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41 Cards in this Set

  • Front
  • Back
what's most common and best prognosis of HUS? and cause
D + HUS: E.coli
anemia, hemolysis, leukocytosis (30-40K) thrombocytopenia
-irritable, CNS dysfxn; pale, fussy, sz; coma;
-what GI sx?
HUS;
-/+ diarrhea: bloody, mucoid; colonic involvement (leukodcytosis); rectal prolapse, bowel necrosis
HUS tx?
dialysis for renal failure; No anbtx (worsens)
-transfuse for hct < 20;
-supportive care
?prevent HUS?
cook meat well; handwash; isolated infected pts
what makes good prognosis and poor prognosis of HUS?
D + ; good prognosis
- Poor prognosis: prolonged anuria (> 7 day)
-renal scarring on bx; and severe CNS involvement
3 yo fussy, pale, puffy; wBC 25/5/15/ plt 80; bmp: K 6.1, HCO 11; bun/cr: 40/3;
-dx? and tests?
HUS;
stool for E.coli;
-send coombs, (+ in pneumoccocal HUS)
-send C3, C4 - low in genetic causes of HUS)
defenine HTN in kids: what do you always check for ?
> 95th % for age and height
95% for SBP = (age x 3) + 100
95% for DBP (age x 1.5 ) + 70
-3 separate measurements;
Pre htn > 90%
most common cz of htn in kids?
renal causes, but also check for coarc;
1) parenchymal (Acute GN, scarring: UTI) vs
2) renovascular - narrowing of renal artery (renal artery stenosis, UAC, NF1 ~ cafe au lait - Neurfibromas pressing on renal artery)
infancy, HTN, what's most common form? ambiguous genitalia
CAH: 11 and 17: HTN;
most common 21; but doesn't cause HTN
goiter, taccy, flushing, HTN
hyperthyroidsm
striae, moon facies, buffalo hump, h/o steroid exposure
cushing's disease- overproduction of cortisol
teenage period, HTN:
drugs; need tox screen: + amphetamines, cocaine, PCP, cough/cold meds
NB most common htn?
RA or RV thrombosis
-RAS, Cong renal diz, coarc
HTN in 1st year life ?
coarc, renovasc diz, renal parenchymal diz
infancy-6 yo HTN causes?
renal parenchymal diz, renovas diz
Renal aretery stenosis, cafe aulait spots, pheochromocytoma ~ ?
Neurofibromatosis 1
sore throat, coca coala colored urine, HTN; ? Dx, tx?
PIAGN, diuretics
flugshin, sweating, HTN; dx/tx?
pheochromocytoma;
alpha beta blockade
recurrent UTI; dx/tx?
renal scarring; ACE
what condition is ACE I CI?
bilateral RAS
what is beta blockers and central alpha agonists CI?
depression
what is beta blockers CI?
asthma and diabetes
8 yo w/ BP 130/85, scoliosis, cafe au lati spots,
-cause, inheritance? ~
NF, AD, ~ pheochromcytoma
8 yo w/ bp 150/75; dark cola colored urine; h/o sore throat; cause/tx?
PIAGN; diuretics
14 yo w/ bp: 140/90?
check urine tox;
increased incidience of systemic diz (females)
when see > 10 WBC,
- when see no infex?
viral UTI, GN

-no infx: TB, appendicitis
urgency, frequency, dysuria, no Fevers, or systemic signs: ?
acute cystitis - inflamm of bladder mucosa
fever, flank pain, Vomiting,
infection of kidney: pyelo
what imaging do after dx UTI? whats most common complx > UTI?
1) upper tract: U/s (hydronephrosis)
-CT or IVP (

2) Lower tract: VCUG
- detects: VUR - most common complx (vesiculorenal reflux)
detects PUV
males, proteinuria, hematuria, deafness; ? inheritance
Alports;
-x-linked - defect w/ collagen IV; Kidney, eye, ear
young kid w/ light hair, skin presents w/ fanconi syndrome (which is what? )
cystinosis;
Fanconi syn: RTA, glucosiuria, phosphaturia ( but low serum phos) due to buildup of cystine chrystals --> renal failure/transplant
when liver can't break down oxalate
hyperoxaliuria, kidneys become 2 hard rocks: need liver and kidney transplant
most common renal tumor?
wilm's tumor
nephrotic syndrome, diffuse mesangial sclerosis, ambig genitalia;
-risk for wilm's and male psueduohermphrodism
drash syndrome
short, renal rickets: renal osteodystrophy;
HTN, anemia; Late electrolye disturbances
chronic kidney disease (CKD)
- (hyperkalemia - indication for dialysis)
dysplasia, U/L agenisis; branchial fistulas;
-kidney and ear problems, pits in ear/neck; hear loss
branchio-oto-renal syndrome
renal failure w/ oligo; small, post set ears, micrognathia, beaked nose, wide set eyes, pulm hypoplasia; small chin;
Potter's
dilated urinary tract, dysplastic, aplastic kidneys, hydronephrotic kidneys;
- no abd muscle, cyrptorchdoidism
prune belly
renal aplasia or hypoplasia, double colecting system; u/L aplasia of pec major w/ ipsalateral
?
renal agniomylipomas, cystic kidneys, renal cell ca.
-adenoma sebaciums, epilepsy, CNS tubers, retinal phakomas
Tuberous sclerosis
hematuria, protienuria, GN,
-lower limb - palpable purpura, abd pain, arthralgia;
-check for ? or ~ what GI d/o?
HSP; need to check for hematuria
-h/o arthralgia in Ext; GI involvement
-intussusc