Crescentic Glomerulonephritis Associated with Polycythaemia Vera: A Rare Occurrence
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Updated: Sep 22, 2025

Glomerular Outgrowth as an Ex Vivo Assay to Analyze Pathways Involved in Parietal Epithelial Cell Activation
Published on: August 19, 2020
Rohan Dwivedi1, K B Shashikiran1, Sonu Manuel1
1Department of Nephrology, Nizams Institute of Medical Sciences, Hyderabad, Telangana, India.
Insights
This case study details a rare instance of crescentic glomerulonephritis (CrGN) in a patient with polycythaemia vera (PV). It highlights an unusual immunologically-mediated renal complication of PV.
Area of Science:
- Nephrology
- Hematology
- Internal Medicine
Background:
- Glomerular diseases pose diagnostic and management challenges, particularly when linked to systemic conditions like malignancies.
- Polycythaemia vera (PV) is a myeloproliferative neoplasm characterized by excessive red blood cell production.
Observation:
- A 50-year-old female presented with edema, splenomegaly, renal dysfunction, and severe proteinuria.
- Diagnostic workup revealed coexisting polycythaemia vera (PV) and crescentic glomerulonephritis (CrGN).
Findings:
- Renal involvement in PV is uncommon and typically attributed to hyperviscosity or hypervolemia.
- This case presents a unique instance of PV-associated CrGN, suggesting an immunologically-mediated mechanism rather than hemodynamic effects.
Implications:
- This case expands the understanding of potential renal manifestations in polycythaemia vera.
- It underscores the importance of investigating immunologic pathways in PV-related kidney disease.
- Further research may elucidate the specific mechanisms driving this rare association.
Abstract:
Glomerular diseases are one of the most challenging entities in terms of diagnosis and management, especially when associated with systemic illnesses such as malignant disorders. Herein, a case of crescentic glomerulonephritis (CrGN) associated with polycythaemia vera (PV) in a 50-year-old female is described. She presented with bilateral pedal oedema, splenomegaly, renal dysfunction and severe proteinuria. On evaluation, we found PV and CrGN. Renal involvement in PV is rare and generally considered as a manifestation of hypervolemia or high-viscosity-induced renal hyper-perfusion and hyper-filtration. This is a unique case of immunologically-mediated renal disease in PV.
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