Table 1.
Classification of membranoproliferative glomerulonephritis
Membranoproliferative glomerulonephritis | Associated with systemic and infectious disorders |
---|---|
Idiopathic | |
Type I | |
Type II (dense deposit disease) | |
Type III | |
Secondary | |
Infectious diseases | Viral: Hepatitis B and C, human immunodeficiency virus |
Bacterial: shunt nephritis, visceral abscesses, infective endocarditis | |
Protozoal: quartan malaria, schistosomiasis, leprosy | |
Other: mycoplasma, mycobacteria | |
Systemic immune complex diseases | Mixed cryoglobulinemia |
Systemic lupus erythematosus | |
Scleroderma | |
Sjögren’s syndrome | |
Hereditary deficiencies of complement components | |
Hypocomplementemic urticarial vasculitis | |
Neoplasms | Leukemias and lymphomas |
Carcinomas | |
Light-chain disease and plasma cell dyscrasias | |
Chronic liver disease | Chronic hepatitis |
Cirrhosis | |
Miscellaneous | Partial lipodystrophy |
α1-Antitrypsin deficiency | |
Cystic fibrosis | |
Drugs (e.g. heroin, α-interferon) | |
Sarcoidosis | |
Sickle cell disease | |
Hemolytic uremic syndrome | |
Transplant glomerulopathy |