Chen Y C, Yeh J C, Chen H S, Hsu H C
Department of Internal Medicine, Mackay Memorial Hospital, Taipei, Taiwan, Republic of China.
Clin Nephrol. 1990 Mar;33(3):148-51.
A 61-year-old male patient had secondary polycythemia associated with idiopathic nephrotic syndrome. Renal biopsy revealed membranous nephropathy. Polycythemia did not change in spite of partial remission of proteinuria. Serum erythropoietin determined by an enzyme-linked immunosorbent assay was 7.2 mU/ml. His serum erythropoietin maintained at a constant level during polycythemia was higher than it was before the appearance of renal ischemia, so he was kept in a polycythemic state. Whether decreasing proteinuria can improve renal ischemia requires future study. We must observe the patient for the occurrence of thromboembolism. Renal ischemia possibly induced by nephrotic syndrome is likely to cause secondary polycythemia.
一名61岁男性患者患有与特发性肾病综合征相关的继发性红细胞增多症。肾活检显示为膜性肾病。尽管蛋白尿部分缓解,但红细胞增多症并未改变。通过酶联免疫吸附测定法测定的血清促红细胞生成素为7.2 mU/ml。在红细胞增多症期间,他的血清促红细胞生成素维持在恒定水平,高于肾缺血出现之前,因此他一直处于红细胞增多状态。降低蛋白尿是否能改善肾缺血需要未来进一步研究。我们必须观察患者是否发生血栓栓塞。肾病综合征可能诱发的肾缺血很可能导致继发性红细胞增多症。