Tejani A, Phadke K, Adamson O, Nicastri A, Chen C K, Sen D
Nephron. 1985;39(4):352-5. doi: 10.1159/000183404.
Sickle cell nephropathy characterized by proteinuria and predominantly glomerular lesions has not been studied as extensively as renal tubular alterations in sickle cell disease. We reviewed our experience with this entity over a 14-year period. Of 13 children with either proteinuria or the nephrotic syndrome, 8 showed focal and segmental glomerulosclerosis, and 5 had mesangial proliferation. Children with focal and segmental glomerulosclerosis were older at onset of nephropathy and presented with the nephrotic syndrome more frequently than those with mesangial proliferation (p less than 0.05). All patients with mesangial proliferation and half of the focal and segmental glomerulosclerosis patients had supranormal renal clearances at onset of nephropathy suggesting hyperfiltration. Hyperfiltration seen in animals with reduced renal mass, and in human diabetic nephropathy before reduction in nephron units leads to mesangial proliferation and sclerosis. Our study suggests that sickle cell disease produces similar lesions in patients with sickle cell nephropathy.
以蛋白尿和主要为肾小球病变为特征的镰状细胞肾病,其研究不如镰状细胞病中的肾小管改变那样广泛。我们回顾了14年间对这一病症的诊治经验。在13例患有蛋白尿或肾病综合征的儿童中,8例表现为局灶节段性肾小球硬化,5例有系膜增生。与系膜增生的患儿相比,局灶节段性肾小球硬化的患儿肾病起病时年龄更大,肾病综合征的发生率更高(P<0.05)。所有系膜增生的患者以及半数局灶节段性肾小球硬化的患者在肾病起病时肾清除率高于正常,提示存在超滤过。在肾单位减少的动物以及人类糖尿病肾病在肾单位减少之前所见到的超滤过会导致系膜增生和硬化。我们的研究提示,镰状细胞病在镰状细胞肾病患者中产生类似的病变。