Picmonic: Renal Path Flashcards
1
Q
A
Post-Strep Glomerulonephritis
- Nephritic
- Group A strep pyogenes
- Neutrophil hypercellularity
- IF: granular
- EML subepithelial immune complex humps
- Children
- Edema of face/extremities
2
Q
A
Rapidly Progressive Glomerulonephritis
- Nephritic
- Crescents: contain fibrin and C3b
- Macrophages
- Caused by Goodpasture, Wegener’s, MicroPolyang.
- poor prognosis :(
3
Q
A
Diabetic Glomerulonephropathy
- Non-enzymatic glycosylation of BM & arterioles causes hyaline arteriosclerosis
- Increased GFR
- Mesangial expansion (From hyperfiltration)
- Type IV collagen deposition
- Neprhotic-like syndrome
4
Q
A
Focal Segmental Glomerulosclerosis
- MCC Adult Nephrotic Syndrome
- Associated with HIV & IV drug use
- LM: Segmental sclerosis + hyanlinosis
EM: Focal damage of visceral epithelial cells
IF: - - Microscopic hematuria; non-selective proteinuria
- Poor prognosis
5
Q
A
Bergers Disease / IgA Glomerulopathy
- MCC Nephritic Syndrome in children
- IgA deposits on mesangium, increased IgA plasma levels
- Also seen in Henoch-Scholein Purpura
- S/S: Pharyngitis, URI, Acute Gastroenteritis
6
Q
A
Membranoproliferative Glomerulonephritis
TYPE 1 MPGN:
- Subendothelial immune complexes (Hep C antibodies)
- IF: granular
- EM: double contour split BM due to ingrowth of mesangium
TYPE 2 MPGN:
- Dense Deposit Disease
- Circulating C3 Nephritic Factor
7
Q
A
Membranous Glomerulonephritis
- 2nd MCC Adult Nephrotic Synd (after FSGN)
- LM: Thickening of capillary and glomerular BM
EM: spikes & dome appearance + subendothelial deposits
IF: Granular - Sometimes assoc w/ gold, tumors, HBV, lupus
8
Q
A
Minimal Change Disease
- MCC Child Nephrotic Syndrome
- EM: loss of foot processes
LM: NORMAL - Loss of negative charge –> selective loss of albumin
- Maybe triggered by recent infx or immune stimulus
- Tx: corticosteroids
9
Q
A
Nephritic Syndrome
- Inflammation of glomeruli
- Hematuria
- RBC casts (intrarenal)
- Azotemia (nitrogen increased)
- Oliguria
- HTN
- Proteinuria (<3.5g/day)
10
Q
A
Nephrotic Syndrome
- Massive proteinuria (>3.5g/day)
- Edema
- increased risk of infection
- Thromboembolus
- Hyperlipidemia
- Fatty Casts
11
Q
A
Alport Syndrome
- Genetic Nephritic Syndrome
- XD mutation in Type IV Collagen
- Split basement membrane (in kidneys, eyes, ears)
- Ocular Disorders & Deafness also seen