Table 1 Renal histology in cases of nephrotic-range proteinuria in autosomal dominant polycystic kidney disease patients reported in the literature so far.
No. | First author [Ref. No.] Year | Renal histopathology |
|---|---|---|
1 | Kida [6] 1972 | Focal glomerulosclerosis and/or minimal change disease |
2 | Murphy [7] 1990 | Focal glomerulosclerosis |
3 | Montoyo [4] 1992 | Focal glomerulosclerosis |
4 | Dionisio [8] 1993 | Focal glomerulosclerosis |
5 | Contreas [3] 1995 | Focal glomerulosclerosis |
6 | Abe [9] 1985 | Membranous glomerulonephritis |
7 | Shikata [10] 1991 | Membranous glomerulonephritis |
8 | Saxena [11] 1993 | Membranous glomerulonephritis |
9 | Nakahama [12] 1991 | Minimal change disease |
10 | Kuroki [13] 1995 | Minimal change disease |
11 | Panisello [14] 1988 | Immunoglobulin A nephropathy |
12 | Hiura [15] 2006 | Immunoglobulin A nephropathy |
13 | Licina [16] 1981 | Crescentic glomerulonephritis |
14 | Hariharan [17] 1987 | Intercapillary diabetic glomerulosclerosis |
15 | Villar [18] 1992 | Type 1 membranoproliferative glomerulonephritis |
16 | Villar [18] 1992 | Mesangioproliferative glomerulonephritis |
17 | Seyrek [19] 1995 | Mesangioproliferative glomerulonephritis |
18 | Sar [20] 2007 | Amyloidosis |
19 | Index case | Diffuse proliferative glomerulonephritis |