Smeitink J, Verreussel M, Schröder C, Lippens R
Department of Paediatrics, University Hospital, Nijmegen, The Netherlands.
Eur J Pediatr. 1988 Nov;148(2):164-6. doi: 10.1007/BF00445929.
Three patients developed a Fanconi syndrome with impairment of glomerular function (endogenous creatinine clearance 30-60 ml/min per 1.73 m2) during and/or after treatment with ifosfamide according to the SIOP-MMT 84 protocol in which ifosfamide was given in a dose of 3000 mg/m2 every 4 weeks over a 10-month period. The need for early substitution therapy in patients with the Fanconi syndrome is stressed. The renal lesions in our patients were irreversible.
根据SIOP-MMT 84方案,3例患者在异环磷酰胺治疗期间和/或治疗后出现了范科尼综合征,伴有肾小球功能损害(内生肌酐清除率为每1.73平方米30 - 60毫升/分钟),该方案中异环磷酰胺的给药剂量为每4周3000毫克/平方米,持续10个月。强调了对范科尼综合征患者进行早期替代治疗的必要性。我们患者的肾脏病变是不可逆的。