Renal III Flashcards

1
Q

RBC casts

A

glomerulonephritis

malignant HTN

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2
Q

muddy brown cysts

A

acute tubular necrosis

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3
Q

oval fat bodies

A

fatty cast

with nephrotic syndrome

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4
Q

waxy cast

A

end stage renal disease

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5
Q

focal

A
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6
Q

diffuse

A

> 50% glomeruli

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7
Q

nephritic syndromes

A
PSGN
RPGN
IgA nephropathy - berger
alport
MPGN
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8
Q

nephrotic syndromes

A
FSGS
minimal change disease
membranous nephropathy
amyloid
diabetic glomerulonephropathy
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9
Q

nephritic

A

GBM disruption

-inflammatory process

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10
Q

nephrotic

A

podocyte disruption

> 3.5 g/day

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11
Q

PSGN

A

strep pyogenes - group A strep infection
-type III hypersensitivity

starry sky - granular
lumpy bumpy IgG, IgM, C3

subepi IC deposits

resolve spontaneously

anti-DNase B titers and low complement

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12
Q

RPGN

A

crescentic

fibrin and plasma proteins (C3b)
poor prognosis

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13
Q

goodpasture

A

type II hypersensitivity
anti-GBM Abs - linear deposits

nephritic syndrome

progress - RPGN type I

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14
Q

granulomatosis with polyangiitis

A

wegener

PR3-ANCA

cANCA

can lead to RPGN

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15
Q

microscopic polyangiitis

A

MPO-ANCA

pANCA

can lead to RPGN

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16
Q

DPGN

A

with SLE or MPGN

wire looping caps
subendo and intramembrane IgG ICs

IF - granular

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17
Q

IgA nephropathy

A

berger disease

LM - mesangial proliferation
EM - mesangial IC deposits
IF - IgA IC deposits in mesangium

renal path of HSP

18
Q

alport syndrome

A

type IV collagen

thin and split BM

most common X-linked

get eye problems, glomerulonephritis, sensorineural deafness

19
Q

can’t see, can’t pee, can’t hear a buzzing bee

A

alport syndrome

get glomerulonephritis
retinopathy and lens dislocation

due to type IV collagen mutation

20
Q

MPGN

A

type I - subendo deposits - tram track
-association hep B and C

type II - intramembranous - dense deposits
-association C3 nephritic factor - stabilize C3 convertase

21
Q

FSGS

A

segmental sclerosis and hyalinosis

focal deposits IgM, C3, and C1

effacement of foot processes

in AAs and hispanics
HIV, sickle cell, heroin abuse, massive obesity, IFN tx

22
Q

liphoid nephrosis

A

minimal change disease

effacement of foot processes - electron microscopy

normal glomeruli on light microscopy and IF

in children
excellent response to corticosteroids

23
Q

membranous nephropathy

A

LM - diffuse cap and GBM thickening
IF - granular deposits IC
EM - spike and dome appearance - subepi deposits

poor response to steroids
may progress chronic renal disease

24
Q

kimmelstein wilson nodules

A

nonenzymatic glycosylation of GBM

pink diffuse mesangial deposition

25
ethylene glycol
oxalate crystals
26
coffin lid shape
ammonium Mg phosphate
27
struvite stone
ammonium Mg P -infection - urease positive bug hydrolyze urea to ammonium staghorn calculi stones - radiopaque
28
uric acid stones
precipitate at acid pH radiolucent - don't see on Xray tx alkaline urine and allopurinoll
29
calcium stone
Ca-P - precipitate at high pH | Ca-oxalate - precipitate at low pH
30
tx calcium stones
hydration thiazides citrate
31
hexagonal stone
cystine precipitate at low pH auto recessive -cystine reabsorbing PCT transporter lose function often in children can form staghorn
32
DDx cystine stone
sodium CN nitroprusside test
33
tx of cystine stone
low pH
34
elevated serum Cr with hydronephrosis
only if B/L or pt with one kidney
35
renal cell carcinoma
from PCT cells polygonal clear cells MC - men - 50-70yo MC primary renal malignancy with paraneoplastic syndromes - EPO, ACTH, PTHrP
36
renal cell carcinoma genetic
with VHL - chromosome 3
37
tx renal cell carcinoma
resection localized disease resistant to chemo or radiation
38
spread of renal cell carcinoma
invade renal vein - then IVC - spread hematogenous mets to lung and bone
39
renal oncocytoma
B9 - epithelial cell tumor large eisinophilic cell abundant mitochondria painless hematuria, flank pain, abdominal mass resect to exclude malignancy
40
wilms tumor
nephroblastoma MC renal malignancy early childhood - age 2-4 yo large palpable unilateral flank mass LOF mutation - WT1 or WT2 - CH 11
41
beckwith wiedemann syndrome
wilms macroglossia organomegaly hemihypertrophy
42
WAGR complex
wilms tumor aniridia GU malformation mental Retardation