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Recurrence of focal segmental glomerulosclerosis in renal allograft: An in-depth review
被引:95
|作者:
Vinai, Modini
[1
,2
]
Waber, Pamela
[1
]
Seikaly, Mouin G.
[1
,2
]
机构:
[1] Univ Texas Dallas, SW Med Ctr, Dept Pediat, Dallas, TX 75235 USA
[2] Childrens Med Ctr, Dept Pediat, Dallas, TX 75235 USA
关键词:
FSGS;
transplant;
kidney;
recurrence;
children;
IDIOPATHIC NEPHROTIC SYNDROME;
GLOMERULAR ALBUMIN PERMEABILITY;
KIDNEY-TRANSPLANT RECIPIENTS;
POSTTRANSPLANTATION RECURRENCE;
PATHOLOGICAL CLASSIFICATION;
PLASMAPHERESIS TREATMENT;
CYCLOSPORINE THERAPY;
RITUXIMAB TREATMENT;
CIRCULATING FACTOR;
NPHS2;
MUTATION;
D O I:
10.1111/j.1399-3046.2009.01261.x
中图分类号:
R72 [儿科学];
学科分类号:
100202 ;
摘要:
Focal segmental glomerulosclerosis is a major cause of chronic kidney disease requiring transplantation in children. Recurrence rate in the renal allograft transplantation is as high as 50%. Recurrence of FSGS is associated with renal dysfunction and early graft loss. To date, there is no established therapy for recurrent FSGS after renal transplant. We have reviewed the current English literature in order to summarize current practices with emphasis on graft outcome. We conclude that despite multiple approaches to the post transplant management of recurrent FSGS, none have been shown to be consistently beneficial. Currently, pheresis combined with high dose anti-calcineurin with or without rituximab seems to be the most promising. Further controlled studies are needed to define the optimal therapeutic regimens to treat recurrent of FSGS.
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页码:314 / 325
页数:12
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