Khan M A, Akhtar M, Taher S M
King Faisal Specialist Hospital, Riyadh, Saudi Arabia.
Am J Nephrol. 1988;8(3):235-9. doi: 10.1159/000167589.
Glomerulonephritis complicating primary Sjögren's syndrome is extremely rare, with only 3 cases of membranoproliferative glomerulonephritis reported in the literature. We report on a 55-year-old woman with a long-standing history of dryness of the mouth and eyes who was found to have nephrotic syndrome. Extensive investigations indicated primary Sjögren's syndrome. Kidney biopsy revealed a membranoproliferative glomerulonephritis. Treatment with prednisone and cyclophosphamide resulted in complete remission of nephrotic syndrome. The pathogenesis of glomerulonephritis appears to be due to deposition of circulating immune complexes.
肾小球肾炎并发原发性干燥综合征极为罕见,文献中仅报道过3例膜增生性肾小球肾炎。我们报告一例55岁女性,有长期口眼干燥病史,被发现患有肾病综合征。广泛检查提示原发性干燥综合征。肾活检显示为膜增生性肾小球肾炎。泼尼松和环磷酰胺治疗使肾病综合征完全缓解。肾小球肾炎的发病机制似乎是由于循环免疫复合物的沉积。