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Rifampicin-Associated Secondary Minimal Change Disease Presenting with Nephrotic Syndrome in a Pulmonary Tuberculosis
Satyanand Sathi1, Anil Kumar Garg1, Manoj Kumar Singh1
1Department of Medicine, S.M.M.H. Government Medical College, Saharanpur, Uttar Pradesh, India.
Abstract:
Various extraglomerular disease processes have been associated with drug-induced secondary minimal change disease (MCD). In a majority of cases, preferably, a hypersensitivity reaction appears to be involved, and in some cases, there is direct toxic effect over glomerular capillaries. There are several reports to demonstrate that rifampicin has been associated with various nephrotoxic adverse effects, but rifampicin-induced secondary minimal change disease (MCD) is very rare. Here, we report the case of a young adult male who presented with nephrotic proteinuria with bland urine sediment after one month of initiation of rifampicin treatment for pulmonary tuberculosis. The patient had no proteinuria before the start of antituberculosis treatment. Renal biopsy showed nonproliferative glomerulopathy and immunofluorescence did not show significant glomerular immune deposits. Electron microscopy showed diffuse effacement of visceral epithelial cell foot processes and did not show any presence of glomerular immune complexes and thickening of glomerular basement membrane, promoting the diagnosis of minimal change nephrotic syndrome. The patient got complete remission after discontinuation of rifampicin.
Insights
Rifampicin, an antibiotic for tuberculosis, can rarely cause secondary minimal change disease (MCD) leading to nephrotic syndrome. Discontinuation of the drug resulted in complete remission, highlighting its potential nephrotoxicity.
Area of Science:
- Nephrology
- Pharmacology
- Pathology
Background:
- Drug-induced secondary minimal change disease (MCD) is often linked to hypersensitivity or direct toxicity.
- Rifampicin is known for various nephrotoxic effects, but MCD induction is exceptionally rare.
Observation:
- A young adult male developed nephrotic proteinuria after one month of rifampicin treatment for tuberculosis.
- The patient had no prior proteinuria, and urine sediment was unremarkable.
Findings:
- Renal biopsy revealed nonproliferative glomerulopathy with effaced foot processes on electron microscopy.
- Immunofluorescence and electron microscopy excluded immune deposits and basement membrane thickening, confirming minimal change nephrotic syndrome.
Implications:
- This case underscores the rare but significant nephrotoxicity of rifampicin, specifically its potential to induce minimal change disease.
- Prompt recognition and drug withdrawal are crucial for managing rifampicin-induced nephrotic syndrome and achieving remission.
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