ArticleExperimental and therapeutic medicine2015
Polycythemia vera associated with IgA nephropathy: A case report and literature review.
Article in Experimental and therapeutic medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 12 citations in OpenAlex.
- JAK Inhibitor-Induced Improvement of IgA Nephropathy in a Patient With Polycythemia Vera: A Case Report.Kidney medicine · 2026Article
- A case report and literature review of IgA nephropathy presenting as nephrotic syndrome in polycythemia vera.CEN case reports · 2024Review
- Essential thrombocythemia associated with fibrosis involving bilateral renal sinuses: A case report.Radiology case reports · 2023Article
- Minimal change disease caused by polycythemia vera: A case report.World journal of clinical cases · 2022Article
- A Case of Essential Thrombocythemia and IgA Nephropathy with Literature Review of the Concurrence.Case reports in oncological medicine · 2019Article
- Idiopathic erythrocytosis in IgA nephropathy.Indian journal of nephrologyArticle
- Crescentic Glomerulonephritis Associated with Polycythaemia Vera: A Rare Occurrence.Indian journal of nephrologyArticle
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Authors and funding
5 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
A case of polycythemia vera (PV) associated with immunoglobulin A nephropathy (IgAN) in a 57-year-old man is described. The patient had a mild enlargement of the kidneys and elevated serum creatinine level, whereas the glomerular filtration rate was normal. Pathological observation under a light microscope showed mild mesangial hyperplasia. The urinary protein level was found to be positively correlated with changes in blood cell counts. After controlling blood pressure, anti-platelet, hydroxyurea treatment, the patient's proteinuria decreased and renal function remained in the normal range. PV associated with renal disease is rare and generally considered to be associated with hypervolemia or high-viscosity-induced renal hyperperfusion and hyperfiltration. This is a rare case of PV associated with IgAN without a high filtration rate. A review of the clinical features of PV associated with renal disease from previous literature was also conducted. The histological results of the cases varied and included IgAN, focal segmental glomerulosclerosis and membranoproliferative glomerulonephritis.
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