McLeish K R, Gohara A F, Shapiro R S
Transplantation. 1980 May;29(5):392-6. doi: 10.1097/00007890-198005000-00009.
Three patients developed massive proteinuria, hypoalbuminemia, and edema after transplantation. These findings occurred in the immediate post-transplant period in two patients, and renal failure developed. The third patient developed proteinuria 4 months post-transplantation. There was complete remission of proteinuria in two patients and recovery of renal function in one. Renal histology was similar in all. Light microscopy demonstrated that the glomeruli contained a mild increase in mesangial matrix, but were otherwise normal. No significant interstitial cellular infiltration or fibrosis was present. Immunofluorescence microscopy revealed no staining for immunoglobulins or complement. Electron microscopy demonstrated fusion of foot processes, but the glomerular basement membrane was normal. No electron-dense deposits were found. The usual causes of post-transplant nephrotic syndrome were ruled out. We believe these three patients represent a unique disorder of the transplanted kidney.
三名患者在移植后出现大量蛋白尿、低白蛋白血症和水肿。其中两名患者在移植后即刻出现这些表现,并发展为肾衰竭。第三名患者在移植后4个月出现蛋白尿。两名患者的蛋白尿完全缓解,一名患者肾功能恢复。所有患者的肾脏组织学表现相似。光镜检查显示肾小球系膜基质轻度增加,但其他方面正常。未发现明显的间质细胞浸润或纤维化。免疫荧光显微镜检查未发现免疫球蛋白或补体染色。电镜检查显示足突融合,但肾小球基底膜正常。未发现电子致密沉积物。排除了移植后肾病综合征的常见病因。我们认为这三名患者代表了一种移植肾的独特疾病。