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Nephritic Syndromes Dr. Raid Jastania.

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Presentation on theme: "Nephritic Syndromes Dr. Raid Jastania."— Presentation transcript:

1 Nephritic Syndromes Dr. Raid Jastania

2 Nephritic Syndrome Diffuse Proliferative (post infectious) GN
Rapidly Progressive GN (Crescentic GN) IgA Nephropathy Chronic Glomerulonephritis

3 Acute Proliferative/Diffuse Proliferative/Post-infectious Glomerulonephritis
Post strep (staph, measles, mumps, HepB, HepC) Immune complex

4 Acute Proliferative/Diffuse Proliferative/Post-infectious Glomerulonephritis
Light microscopy

5 Acute Proliferative/Diffuse Proliferative/Post-infectious Glomerulonephritis
Light microscopy: Proliferative: mesangial, endothelial, inflammation (neutrophils) Thrombi necrosis

6 Acute Proliferative/Diffuse Proliferative/Post-infectious Glomerulonephritis
Electron microscopy:

7 Acute Proliferative/Diffuse Proliferative/Post-infectious Glomerulonephritis
Electron microscopy: Sub-epithelial humps Other deposits

8 Acute Proliferative/Diffuse Proliferative/Post-infectious Glomerulonephritis
Immuno Fluorescence: Ig, Comp

9 Acute Proliferative/Diffuse Proliferative/Post-infectious Glomerulonephritis
Prognosis

10 Acute Proliferative/Diffuse Proliferative/Post-infectious Glomerulonephritis
Prognosis: Progression is uncommon 15-50% may progress to CRF

11 Rapidly Progressive GN (Crescentic GN)

12

13 Rapidly Progressive GN (Crescentic GN)
Type I: Anti GBM 12% LM: Crescent IF: Linear deposits, IgG, C3 EM: deposits, GBM rupture

14 Rapidly Progressive GN (Crescentic GN)
Type II: Immune complex 44% Post strep, IgA nephropathy LM: crescent IF: deposits similar to the primary disease EM: deposits, GBM rupture

15 Rapidly Progressive GN (Crescentic GN)
Type III: Pauci-immune, ANCA positive 44% Vasculitis: Wegener granulomatosis, microscopic polyarteritis LM: crescent IF: neg EM: neg, GBM rupture

16 IgA Nephropathy

17 IgA nephropathy Children, young adults
Microscopic, gross hematuria, recurrent Loin pain Association: Henoch-Schonlein purpura, Celiac disease, Liver disease

18 IgA nephropathy Pathogenesis

19 IgA nephropathy Pathogenesis: Abnormal IgA production and clearance
High level of IgA Deposits of IgA Immune complex Activation of alternative complement system (C3 only)

20 IgA nephropathy Light micorscopy

21 IgA nephropathy Light microscopy: Normal or mesangial expansion

22 IgA nephropathy Immuno Fluorescence:

23 IgA nephropathy Immuno Fluorescence: IgA in mesangium

24 IgA nephropathy Electron microscopy

25 IgA nephropathy Electron microscopy: deposits

26 IgA nephropathy Prognosis:

27 IgA nephropathy Prognosis: 25-50% progress to CRF

28 Chronic Glomerulonephritis

29 Chronic Glomerulonphritis
Late stage of glomerular disease Found in end-stage renal disease/CRF Represent 30-50% of patients on hemodialysis Young and middle age

30 What are the possible causes of this appearance of the kidneys?

31 Describe the four compartments (glomeruli, tubules, interstitium, and vasculature)

32 Describe the abnormality

33 Chronic Glomerulonphritis
Gross: Contracted kidneys Atrophic with granular surface

34 Chronic Glomerulonphritis
Micro: Glomerular sclerosis/hyalinizaiton Interstitial fibrosis/inflammation Tubular atrophy Thick vessels (hypertension)


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