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Successful management of recurrent focal segmental glomerulosclerosis.
Kienzl-Wagner, Katrin; Rosales, Alejandra; Scheidl, Stefan; Giner, Thomas; Bösmüller, Claudia; Rudnicki, Michael; Oberhuber, Rupert; Margreiter, Christian; Soleiman, Afschin; Öfner, Dietmar; Waldegger, Siegfried; Schneeberger, Stefan.
Afiliação
  • Kienzl-Wagner K; Department of Visceral, Transplant and Thoracic Surgery, Medical University of Innsbruck, Innsbruck, Austria.
  • Rosales A; Department of Pediatrics, Medical University of Innsbruck, Innsbruck, Austria.
  • Scheidl S; Department of Visceral, Transplant and Thoracic Surgery, Medical University of Innsbruck, Innsbruck, Austria.
  • Giner T; Department of Pediatrics, Medical University of Innsbruck, Innsbruck, Austria.
  • Bösmüller C; Department of Visceral, Transplant and Thoracic Surgery, Medical University of Innsbruck, Innsbruck, Austria.
  • Rudnicki M; Department of Internal Medicine, Medical University of Innsbruck, Innsbruck, Austria.
  • Oberhuber R; Department of Visceral, Transplant and Thoracic Surgery, Medical University of Innsbruck, Innsbruck, Austria.
  • Margreiter C; Department of Visceral, Transplant and Thoracic Surgery, Medical University of Innsbruck, Innsbruck, Austria.
  • Soleiman A; Department of Pathology, Innsbruck State Hospital, Innsbruck, Austria.
  • Öfner D; Department of Visceral, Transplant and Thoracic Surgery, Medical University of Innsbruck, Innsbruck, Austria.
  • Waldegger S; Department of Pediatrics, Medical University of Innsbruck, Innsbruck, Austria.
  • Schneeberger S; Department of Visceral, Transplant and Thoracic Surgery, Medical University of Innsbruck, Innsbruck, Austria.
Am J Transplant ; 18(11): 2818-2822, 2018 11.
Article em En | MEDLINE | ID: mdl-29962080
ABSTRACT
Primary focal segmental glomerulosclerosis (FSGS) recurs in up to 55% of patients after kidney transplantation. Herein we report the successful management of recurrent FSGS. A 5-year-old boy with primary FSGS received a deceased donor renal transplant. Immediate and fulminant recurrence of FSGS caused anuric graft failure that was resistant to plasmapheresis and rituximab. After exclusion of structural or immunologic damage to the kidney by repeated biopsies, the allograft was retrieved from the first recipient on day 27 and transplanted into a 52-year-old second recipient who had vascular nephropathy. Immediately after retransplantation, the allograft regained function with excellent graft function persistent now at 3 years after transplant. After 2 years on hemodialysis, the boy was listed for kidney retransplantation. To prevent FSGS recurrence, pretreatment with ofatumumab was performed. Nephrotic range proteinuria still occurred after the second transplantation, which responded, however, to daily plasma exchange in combination with ofatumumab. At 8 months after kidney retransplantation graft function is good. The clinical course supports the hypothesis of a circulating permeability factor in the pathogenesis of FSGS. Successful ofatumumab pretreatment implicates a key role of B cells. Herein we provide a description of successful management of kidney failure by FSGS, carefully avoiding waste of organs.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glomerulosclerose Segmentar e Focal / Transplante de Rim / Anticorpos Monoclonais Humanizados / Rejeição de Enxerto / Antineoplásicos Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Child, preschool / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glomerulosclerose Segmentar e Focal / Transplante de Rim / Anticorpos Monoclonais Humanizados / Rejeição de Enxerto / Antineoplásicos Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Child, preschool / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article