Pathology Flashcards
Nephritic
Haematuria
Oliguria
Hypertension
Mild proteinuria
Nephrotic
Proteinuria
Hypoproteinaemia
Oedema
Immune-Mediated glomerular disease
Circulating immune complex deposit in glomerulus, entrap or deposit foreign antigen in BM leading to complement activation.
Acute Proliferative GN
Aet: Post Group A haemolytic strep infection
Morph: Glomeruli: enlarged, hypercellular, polymorphs, mesangial/endothelial proliferation
Clinic: low serum complement, high ASO tire
Result: chronic/crescentric GN
Crescentic GN
Proliferation of cells in capsular space
Stimulated by fibrin
Petechial hemorrhages
Aet: APGN, Autoimmune, SBE, Anti-BM disease
Morph: Glomeruli: necrosis, tufts collapse
Prog: Poor
RPGN
All idiopathic
Type 1 (anti-GBM antibody) Good pasture Syndrome
Type 2 (immune complex) Postonfectious, SLE, henoch-schonlain purpura
Type 3 (pauci-immune) ANCA, Wegener granulomatosis, polyarteritis nodosa
Minimal change nephropathy
Aet: idiopathic
Macro: large pale kidney
Micro: oedema in interstitium
Clinic: common in children
Prog: 75% recover
Focal segmental glomerulosclerosis
Causes
Primary FSGS HIVAN Heroin Drug toxicity Familial
HIV associated nephropathy
Collapsing variant of FSGS
Focal cystic dilation of tubules segments
->filled with: proteinaceous material, fibrosis, inflam
Large no. of tubuloreticular inclusions in endothelial cells.
Chronic GN
Aet: endstage of GNs
Micro: Glomeruli- hyalination, scarring, shrinkage
Tubule- atrophy, intervening hypertrophy
Interstitium- fibrosis, chronic inflam cells
Clinic: Chronic RF - Uraemia
Prog: RF,
Systemic diseases with glomerular involvement
SLE Diabetes Amyloidosis Good pasture Syndrome Bacterial endocarditis Henoch-schonlein purpura Wegener granulomatosis
Membranous GN
Aet: idiopathic, infection, neoplasms, autoimmune
Micro: Glomeruli-> uniform BM thickening
Tubules-> contain lipids
Institium-> fibrosis, foamy histicytes
Clinic: common in adults
Mesangiocapillary GN
Aet: post infection, autoimmune
Micro: Glomeruli-> very cellular-> lobularity
IgA Nephropathy
Glomerular IgA> intense or= staining to IgG/M
Asymptomatic haematuria(40%), gross haematuria(40%), Nephrotic syndrome(10%), renal failure(10%)
Histo: focal/diffuse Mesangioproliferative GN, endocapillary gn, crescentic gn
Diabetic Glomerulosclerosis
Kimmelstiel-Wilson kidney
Aet: longstanding diabetes
Macro: large smooth-> small granular kidneys
Micro:
Glomeruli-> nodular proteinaceous lesions, increase mesangial matrix, fibrin cap, hyalinization, shrinkage
Tubules-> atrophy, hypertrophy
B.vessels-> hypertensive e/a aterioles changes
Clinic: Nephrotic
Path: pyelonephritis, papillary necrosis