Skip to main content
. 2020 Sep 3;11:2035. doi: 10.3389/fimmu.2020.02035

Table 2.

Pathological characteristics of patients with atypical anti-GBM disease.

Characteristic Total patients (N = 60)
Immunofluorescence
IgG linear deposition, n (%) 60 (100.0)
Intensity (scale 0~4+) 1.0 (1.0, 1.5)
Location (GBM/aTBM/Bowman's capsules), n (%) 60/37/5 (100.0/61.7/8.3)
IgG subclass (n = 59)
IgG1/IgG2/IgG3/IgG4, n (%) 27/21/7/11 (45.8/35.6/11.9/18.6)
IgA deposit, n (%) 27 (45.0)
IgM deposit, n (%) 33 (55.0)
C3 deposit, n (%) 39 (65.0)
C1q deposit, n (%) 10 (16.7)
bFRA deposit, n (%) 20 (33.3)
Albumin deposit, n (%) 38 (63.3)
Light microscopy
Number of glomeruli 25.0 (19.3, 36.0)
Crescent formation, n (%) 25 (41.7)
Percentage of crescents, % 27.3 (0.0, 49.7)
cTA/IF, n (%) 58 (96.7)
Electron microscopy
Electric dense deposit, n (%) 33 (55.9) (n = 59)
Combined dGN, n (%) 35 (58.3)
eIgAN (including fHSP-GN), n (%) 12 (20.0)
gMN, n (%) 8 (13.3)
hMPGN, n (%) 6 (10.0)
iAAV, n (%) 4 (6.7)
jFSGS, n (%) 3 (5.0)
kTBMN n (%) 1 (1.7)
lTMA, n (%) 1 (1.7)
a

TBM, tubular basement membrane;

b

FRA, fibrinogen-fibrin related antigens;

c

TA/IF, tubular atrophy and interstitial fibrosis;

d

GN, glomerulonephritis;

e

IgAN, IgA nephropathy;

f

HSP-GN, Henoch–Schönlein purpura glomerulonephritis;

g

MN, membranous nephropathy;

h

MPGN, membranoproliferative glomerulonephritis;

i

AAV, ANCA-associated vasculitis;

j

FSGS, focal segmental glomerulosclerosis;

k

TBMN, thin basement membrane nephropathy;

l

TMA, thrombotic microangiopathy.