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(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 | |
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