Drachman R, Dollberg L, Drukker A
Division of Pediatric Nephrology, Shaare Zedek Medical Center, Jerusalem, Israel.
Child Nephrol Urol. 1988;9(1-2):90-2.
A 14.5-year-old boy with end-stage renal failure due to familial primary hyperoxaluria underwent cadaver donor renal transplantation. The graft function was stable for a period of 22 months, while he was on conventional immunosuppressive therapy (prednisolone and azathioprine) and additional oral pyridoxine, phosphorus, and magnesium supplementation. When ciclosporin A was introduced instead of azathioprine, the blood levels of oxalate rose, and oxalate deposition in the renal tubuli became evident. These observations suggest that ciclosporin A interferes with oxalate metabolism and, therefore, should be given with utmost caution in patients with primary hyperoxaluria.
一名14.5岁因家族性原发性高草酸尿症导致终末期肾衰竭的男孩接受了尸体供肾肾移植。在他接受传统免疫抑制治疗(泼尼松龙和硫唑嘌呤)并额外口服补充吡哆醇、磷和镁的期间,移植肾的功能稳定了22个月。当用环孢素A替代硫唑嘌呤时,血草酸水平升高,肾小管中的草酸盐沉积变得明显。这些观察结果表明,环孢素A会干扰草酸代谢,因此,对于原发性高草酸尿症患者,使用时应极其谨慎。