Recurrent primary hyperoxaluria type 2 leads to early post-transplant renal function loss: A case report

نویسندگان

  • Si Liu
  • Baoshan Gao
  • Gang Wang
  • Weigang Wang
  • Xin Lian
  • Shan Wu
  • Jinyu Yu
  • Yaowen Fu
  • Honglan Zhou
چکیده

Primary hyperoxaluria type 2 is a rare autosomal recessive disorder caused by glyoxylate reductase/hydroxypyruvate reductase deficiency and characterized by recurrent episodes of nephrolithiasis and nephrocalcinosis. Herein, we describe a case of primary hyperoxaluria type 2 in a 33-year-old man who failed to respond to conventional therapies; thus renal transplantation was performed. This case demonstrated that, although primary hyperoxaluria type 2 is rare, hyperoxaluria should be suspected and blood oxalate and stone component be examined in patients with recurrent episodes of nephrolithiasis, particularly in those who are unresponsive to conventional therapies. Combined liver-kidney transplant may be required as kidney transplant alone is not likely to be successful.

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عنوان ژورنال:

دوره 15  شماره 

صفحات  -

تاریخ انتشار 2018