Version May 2024
| Plasma cell disorders |
| Monoclonal gammopathy of undetermined significance (MGUS) |
| Biclonal gammopathy of undetermined significance |
| Idiopathic Bence Jones proteinuria |
| Monoclonal gammopathy of renal significance (MGRS) |
| POEMS syndrome, osteosclerotic myeloma |
| Castleman disease |
| AL (light chain) amyloidosis, light chain and heavy chain deposition diseases |
| Solitary plasmacytoma |
| Multiple myeloma, smoldering multiple myeloma |
| B cell lymphoproliferative disorders |
| Non-Hodgkin lymphoma |
| Chronic lymphocytic leukemia |
| Lymphoplasmacytic lymphoma (Waldenström macroglobulinemia) |
| Post-transplant monoclonal gammopathies |
| Heavy chain diseases |
| Connective tissue disorders* |
| Systemic lupus erythematosus |
| Rheumatoid arthritis |
| Sjögren syndrome |
| Scleroderma |
| Psoriatic arthritis |
| Polymyalgia rheumatic |
| Infections* |
| Hepatitis C virus infection |
| HIV/AIDS |
| Dermatologic disorders |
| Scleredema (scleromyxedema), lichen myxedematosus |
| Diffuse plane xanthomatosis |
| Urticaria and IgM (Schnitzler's syndrome) |
| Subcorneal pustular dermatosis |
| Necrobiotic xanthogranuloma |
| Pyoderma gangrenosum |
| Renal disorders |
| Antiglomerular basement membrane disease |
| C3 glomerulonephritis |
| Dense deposit disease |
| Fibrillary glomerulonephritis |
| Light chain proximal tubulopathy |
| Membranous nephropathy |
| Monoclonal immunoglobulin deposition disease |
| Proliferative glomerulonephritis with monoclonal immunoglobulin deposits |
| Neurologic disorders |
| CANOMAD (chronic ataxic neuropathy, ophthalmoplegia, IgM paraprotein, cold agglutinins, and disialosyl antibodies) |
| Sensorimotor neuropathy with MGUS |
| Sporadic late-onset nemaline myopathy |
| Corneal copper deposition |
| Crystalline keratopathy |
| Miscellaneous disorders* |
| Acquired von Willebrand disease |
| Acquired C1 esterase inhibitor deficiency (angioedema) |
| Cryoglobulinemia |
| Capillary leak syndrome |
| Cold agglutinin disease |
| Insulin autoimmune syndrome |
| TEMPI (telangiectasias, erythrocytosis with elevated erythropoietin, MGUS, perinephric fluid collections, and intrapulmonary shunting) |
| Crystal-storing histiocytosis |
| Gaucher disease |
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