Dyck R F, Katz A, Gordon D A, Johnson M, Shainhouse Z, Cardella C J, Bear R A
J Rheumatol. 1979 May-Jun;6(3):336-44.
Five patients with primary idiopathic polymyositis developed proteinuria associated with urine sediment abnormalities. Renal biopsies disclosed a focal mesangial proliferative glomerulonephritis with deposits of immunoglobulin and complement. After treatment of the polymyositis with corticosteroids, proteinuria and urine sediment changes disappeared within 4 to 8 wk along with an improvement in the muscle disease. Although the pathogenesis remains to be determined, immune complexes may be implicated in the etiology of this renal lesion.
5例原发性特发性多发性肌炎患者出现蛋白尿并伴有尿沉渣异常。肾活检显示局灶性系膜增生性肾小球肾炎,伴有免疫球蛋白和补体沉积。用皮质类固醇治疗多发性肌炎后,蛋白尿和尿沉渣改变在4至8周内消失,同时肌肉疾病有所改善。虽然发病机制尚待确定,但免疫复合物可能与这种肾脏病变的病因有关。