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Repeated administrations of rituximab along with steroids and immunosuppressive agents in refractory steroid-resistant nephrotic syndrome

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Abstract

Background

A recent randomized control trial in children with steroid-resistant nephrotic syndrome revealed that two doses of rituximab did not reduce proteinuria.

Case characteristics

A 14-month-old boy developed refractory steroid-resistant nephrotic syndrome due to focal segmental glomerulosclerosis.

Observation

The patient achieved complete remission 11 months after disease onset following eight doses of rituximab combined with steroids and cyclosporine.

Message

Long-lasting B cell depletion with repeated rituximab administrations may be required to achieve complete remission in patients with steroid-resistant nephrotic syndrome and massive proteinuria.

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Correspondence to Shuichiro Fujinaga.

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Fujinaga, S., Sakuraya, K. Repeated administrations of rituximab along with steroids and immunosuppressive agents in refractory steroid-resistant nephrotic syndrome. Indian Pediatr 54, 49–50 (2017). https://doi.org/10.1007/s13312-017-0996-3

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  • DOI: https://doi.org/10.1007/s13312-017-0996-3

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