Pathology Glomerular Disease Flashcards
1
Q
Patterns of Immunofluorescent staining in Glomerular disease
A
- Linear (Type I RPGN, Diabetic)
- Granular (IgA; Membranous; SLE; C3 type)
- Irregular/fluffy: Amyloidosis
2
Q
Nephrotic syndrome S/S
A
- Massive proteinuria > 3.5
- Hyp[opalbuminemia
- Edema
- Hyperlipidemia
3
Q
Nephrotic Syndrome Pathogenesis
A
- Glomerular damage to podocytes/epithelium
- INC Permability leading to proteinuria/hypoproteinemia –> DEC plasma oncotic pressure -> DEC volume -> DEC GFR -> Edema
- Hypoproteinemia -> protein synthesis -> Hyperlipidemia
4
Q
Minimal Change Disease - Eti - Path - LabDx - A/S -
A
- Eti: Unknown; Immune trigger
- Path: Cytokines -> Podocyte effacement + INC glomerular permeability
- LabDx: Nothing on light Mx or IF; Effacement on Electron microscopy
- A/S: Hodgkins Lymphoma
5
Q
Focal Segmental Glomerulosclerosis
- Epi
- Path
- LabDx
- Genetics
- A/S
A
- EPI: AAs
- Path: Segmental obliteration of capillary w/ glomerular sclerosis due to matrix accumulation, adhesions, + hyalinosis
- LabDx: Focal/segmental consolidation; No immune complexes; effacement of podocytes
- Genetics: ACTN4 gene
- A/S: Obesity, SCD, Heoin use, Infx, loss of nephrons
6
Q
Membranous glomerulonephritis
- EPI:
- Path
- LabDx
A
- EPI: Asians
- Path: Deposits -> projections/spikes -> BM formation surround deposits -> irregular thick BM
- LabDx: Diffuse wall thickening; Subepithelial Immune deposits against PLA2R
7
Q
Membranoproliferative glomerulonephritis
- PAth
- LabDx:
A
- LabDx: Capillary wall thickensing w/ endocapillary hypercellularity; dense deposits (type II)
8
Q
FSGS Variants (5)
A
- Collapsing: Podocyte hypertrophy collapsing vesselks; C3 IF
- “Tip”: More likely to respond to steroids; herniation of tuft into Proximal tubule
- Cellular variant: segmental endocapillary hypercellularity;
- Perihilar: sclerosis localizes to perihilar segments within glomeruli + in deep cortical glomeruli
- NOS: random distribution of scarring