Treatment for Fairness Cream Induced Nephrotic Syndrome
The treatment for fairness cream induced nephrotic syndrome should include immediate discontinuation of the mercury-containing cream, followed by high-dose glucocorticoids for 8-12 weeks, with consideration of chelation therapy with sodium dimercaptosulfonate in cases of confirmed mercury toxicity. 1, 2
Initial Management
- Discontinue all fairness creams immediately as they may contain mercury which is the causative agent for the nephrotic syndrome 1, 2
- Obtain blood and urine mercury levels to confirm mercury toxicity and establish baseline values for monitoring 1, 3
- Perform a kidney biopsy to determine the histological pattern, which is typically minimal change disease or membranous nephropathy in fairness cream induced nephrotic syndrome 1, 3, 2
- Start high-dose glucocorticoids (prednisone or prednisolone) at 1 mg/kg/day (maximum 80 mg) for initial treatment 4, 5
Specific Treatment Based on Histological Findings
For Minimal Change Disease (MCD)
- Administer high-dose glucocorticoids for a total of 8-12 weeks instead of the previously recommended 24 weeks (Grade 1B) 4
- Continue high-dose glucocorticoids until complete remission is achieved, then taper slowly over 6 months 4
- For steroid-resistant cases, consider calcineurin inhibitors (CNIs) as second-line therapy:
For Membranous Nephropathy (MN)
- For NELL-1 positive membranous nephropathy (common in mercury-induced cases), consider modified Ponticelli regimen 3
- If there is no response to glucocorticoids after 4-6 months, initiate calcineurin inhibitors for at least 6 months 4
Chelation Therapy
- For confirmed mercury toxicity, administer sodium dimercaptosulfonate as chelation therapy alongside immunosuppressive treatment 1
- Continue chelation until blood and urinary mercury levels return to normal range 1, 2
Supportive Care
- Implement fluid and sodium restriction to manage edema 6
- Administer diuretics (loop diuretics preferred) for edema control 6, 7
- Start angiotensin-converting enzyme inhibitors (ACEIs) or angiotensin receptor blockers (ARBs) to reduce proteinuria 6, 7
- Monitor for potential complications such as venous thromboembolism, infections, and hyperlipidemia 6
Monitoring and Follow-up
- Regularly monitor proteinuria, serum albumin, renal function, and mercury levels 1, 3
- Continue treatment until complete remission of proteinuria is achieved and mercury levels normalize 1, 2
- Follow up for at least 6-12 months after discontinuation of the fairness cream to ensure complete resolution 1, 2
Treatment Duration and Expected Outcomes
- Most patients show improvement within 6-9 months after discontinuing the mercury-containing cream and receiving appropriate treatment 1, 2
- Complete remission is typically achieved when both the nephrotic syndrome resolves and mercury levels normalize 1, 3
Special Considerations
- For patients with steroid-dependent or frequently relapsing nephrotic syndrome, consider steroid-sparing agents such as mycophenolate mofetil, rituximab, or cyclophosphamide 4, 8
- In cases of acute kidney injury, provide appropriate renal replacement therapy while continuing immunosuppressive treatment 4
- Consider genetic testing in steroid-resistant cases to rule out genetic causes of nephrotic syndrome 4