| Literature DB >> 24842823 |
Yasuhiro Otsuka1, Asami Takeda, Keiji Horike, Daijyo Inaguma, Norihiko Goto, Yoshihiko Watarai, Kunio Morozumi.
Abstract
IgA nephropathy (IgAN) is recurrent after transplantation; however, its time of recurrence is unpredictable. To date, factors influencing IgAN recurrence have not been elucidated. We present a case of a 23-year-old man with end-stage renal disease (ESRD) who underwent living-related ABO-identical pre-emptive kidney transplantation (PEKT) using his 57-year-old mother as a donor. IgAN started when the patient was 19 years old, and renal biopsy revealed the usual pathological findings of IgAN. In spite of steroid therapy including steroid pulse and tonsillectomy, the patient developed nephrotic syndrome and progressed to ESRD in 4 years. Protocol biopsy on day 19 following PEKT revealed active recurrent IgAN. Nephrotic-range proteinuria and mild deterioration of kidney function developed regardless of strong immunosuppressive therapy such as steroid pulse, double filtration plasmapheresis and rituximab. We report a case of refractory IgAN that recurred 19 days after transplantation. This case is considered of value to elucidate factors leading to active IgAN recurrence.Entities:
Keywords: IgA nephropathy; early recurrence; recurrent IgA nephropathy; recurrent glomerulonephritis; renal transplantation
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Year: 2014 PMID: 24842823 DOI: 10.1111/nep.12252
Source DB: PubMed Journal: Nephrology (Carlton) ISSN: 1320-5358 Impact factor: 2.506