Related Experiment Video
Updated: May 12, 2026

Mechanism of Kemeng Fang's Inhibition of Podocyte Apoptosis in Rats with Membranous Nephropathy through the PI3K/AKT Signaling Pathway
Published on: August 23, 2024
Crescentic glomerulonephritis developing in the course of idiopathic membranoproliferative glomerulonephritis
Alok Sharma1, Ruchika Gupta, Charanjit Lal
1Department of Pathology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India.
Abstract:
Membranoproliferative glomerulonephritis (MPGN) is a rare cause of the nephrotic syndrome in adults and children. Though small focal crescents may be seen in up to 10% of cases of MPGN, the presence of more than 50% crescents (crescentic MPGN) is rare. Very few cases of crescentic transformation of MPGN, documented by subsequent renal biopsies, have been described in the literature. A young female patient underwent kidney biopsy for the nephrotic-nephritic syndrome and was diagnosed as idiopathic MPGN. She was administered immunosuppressive therapy (steroids and cyclophosphamide), with which her renal functions stabilized. Six months later, she presented with features suggestive of rapidly progressive renal failure and underwent a second renal biopsy. The second biopsy showed crescentic glomerulonephritis with immune complex deposition, suggestive of MPGN. A final diagnosis of crescentic transformation of MPGN was made. Crescentic transformation of MPGN is a rare occurrence, but needs to be considered in a patient diagnosed as MPGN and presenting with rapidly progressive renal failure. The cause of such transformation remains to be elucidated.
Insights
Membranoproliferative glomerulonephritis (MPGN) can rarely transform into a crescentic form, leading to rapid kidney failure. This case highlights the importance of considering this rare transformation in MPGN patients with worsening renal function.
Area of Science:
- Nephrology
- Pathology
Background:
- Membranoproliferative glomerulonephritis (MPGN) is a rare nephrotic syndrome cause.
- Crescentic MPGN, defined by >50% crescents, is exceptionally rare.
Observation:
- A young female with idiopathic MPGN initially responded to immunosuppression.
- Six months later, she developed rapidly progressive renal failure.
Findings:
- A second biopsy revealed crescentic glomerulonephritis with immune deposits, confirming MPGN transformation.
- This rare event underscores the potential for MPGN to evolve into a severe crescentic form.
Implications:
- Crescentic transformation of MPGN must be considered in MPGN patients with acute renal failure.
- Further research is needed to understand the mechanisms driving this rare transformation.
More Related Videos
Related Concept Videos
Nephrotic Syndrome I : Introduction
Acute Pyelonephritis I: Introduction
Diabetic Nephropathy
Renal Corpuscle
Glomerulus: Structure and Function
The glomerulus is a tiny, intricate network of capillaries located at the beginning of the nephron. It's enveloped by the Bowman's capsule and receives its blood supply from an afferent arteriole, which divides into numerous capillaries...
Acute Kidney Injury II: Pathophysiology
Nephrons

