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Successful renal transplantation in Muckle–Wells syndrome treated with anti-IL-1β-monoclonal antibody
We report the first case of a 32-year-old woman with Muckle–Wells syndrome and biopsy-proven systemic AA amyloidosis and end-stage renal disease. She was treated with canakinumab 150 mg subcutaneously every 8 weeks and underwent renal transplantation. Fourteen months after renal transplanation, the...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421672/ https://www.ncbi.nlm.nih.gov/pubmed/25984207 http://dx.doi.org/10.1093/ndtplus/sfr118 |