHY AND BONE MARROW FAILURE IN A 2 YEAR-OLD CHILD
P1832IGG4 RELATED DISEASE: NEPHROPATHY AND BONE MARROW FAILURE IN A 2 YEAR-OLD CHILD
Abstract
Background and Aims
IgG4 related disease (IgG4 RD) is a recently recognized systemic immune-mediated disorder. Pathophy...
Clinical immunology<br>Serum trypsin and TCR as novel markers for predicting disease activity in IgG4-related disease
Clinical immunology<br>Serum trypsin and TCR as novel markers for predicting disease activity in IgG4-related disease
<b>Background: </b>IgG4-related disease (IgG4-RD) is a novel disease named in recent years. Because of its varied clinical manifestations, like tumor but not tumor, it ...
Prognostic implication of IgG4 and IgG1-positive cell infiltration in the lung in patients with idiopathic interstitial pneumonia
Prognostic implication of IgG4 and IgG1-positive cell infiltration in the lung in patients with idiopathic interstitial pneumonia
AbstractImmunoglobulin (Ig) G4-positive cells are rarely observed in the lungs of patients with idiopathic interstitial pneumonias (IIPs). IgG1 may be more pathogenic than IgG4, wi...
Immunoglobulin IgG4 and autoimmune hepatitis
Immunoglobulin IgG4 and autoimmune hepatitis
Introduction:
IgG4 disease has been characterised by lymphoplasmacytic inflammation, rich in IgG4 plasma cells, elevated serum IgG4 and clinical improvement with steroi...

