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. 2021 May 24;8:687149. doi: 10.3389/fmed.2021.687149

Table 4.

Classification of pathological manifestations of MG patients who underwent kidney biopsy.

Malignant neoplasms related lesions (N = 16) n (%) MGRS-related lesions (N = 43) n (%) MG-unrelated lesions (N = 42) n (%)
Amyloid nephropathy 8 (50.0%) Amyloid nephropathy 26 (60.5%) MN 16 (38.1%)
Glomerular minor lesion 2 (12.5%) MPGN 4 (9.3%) Diabetic glomerulosclerosis 4 (9.5%)
FSGS 1 (6.3%) MN 2 (4.7%) IgA nephropathy 3 (7.1%)
EPGN 1 (6.3%) Mesangioproliferative GN 2 (4.7%) FSGS 3 (7.1%)
MPGN 1 (6.3%) Mesangial nodular sclerosing glomerulopathy 2 (4.7%) MPGN 3 (7.1%)
LCDD 1 (6.3%) Subacute tubulointerstitial nephritis 2 (4.7%) Glomerular minor lesion 3 (7.1%)
HCDD 1 (6.3%) C3 GN 1 (2.3%) Proliferative-sclerosing GN 3 (7.1%)
TMA 1 (6.3%) EPGN 1 (2.3%) Subacute tubulointerstitial nephritis 2 (4.8%)
LCDD 1 (2.3%) Hypertensive renal disease 1 (2.4%)
TMA 1 (2.3%) LN 1 (2.4%)
Proliferative-sclerosing GN 1 (2.3%) EPGN 1 (2.4%)
Mesangioproliferative GN 1 (2.4%)
Hepatitis B virus-associated nephritis 1 (2.4%)

FSGS, focal segmental glomurular sclerosis; MN, membranous nephropathy; TMA, thrombotic microangiopathy; MPGN, membranoproliferative glomerulonephritis; LCDD, light chain deposition disease; HCDD, heavy chain deposition disease; EPGN, endocapillary proliferative glomerulonephritis; LN, lupus nephritis.