Partial Fanconi syndrome induced by imatinib therapy: A novel cause of urinary phosphate loss

被引:48
作者
Francois, Helene [1 ,2 ]
Coppo, Paul [3 ]
Hayman, Jean-Philippe [1 ,2 ]
Fouqueray, Bruno [1 ,2 ]
Mougenot, Beatrice [4 ]
Ronco, Pierre [1 ,2 ]
机构
[1] Tenon Hosp, Dept Nephrol & Dialysis, AP HP, F-75020 Paris, France
[2] Univ Paris 06, Paris, France
[3] Hop St Antoine, AP H, Dept Haematol, F-75571 Paris, France
[4] Tenon Hosp, Dept Pathol, AP HP, F-75020 Paris, France
关键词
fanconi syndrome; imatinib; hypophosphaternia; hypouricemia; renal failure;
D O I
10.1053/j.ajkd.2007.10.039
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Imatinib mesylate (Gleevec, Glivec; Novartis, Basel, Switzerland) is a specific tyrosine kinase inhibitor that has become the gold-standard treatment for patients with chronic myeloid leukemia. Several tyrosine kinases inhibited by imatinib are expressed in the kidney, and although the drug is usually well tolerated, several cases of acute renal failure were reported. We describe for the first time a case of a patient treated by imatinib for chronic myeloid leukemia who developed partial Fanconi syndrome with mild renal failure, which leads to a discussion of the pathophysiological characteristics of imatinibinduced renal toxicity. Patients on long-term imatinib treatment should be monitored for renal failure, as well as proximal tubule dysfunction, including hypophosphatemia. Am J Kidney Dis 51:298-301. (c) 2008 by the National Kidney Foundation, Inc.
引用
收藏
页码:298 / 301
页数:4
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