Renal Flashcards
Most common site of fetal obstruction
ureteropelvic junction
potters syndrome cause (limb/facial/pulmonary hypoplasia)
oligohydramnios
horseshoe kidney association
turner syndrome(under IMA)
clearance equation
UV/P
RBF equation
RPF/(1-Hct)
angiotensin II sites of action
efferent arteriole, ADH, NA-H exchange PCT(contraction alkalosis), AT1 vascular SM, aldosterone, hypothalamus
glucose clearance threshold
140
RAAS system sensors
JG cells=BP, macula densa=Na delivery
ANP mechanism
sense atrial pressure, relaxes SM via cGMP, Na loss
NSAIDs renal failure mechanism
inhibit prostaglandins that dilate afferent arteriole
anion gap
Na-(Cl+HCO3)>12, MUDPILES(normal=HARDASS)
fatty casts in urine
nephrotic syndrome
brown casts
tubular necrosis
waxy casts
chronic/advanced renal disease
nephrotic
proteinuria(>3.5), edema, fatty casts, hyperlipidemia
acetazolamide (CA inhibitor) use
altitude sickness/alkalosis/glaucoma
loop(furosemide/ethacrynic acid) toxicity
oto, low K, gout
thiazide MOA
Block DCT NaCl symporter
thiazide toxicity
hyperlipid/Ca/uric/glucose, low Na
Angiotensin II SE+mediator
dry cough& angioedema-bradykinin
polycystic kidney disease associations
hepatic fibrosis(autoRecessive), berry anyeurism(autoD)
Acute renal failure hallmark
azotemia, oliguria
BUN:Cr>15
pre& early post renal
BUN:Cr<15
tubular damage(late postrenal)
common renal tubular damage drugs
aminoglycosides, heavy metal, myoglobin, ethylene glycol
minimal change disease association
Hodgkins Lymphoma(cytokines)
minimal change disease pathology
effaced foot processes, selective proteinuria(not IG)
Focal segmental glomerulonephritis associations
HIV, heroin, sickle cell(nonresponsive to steroids MCD)
membranous associations
SLE, hepB&C, tumors, drugs
membranous pathology
subepithelial IC deposition-granular/spike and dome
membranoproliferative pathology
tram track(type I-subendothelial-hepB&C, II-basement membrane-C3 nephritic factor)
DM kidney pathology
NEglycosylation of basement membrane, hyaline arteriolosclerosis, kimmelstein wilson nodules
nephritic syndrome mediator
C5a neurophils
PostStrep GN pathology
hypercellular, IC lumpy bumpy
rapidly progressive pathology
fibrin+M0 crescents in bowmans space
specific rapidly progessive disease pathology
goodpasture-linear(+hemoptysis), pauci immune(no deposits), PSGN/diffuse proliferative(granular)
most common SLE renal association
diffuse proliferative GN(also membranous less likely)
pauci immune pathology
wegeners-cANCA+lung+nasopharynx, churg-strauss-pANCA/eosinophils/asthma/granulomas, microscopic polyangiitis-pANCA
Bergers pathology
mesangium IgA deposits, following mucosal infections
alport genes
X-linked type IV collagen, split basement membrane+deaf
UTI labs
WBCs, leukocyte esterase, nitrites
Vesicoureteral reflux findings
scarring inferior&superior poles
chronic pyelonephritis findings
waxy casts, proteinaceous follicles from atrophic tubules
most common stone
CaP/oxalate(crohns/hypercalcemia association)
AMP(struvite) pathology
urease+(proteus/klebsiella), staghorn, alkaline urine
uric acid stone pathology
radiolucent, gout, acidic(Tx alkalinize)
cysteine stone association
children, staghorn
EPO creation
renal peritubular interstitial cells
dialysis association
renal cell carcinoma
angiomyolipoma association
tuberous sclerosis
renal cell carcinoma paraneoplastic syndromes
EPO, renin, PTHrP, ACTH excess
renal cell genetics
loss VHF tumor suppressor(higher IGF, VEGF, PDGF) von hippel lindau association, chromosome 3
most common tumor in kids+pathology
wilms-blastema cells(WT1 mutation)
most common lower UT tumor
urothelial carcinoma(bladder) SMOKING, flat or papillary
squamous cell lower UT associations
Schistosoma hematobium(Middle eastern male), chronic cystitis, long standing stone
adenocarcinoma association
urachal remnant(dome of bladder), exstrophy, cystitis