Al-Hawas F, Abdalla A H, Al-Sulaiman M H, Mousa D H, Owda A K, Al-Khader A A
Department of Nephrology, Riyadh Armed Forces Hospital, Saudi Arabia.
Am J Kidney Dis. 1997 Apr;29(4):631-2. doi: 10.1016/s0272-6386(97)90350-4.
We report a 38-year-old man who developed systemic lupus erythematosus (SLE) 14 years after commencing regular hemodialysis. When he was initially diagnosed as having end-stage renal disease (ESRD) secondary to chronic glomerulonephritis, he did not have any clinical or serological criteria to suspect SLE. He did not receive, at any stage, any of the drugs known to cause SLE. He showed remarkable improvement after treatment with steroids and cyclophosphamide.
我们报告一例38岁男性，在开始定期血液透析14年后发生系统性红斑狼疮（SLE）。当他最初被诊断为继发于慢性肾小球肾炎的终末期肾病（ESRD）时，他没有任何临床或血清学标准来怀疑SLE。在任何阶段，他都未使用过已知可引起SLE的药物。经类固醇和环磷酰胺治疗后，他病情显著改善。
