The gap between the number of kidneys available for transplantation and the number of recipients awaiting a kidney is growing. Consequently there is increasing interest in the donation of marginal kidneys [1]. Kidneys have been successfully transplanted from donors with known polycystic kidney disease [2], diabetic glomerulosclerosis [3], and horseshoe kidneys [4]. The reuse of a transplanted kidney has also been described [5]. Resolution of glomerular disease has been reported after transplantation of organs with diabetic glomerulosclerosis [3] and mesangial IgA deposits [6]. The presence of nephrotic syndrome in the donor has been considered a contra‐indication to transplantation; even a recent study of transplantation of pairs of ‘extended criteria’ donor kidneys excluded potential donors with greater than 3 g/24 h proteinuria [7]. We have been able to identify only one previous report of transplantation of kidneys from donors with nephrotic syndrome, and involving successful transplantation of kidneys from a donor with minimal‐change nephropathy; proteinuria rapidly resolved following transplantation [8]. Primary focal segmental glomerulosclerosis (FSGS) is thought to be caused by a circulating factor [9] and would therefore be expected to resolve following transplantation. We report successful renal transplantation, with resolution of proteinuria, from a cadaveric donor with FSGS who had nephrotic syndrome for 38 years.
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Rea et al. (2001) studied this question.
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