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Definitions of glomerular lesions derived from the Oxford classification of IgA nephropathy and patterns of glomerulonephritis derived from the ISN/RPS lupus classification

Definitions of glomerular lesions derived from the Oxford classification of IgA nephropathy and patterns of glomerulonephritis derived from the ISN/RPS lupus classification
Glomerular lesions
Mesangial hypercellularity >3 mesangial cells per mesangial area
Cellular crescent Extracapillary cell proliferation of more than two cell layers with >50% of the lesion occupied by cells
Fibrocellular crescent An extracapillary lesion comprising cells and extracellular matrix, with <50% cells and <90% matrix
Fibrous crescent Extracapillary crescents with >90% matrix
Endocapillary hypercellularity Hypercellularity caused by an increased number of cells within glomerular capillary lumina, causing narrowing of the lumina
Fibrinoid necrosis Disruption of the GBM with fibrin exudation
Sclerosis Obliteration of the capillary lumen by increased extracellular matrix with or without hyalinosis or foam cells
Patterns of GN
Minimal mesangial GN* Normal glomeruli by LM but mesangial immune deposits by IF
Mesangial proliferative GN* Purely mesangial hypercellularity
Active (proliferative) GN* Any or all of the following glomerular lesions: endocapillary hypercellularity, karyorrhexis, fibrinoid necrosis, rupture of GBMs, cellular or fibrocellular crescents, subendothelial deposits identifiable by LM, and intraluminal immune aggregates
Necrotizing GN Segmental or global fibrinoid necrosis
Crescentic GN ≥50% glomeruli with cellular, fibrocellular, or fibrous crescents (with percentage of crescents always noted in the diagnostic line, even when <50%)
Membranoproliferative GN Mesangial and/or endocapillary hypercellularity and thickening of capillary walls caused by subendothelial Ig and/or complement factors
Exudative GN Neutrophils accounting for >50% of glomerular hypercellularity
Sclerosing GN* Any or all of the following glomerular lesions: glomerular sclerosis, fibrous adhesions, and fibrous crescents

ANCA: antineutrophil cytoplasmic autoantibody; C3GN: C3 glomerulonephritis; GBM: glomerular basement membrane; GN: glomerulonephritis; IF: immunofluorescence; Ig: immunoglobulin; IgA: immunoglobulin A; ISN/RPS: International Society of Nephrology/Renal Pathology Society; LM: light microscopy.

* Except for the first two patterns, multiple patterns can occur together in a single specimen (derived from the ISN/RPS lupus classification[1]).

¶ The term crescentic GN is used when crescents are present in at least 50% of glomeruli and applies to immune-complex C3GN glomerulopathy. This does not apply to ANCA GN and anti-GBM GN, where less than 50% of the glomeruli may be involved by crescents.
Reference:
  1. Falk RJ, Nachman PH, Hogan SL, Jennette JC. ANCA glomerulonephritis and vasculitis: A Chapel Hill perspective. Semin Nephrol 2000; 20:233.

Reproduced with permisison from: Sethi S, Haas M, Markowitz GS, et al. Mayo Clinic/Renal Pathology Society consensus report on pathologic classification, diagnosis, and reporting of GN. J Am Soc Nephrol 2016; 27(5):1278-1287. Copyright © 2016 American Society of Nephrology. https://journals.lww.com/jasn/pages/default.aspx.

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