ReviewClinical and experimental nephrology2011
Clinicopathological findings of immunoglobulin G4-related kidney disease.
Review in Clinical and experimental nephrology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.
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Who cites it
24 citing papers in PubMed, 64 citations in OpenAlex.
- Article
- Improved Renal Function in Initial Treatment Improves Patient Survival, Renal Outcomes, and Glucocorticoid-Related Complications in IgG4-Related Kidney Disease in Japan.Kidney international reports · 2024Article
- Unique Challenges in Diagnosing IgG4-Related Tubulointerstitial Nephritis with Arteritis.Kansas journal of medicine · 2022Article
- Long-term changes in renal function after treatment initiation and the importance of early diagnosis in maintaining renal function among IgG4-related tubulointerstitial nephritis patients in Japan.Arthritis research & therapy · 2020Article
- Idiopathic membranous nephropathy in a patient diagnosed with IgG4-related disease: A case report.Medicine · 2020Article
- Progression of immunoglobulin G4-related disease to systematic lupus erythematosus after gastric cancer surgery: A case report.Medicine · 2018Article
- An IgA1-lambda-type monoclonal immunoglobulin deposition disease associated with membranous features in a patient with IgG4-related kidney disease: a case report.BMC nephrology · 2018Article
- Clinical features and prognostic factors of ten patients with renal failure caused by IgG4-related retroperitoneal fibrosis.Oncotarget · 2018Article
- Estimation of the number of histological diagnosis for IgG4-related kidney disease referred to the data obtained from the Japan Renal Biopsy Registry (J-RBR) questionnaire and cases reported in the Japanese Society of Nephrology Meetings.Clinical and experimental nephrology · 2017Article
- Factors related to renal cortical atrophy development after glucocorticoid therapy in IgG4-related kidney disease: a retrospective multicenter study.Arthritis research & therapy · 2016Article
- IgG4-related inflammatory pseudotumor of the renal pelvis involving renal parenchyma, mimicking malignancy.Diagnostic pathology · 2016Article
- Overview of IgG4-Related Tubulointerstitial Nephritis and Its Mimickers.Journal of pathology and translational medicine · 2016Review
- Membranoproliferative glomerulonephritis with predominant IgG2 and IgG3 deposition in a patient with IgG4-related disease.BMC nephrology · 2015Article
- Evaluation of diagnostic criteria for IgG4-related tubulointerstitial nephritis.Diagnostic pathology · 2015Article
- An Overlapping Case of Lupus Nephritis and IgG4-Related Kidney Disease.Journal of clinical medicine research · 2015Article
- Tubulointerstitial fibrosis in patients with IgG4-related kidney disease: pathological findings on repeat renal biopsy.Rheumatology international · 2015Article
- IgG4-related tubulointerstitial nephritis associated with only lymphadenopathy and without elevated serum IgG4 or renal imaging abnormalities: a case report and literature review.International journal of clinical and experimental medicine · 2015Article
- Membranous nephropathy associated with type 1 autoimmune pancreatitis and dominant glomerular IgG4 deposit.CEN case reports · 2014Article
- IgG4-related renal disease: clinical and pathological characteristics.International journal of clinical and experimental pathology · 2014Review
- IgG4-Related Tubulointerstitial Nephritis Associated with Membranous Nephropathy in Two Patients: Remission after Administering a Combination of Steroid and Mizoribine.Case reports in nephrology · 2014Article
Corrections and comments
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Authors and funding
5 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Immunoglobulin (Ig) G4-related kidney disease characterizing tubulointerstitial nephritis (TIN) is an organ complication recognized in IgG4-related systemic diseases that has some unique aspects compared to other types of TIN. TIN lesions in the kidney can be tumor-like, focal or diffuse. Abnormal urinalysis is usually mild or absent even in the cases with deteriorated renal dysfunction. Some cases are accidentally diagnosed from radiological findings without renal dysfunction and/or abnormal urinalysis. The typical pathological findings of TIN are unique fibrosis and infiltration of massive lymphocytes and IgG4-positive plasma cells. Glomerular lesions are rare but the complication of mesangial proliferative glomerulonephritis and membranous nephropathy is occasionally reported. Pathogenic mechanisms are unclear until now; however, auto-immune and allergic mechanisms have been suspected from laboratory data. The initial response to steroid agents is generally favorable; however, recurrence is possible after the discontinuation of steroid treatment. Long-term follow-up is necessary with continuous systemic checks for organ disorders due to IgG4-related systemic diseases.
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