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| __NOTOC__
| | #Redirect[[Nephritic syndrome#Classification]] |
| {{Nephritic syndrome}}
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| {{CMG}}
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| ==Classification==
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| Acute nephritic syndrome may be differentiated according to the etiology of renal disease. Acute nephritis may be classified based on renal vs. non-renal etiology. Similarly, acute nephritis may be classified as idiopathic vs. secondary to other conditions. Finally, diseases may be classified according to the proliferative vs. non-proliferative changes seen on pathology.
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| The following tables shows the classification of acute glomerulonephritis:
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| {| border="1" style="border-collapse:collapse; text-align:left;" cellpadding="5" align="center"
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| |+ '''''Classification of Glomerular Diseases'''''
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| | bgcolor="#d9ff54"|'''Type of Disorder''' || bgcolor="#d9ff54"|'''Proliferative Changes'''|| bgcolor="#d9ff54"|'''No Proliferative Changes'''
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| |-
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| | bgcolor="#ececec"|'''Primary Renal Disorder ''' ||
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| *IgA nephropathy
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| *IgM nephropathy
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| *Other mesangioproliferative glomerulonephritides
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| *Crescentic glomerulonephritis
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| **With immune deposits
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| **Pauci-immune
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| *Membranoproliferative glomerulonephritis
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| *Focal segmental glomerulosclerosis
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| *Membranous glomerulopathy
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| *Minimal-change disease
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| *Thin basement membrane disease
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| |-
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| | bgcolor="#ececec"|'''Secondary Disorder''' ||
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| *Lupus nephritis
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| *Post-infectious glomerulonephritis
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| *Glomerulonephritis related to hepatitis B or C
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| *Systemic vasculitides
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| **Wegener's granulomatosis
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| **Polyarteritis nodosa
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| **Henoch-Schonlein purpura
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| **Idiopathic
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| *Diabetic nephropathy
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| *Amyloidosis
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| *Light-chain nephropathy
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| *Human immunodeficiency virus nephropathy
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| *Alport's syndrome
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| *Drug-induced glomerulopathies
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| |}
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| ==References==
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| {{reflist|2}}
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| {{WH}}
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| {{WS}}
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| [[Category:Needs content]]
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| [[Category:Disease]]
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| [[Category:Nephrology]]
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| [[Category:Syndromes]]
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| [[Category:Pediatrics]]
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