Related Experiment Video
Updated: Oct 26, 2025

An Immunohistopathologic Study to Profile the Folate Receptor Beta Macrophage and Vascular Immune Microenvironment in Giant Cell Arteritis
Published on: February 8, 2019
IgG4 tubulointerstitial nephritis - An uncommon enemy!
Kavita Jain1, Moumita Sengupta1, Keya Basu1
1Department of Pathology, IPGME and R and SSKM Hospital, Kolkata, West Bengal, India.
This case report highlights IgG4-related kidney disease (IgG4-RKD), specifically IgG4-related tubulointerstitial nephritis (IgG4-TIN), presenting as unexplained renal dysfunction. Early recognition is crucial to prevent misdiagnosis of this rare IgG4-RD manifestation.
Area of Science:
- Nephrology
- Immunology
- Pathology
Background:
- IgG4-related disease (IgG4-RD) is an immune-mediated condition causing fibroinflammatory lesions in multiple organs.
- IgG4-related kidney disease (IgG4-RKD) is a rare manifestation, often involving glomerular or extraglomerular compartments.
- Accurate diagnosis of IgG4-RKD is challenging, necessitating increased awareness to avoid misdiagnosis.
More Related Videos
Related Concept Videos
Acute Kidney Injury II: Pathophysiology
Acute Pyelonephritis I: Introduction
Chronic Kidney Disease III: Interprofessional Care
Nephrotic Syndrome I : Introduction
Acute Pyelonephritis II: Diagnostic Studies and Management
Acute Kidney Injury IV: Diagnostic Studies and Prevention

