Kuno T, Hitomi T, Zaitu M, Sato T, Yoshida N, Miyazaki S
Department of Pediatrics, Saga Medical School, Nabeshima, Japan.
Acta Paediatr Jpn. 1998 Feb;40(1):85-7. doi: 10.1111/j.1442-200x.1998.tb01410.x.
A 12-year-old girl with severely decompensated abdominal Wilson disease was treated with abdominal dialysis in order to accelerate the excretion of chelated copper. Dialysate without human serum albumin or D-penicillamine was used and was able to accelerate the excretion of chelated copper, with an increment of 5.5-19.7% compared with urinary excretion only.
一名患有严重失代偿性腹型威尔逊病的12岁女孩接受了腹腔透析治疗,以加速螯合铜的排泄。使用了不含人血清白蛋白或D-青霉胺的透析液,其能够加速螯合铜的排泄,与仅通过尿液排泄相比,增加了5.5%-19.7%。