Plasmapheresis-induced remission in otherwise therapy-resistant FSGS

We report an 8-year-old Caucasian boy who presented with steroid-resistant nephrotic syndrome. Renal biopsy showed the cellular variant of focal segmental glomerulosclerosis (FSGS). Within 1 year he received a series of therapies that have induced remission in other patients with this disease, all t...

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Published in:Pediatric nephrology (Berlin, West) Vol. 16; no. 11; pp. 898 - 900
Main Authors: VECSEI, Andreas K. W, MÜLLER, Thomas, SCHRATZBERGER, Edith C, KIRCHER, Karl, REGELE, Heinz, ARBEITER, Klaus, SCHROTH, Brigitte, AUFRICHT, Christoph
Format: Conference Proceeding Journal Article
Language:English
Published: Heidelberg Springer 01-11-2001
Springer Nature B.V
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Summary:We report an 8-year-old Caucasian boy who presented with steroid-resistant nephrotic syndrome. Renal biopsy showed the cellular variant of focal segmental glomerulosclerosis (FSGS). Within 1 year he received a series of therapies that have induced remission in other patients with this disease, all to no avail (conventional-dose cyclosporin A, methylprednisolone pulse therapy, high-dose cyclosporin A, and therapy with mycophenolate mofetil). He achieved remission after five sessions of plasma exchange. This case argues for aggressive therapy of resistant nephrotic syndrome in the native kidney. Plasma exchange should be considered as a possible rescue therapy arm in future study protocols.
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ISSN:0931-041X
1432-198X
DOI:10.1007/s004670100682