Cortez M S, Sturgill B C, Bolton W K
Division of Nephrology, University of Virginia Health Sciences Center, Charlottesville, USA.
Am J Kidney Dis. 1995 Apr;25(4):632-6. doi: 10.1016/0272-6386(95)90136-1.
Glomerular involvement in primary Sjögren's syndrome is rare and only five cases of membranoproliferative glomerulonephritis have been reported. We present a case of a 31-year-old white woman with primary Sjögren's syndrome who developed nephrotic syndrome. Evaluation showed no evidence of an associated connective tissue disease. Kidney biopsy was consistent with type I membranoproliferative glomerulonephritis. The patient's nephrotic syndrome resolved spontaneously, a course that has not been reported previously in this setting.
原发性干燥综合征累及肾小球的情况罕见,仅有5例膜增生性肾小球肾炎的报道。我们报告一例31岁患原发性干燥综合征的白人女性,她出现了肾病综合征。评估显示没有相关结缔组织病的证据。肾活检符合I型膜增生性肾小球肾炎。患者的肾病综合征自发缓解,这种病程在此情况下此前未见报道。