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. 2021 Aug 3;100(6):1303–1315. doi: 10.1016/j.kint.2021.07.015

Table 5.

Diagnoses reported within the literature of COVID-19 kidney biopsies (n = 158 native and 7 allograft biopsies)

Diagnosis Number of cases Frequency of cases in literature, % Published references
Native kidney biopsies (n = 159)
Collapsing glomerulopathy 58 36.7 7, 8, 9,15,20,21,28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42
Acute tubular injury 46 29.1 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 7, 8, 9
FSGS, noncollapsing 8 5.1 9,19,20,28
Thrombotic microangiopathy 7 4.4 7,9,16,20,25,26
Crescentic GN, pauci-immune 7 4.4 20,50,51
IgA nephropathy 6 3.8 20,41,47, 48, 49
Minimal change disease 5 3.2 8,9,21
Membranous glomerulopathy 5 3.2 8,20,41
Diabetic glomerulopathy 4 2.5 9,11,14,16,26,41
Oxalate nephropathy 2 1.3 14,43
Anti-GBM antibody disease 2 1.3 45,46
Granulomatous tubulointerstitial nephritis 1 0.6 27
Acute interstitial nephritis 1 0.6 14
Lupus nephritis 1 0.6 8
MPGN, immune complex type (COVIC) 1 0.6 44
Infection-associated glomerulonephritis 1 0.6 9
Cortical infarct 1 0.6 8
Arteritis 1 0.6 20
Amyloidosis 1 0.6 11,20
Light chain cast nephropathy 1 0.6 20
Transplant kidney biopsies (n = 7)
Antibody-mediated rejection 2 28.6 9
T cell–mediated rejection 1 14.3 8
Acute tubular injury 1 14.3 22
Calcineurin inhibitor nephrotoxicity 1 14.3 20
Collapsing glomerulopathy 1 14.3 42
Severe IF/TA 1 14.3 20

COVIC, COVID-19–associated immune complex disease; COVID-19, coronavirus disease 2019; FSGS, focal segmental glomerulosclerosis; GBM, glomerular basement membrane; GN, glomerulonephritis; IF, interstitial fibrosis; MPGN, membranoproliferative glomerulonephritis; TA, tubular atrophy.