|
| (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 | |
|
