Renal Pathology

Collagenofibrotic Glomerulopathy

J. Charles Jennette
University of North Carolina
Chapel Hill NC


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Clinical History
The patient was a 19 year-old Caucasian female with nephrotic range proteinuria. Laboratory data included blood pressure 110/80 mmHg, trace peripheral edema, no skin lesions, no hematuria, 4 to 5 grams of proteinuria per 24-hours, serum creatinine 0.6 mg/dl, creatinine clearance 90-110 ml/min, normal serum C3 and C4, negative ANA, and negative HBV serology.

Light microscopy and electron microscopy images are available to evaluate. Immunofluorescence microscopy demonstrated slight granular mesangial and capillary wall staining for C3 but no staining for IgG, IgA, IgM, kappa light chains, lambda light chains, C1q or fibrin.


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Figure 1
Low power view of cortex, H&E stain

Figure 2
Representative glomerulus, high power, with H&E stain

Figure 3
Representative glomerulus, high power, with PAS stain

Figure 4
Representative glomerulus, high power, with trichrome stain

Figure 5
Glomerulus stained with antibody to C3 (B&W)

Figure 6
Electron micrograph of representative glomerulus

Figure 7
Electron micrograph of representative glomerulus