hrvatski

Membranoproliferativni glomerulonefritis u bolesnika sa sindromom sicca

Clinically significant renal disease is rare in sicca syndrome. The most well recognized renal histopa&not ; tologic lesion is an interstitial lymphocytic infiltrate with tubular atrophy and fibrosis which presents in tubular dysfunction. Glomerulonephritis is very rare in patients with sicca syndrome and only sporadic cases have been reported. The patient with sicca syndrome and membra&not ; noproliferative glomerulonephritis is presented.

Glomerulonefritis; membranoproliferativni; Sjogrenov sindrom

nije evidentirano

engleski

Membranoproliferative glomerulonephritis ina patients with sicca syndrome

Clinically significant renal disease is rare in sicca syndrome. The most well recognized renal histopa&not ; tologic lesion is an interstitial lymphocytic infiltrate with tubular atrophy and fibrosis which presents in tubular dysfunction. Glomerulonephritis is very rare in patients with sicca syndrome and only sporadic cases have been reported. The patient with sicca syndrome and membra&not ; noproliferative glomerulonephritis is presented.

Glomerulonephritis; membranoproliferative; Sjogren's syndrome

nije evidentirano