Renal Path Flashcards
Light chain casts seen in
Multiple myeloma nephropathy
Nephrotic vs nephrotic syndrome
Nephritic:
Inflamm
RBC casts
Nephrotic:
prOteinuria
Fatty casts
MCC acute nephritis children
PSGN
Hx: strep infection
Sub-epith humps on eMx
PSGN
Granular deposits w/in mensagium n glom capillary wall
PSGN
- starry sky / lumpy bumpy app
- IgG, IgM + C3 dep along GBM and mesangium
Acute kidney injury indications for dialysis
AEIOU
Acidosis Electrolytes: inc K+ Intoxication (SLIME : Salicylates, lithium, isopropanol, methanol, ethylene glycol) volume Overload Uremia
IF starry sky/ lumpy bumpy
Acute PSGN
IgG, IgM, C3
Linear IF
Goodpasture
Granular IF
- PSGN
- DPGN
- Lupus nephritis - wire looping
- MPGN - subendoth IC deposits (+ intramemb/ dense deposits) - TRAM TRACK APP
Basket weave IF
Alport syndrome
- Type IV collagen mutation
- “can’t see, can’t pee, can’t hear a bee”
EM - effacement ofnfoot processes
MCD + FSGN
EM : Spike and dome subepith deposits
Membranous nephropathy
- PSGN (starry sky/ lumpy bumpy)
Fibrocystin gene mutation seen in
ARPKD
PKHD1 gene
MCC Prerenal azotemia
Ischemia - hypovolemia
Epithelial / granular casts seen in
ATN
Muddy brown granular casts
MCC postrenal azotemia
B/l outflow obstruction d/t
- stones
- BPH
- Cong anomalies or neoplasm
MCC + location of ATN
- Ischemia
- Nephrotoxicity
PCT and ThAL
MCC Renal papillary necrosis
Infection or immune trauma
Other causes:
» POSTCARDS «
Pyelonephritis Obstruction of urinary tract SCA Tb Cirrhosis/ chronic alcohol Analgesic abuse Radiation / Renal transplant rejection Diabetes Systemic vasculitis
MCC CRF
Diabetic nephropathy
MCC Diabetic nephropathy
Loss of heparan sulfate forming the -ve charged filtration barrier, causing inc filtration of -ve charged serum proteins into the urine, predominately albumin
Abx to phospholipase A2 receptor seen in
Membranous nephropathy, Nephrotic
- spike and dome app on EMx
MCC u/l flank mass in children
Wilms tumor
- loss of (f) mutation in WT1 or 2 gene on chrom 11
- WAGR complex
- Denys-Drash syndrome
- Beckwith-Wiedmann syndrome
MCC u/l flank mass in children
Wilms tumor
- loss of (f) mutation in WT1 or 2 gene on chrom 11
- WAGR complex
- Denys-Drash syndrome
- Beckwith-Wiedmann syndrome
HTN w Berry aneurysm and MVP seen w?
ADPKD