| (I) Common |
|
| (1) Light-chain cast nephropathy (myeloma kidney) |
|
| (2) Immunoglobulin-related amyloidosis (AL, AHL, and AH) |
|
| (3) Monoclonal immunoglobulin deposition disease (LCDD, LHCDD, and HCDD) |
|
| (4) Acute tubular necrosis |
|
| (A) Drugs (nonsteroidal anti-inflammatory drugs and bisphosphonates) |
|
| (B) Intravascular iodinated contrast |
|
| (5) Type I and type II cryoglobulinemic glomerulonephritis |
|
| (II) Uncommon |
|
| (1) Light chain proximal tubulopathy (with or without Fanconi syndrome) |
|
| (2) Crystal-storing histiocytosis |
|
| (3) Nonamyloid monoclonal fibrillary glomerulonephritis |
|
| (4) Immunotactoid glomerulonephritis/glomerulonephritis with organized microtubular monoclonal immunoglobulin deposits (GOMMID) |
|
| (5) C3 glomerulonephritis associated with monoclonal gammopathy |
|
| (6) Proliferative glomerulonephritis with monoclonal Ig deposits |
|
| (7) Hyperviscosity syndrome |
|
| (A) Waldenström's macroglobulinemia |
|
| (B) IgM, IgA, and rarely IgG myeloma |
|
| (8) Plasma cell infiltration |
|
| (9) Pyelonephritis |
|
| (10) Uric acid nephropathy |
|
