Table 3.
Differential diagnosis of immune-mediated glomerular lesions with fibrillar/microtubular substructure
| Special stains | Structure | Diameter, nm | Orientation | Most common glomerular distribution | Extraglomerular involvement | |
|---|---|---|---|---|---|---|
| Amyloid | Congo red, thioflavin T [42] | Fibril | 8–12 | Random, nonbranching | Mesangium, subendothelial, intramembranous, subepithelial | Yes |
|
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| FGN | DNAJB9 immunohistochemistry [6] | Fibril | 16–24 | Random, nonbranching | Mesangium, subendothelial, intramembranous, subepithelial | Rare |
|
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| ITG | Microtubule, hollow core | 30–50 | Elongated, often parallel arrays | Mesangium, subendothelial, intramembranous, subepithelial | Rare | |
|
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| Cryoglobulinic glomerulonephritis | Cylindrical/annular; hollow core | 30–35 | Short, randomly oriented | Subendothelial, capillary lumen, mesangium | Sometimes (vascular) | |
|
| ||||||
| Lupus nephritis | Fibrils/tubules | 10–100 [43] | Fingerprint- like | mesangial, subendothelial, and/or subepithelial | Yes | |
FGN, fibrillary glomerulonephritis; ITG, immunotactoid glomerulopathy.