F. Yoshida et al., NEPHROTIC SYNDROME WITH MASSIVE ACCUMULATION OF TYPE-I AND TYPE-III COLLAGEN IN THE GLOMERULI, Internal medicine, 32(2), 1993, pp. 171-176
A 54-year-old woman with nephrotic syndrome underwent renal biopsy. By
light microscopy, the glomerular capillary lumen was remarkably narro
wed because of diffuse accumulation of Periodic acid Shiff (PAS) posit
ive material along the glomerular capillary wall. By electron microsco
py, collagenous fibers were observed in the mesangium and subendotheli
al area. The fibrous material reacted with antibodies against type I a
nd III collagen but not with those against laminin or type IV collagen
by an indirect immunofluorescence technique. This case seemed to be a
case of collagenofibrotic glomerulonephropathy.