Benabdallah Leila, Rerolle Jean-Philippe, Peraldi Marie-Noelle, Noël Laure-Hèléne, Bruneel Marie-France Mamzer, Carron Pierre-Louis, Morelon Emmanuel, Kreis Henri
Department of Renal Transplantation, Necker Hospital, Paris, France.
Am J Kidney Dis. 2002 Dec;40(6):E20. doi: 10.1053/ajkd.2002.36931.
The recurrence of immunoglobulin A nephropathy (IgAN) after renal transplantation has been described in 40% to 50% of cases. For a long time, this type of recurrence was considered as a benign condition. However, recent data have shown that recurrent IgAN has become a significant cause of long-term allograft loss. The authors present here the case of a 47-year-old man with IgAN, which led to end-stage renal failure in 1999. In November 2000, he received a cadaveric renal allograft. Ten months later, acute nephritic syndrome and rapidly progressive renal failure developed. Renal biopsy showed extracapillary glomerulonephritis with crescent formation in one third of the glomeruli associated with necrosis. Steroid treatment was unsuccessful, and renal function progressively deteriorated with a creatinine level at 3.7 mg/dL 6 months after diagnosis of recurrence. This patient's graft probably will be lost in a few months.
肾移植后免疫球蛋白A肾病(IgAN)的复发率在40%至50%的病例中已有报道。长期以来,这种类型的复发被认为是一种良性情况。然而,最近的数据表明,复发性IgAN已成为长期移植肾丢失的一个重要原因。作者在此介绍了一名47岁IgAN男性患者的病例,该患者于1999年发展为终末期肾衰竭。2000年11月,他接受了尸体肾移植。十个月后,出现急性肾炎综合征和快速进行性肾衰竭。肾活检显示为毛细血管外肾小球肾炎,三分之一的肾小球有新月体形成并伴有坏死。类固醇治疗无效,复发诊断6个月后,肾功能逐渐恶化,肌酐水平达到3.7mg/dL。该患者的移植肾可能在几个月内丧失。