Stefanov G, Beleva B, Doĭchinov D, Minkov N
Vutr Boles. 1988;27(2):130-3.
A case is presented of a 19-year-old man suffering from focal-segmental glomerulosclerosis with terminal chronic renal failure to whom a kidney taken from his mother was transplanted. There was high blood-group and tissue compatibility between mother and son. The initial result was good, the transplanted kidney functioned well-diuresis of 3300 ml with high proteinuria. Gradually the diuresis fell to 100-200 ml. From the 29th day following the transplantation pulse urbason therapy was applied for 3 days but without effect. This led to the resumption of hemodialysis and removal of the transplanted kidney. The microscopic examination of the kidney revealed massive focal-segmental glomerulosclerosis which had led to terminal chronic renal failure. The rapid severe relapse of the disease in the transplanted kidney is explained with the malignancy of the disease and the very high compatibility between donor and recipient. It is recommended that renal transplantation in patients with focal-segmental glomerulosclerosis should not be performed with a kidney taken from a parent.
本文报告一例19岁患有局灶节段性肾小球硬化症并发展至终末期慢性肾衰竭的男性患者,接受了来自其母亲的肾脏移植。母子之间血型和组织相容性良好。初期结果良好,移植肾功能正常,尿量达3300毫升,但蛋白尿较高。随后尿量逐渐降至100 - 200毫升。移植后第29天开始应用脉冲式强的松龙治疗3天,但无效。这导致恢复血液透析并摘除移植肾。对摘除的肾脏进行显微镜检查发现大量局灶节段性肾小球硬化,这是导致终末期慢性肾衰竭的原因。移植肾中疾病迅速严重复发的原因是该疾病的恶性程度以及供体和受体之间非常高的相容性。建议患有局灶节段性肾小球硬化症的患者不应接受来自父母的肾脏进行肾移植。