Urinary pathology Flashcards
Pyelonephritis
Inflammation/infection of the renal cortex and interstitium
Possible dysuria and frequency
Fever and chills, N/V, flank pain, CVA tenderness
Chronic pyelonephritis assoc w/ recurrent acute pyelonephritis, kidney stones, or vesicoureteral reflux
Thyroidization of kidney – tubules fill w/ eosinophilic casts resembling colloid
Simple vs complex renal cysts
Simple: fluid filled asx inconsequential peripheral
Complex: solid component separations serial imaging needed surgical removal
Autosomal dominant polycystic kidney disease (ADPKD)
presents in adulthood
PKD1 on Chr 16 or PKD2 on Chr 4
numbers b/l renal cysts with massive enlargement of the kidney
HTN
progressive renal insufficiency -> ESRD
hemorrhage into cysts -> flank pain +/- hematuria
increased risk of kidney stones and UTI
Assoc w/ hepatic cysts, intracranial aneurysm, mitral valve prolapse
Autosomal recessive polycystic kidney disease (ARPKD)
PKHD1 on Chr 6
Presents in infancy or dx on prenatal u/s
b/l renal cysts, enlarged and echogenic kidneys
Oliguria -> oligohydramnios -> Potter sequence
HTN, renal insufficiency, hepatomegaly
Autosomal dominant tubulointerstitial kidney disease (aka medullary cystic kidney disease)
AD
small, shrunken kidneys and interstitial fibrosis
rarely produces cysts in renal medulla
progressive renal failure
Calcium oxalate stones
MC
hypercalcinuria hyperoxaluria -ethylene glycol ingestion -crohn's dz hypocitraturia Vit C ingestion
Radioopaque on XR
Envelope shape
Prevent w/ thiazine diuretics
Struvite stones (NH4MgPO4)
urease-positive bacteria
- proteus mirabilis pH >8
- Klebsiella
- S. saprophyticus
Radiopaque staghorn calculi
coffin lid shape
eradicate infection to prevent
Cystine stones
hereditary impairment of cystine reabsorption -> cystinuria
presents in childhood
Radiolucent staghorn calculi
hexagon shape
aklalinize urine to prevent
uric acid stones
hyperuricemia and gout
radiolucent
rhombus or rosette shape
allopurinol prevention
Renal cell carcinoma
MC primary renal malignancy
arise from PCT in the cortex
Risfactors:
mean 50-70, smoking, obesity, htn
deletion on Chr 3
-sporadic or part of von Hippel-Lindau disease
often asx, incidental finding
classic triad: flank pain, hematuria, palpable abdominal mass
-less than 10% of cases
paraneoplastic syndromes: polycythemia, anemia, hypercalcemia
Solid tumor w/ “clear cells” full of lipids/carbohydrates
Renal ocnocytoma
benign
densely packed eosinophilic cells
-nests
Wilms tumor (nephroblastoma)
MC renal malignancy of early childhood 2-4 yo
palpable abdominal/flank mass
possible abd pain or hematuria
WT1 or WT2 mutation on Chr 11
WAGR complex: wilms tumor aniridia genitourinary malformations - cryptochidism, bicornate uterus mental Retardation
transitional cell carcinoma (urothelial carcinoma)
MC malignancy of the urinary tract
Occur in Renal calyces or pelvis, ureters, and urinary bladder
Painless hematuria
Major risk factors: Smoking Aniline dyes Naphthylamine dyes cyclophosphamide
Squamous cell carcinoma of bladder
Smoking
chronic or recurrent UTIs
bladder stones
cyclophosphamide
Chronic irritation -> metaplasia -> dysplasia -> carcinoma
Schistosoma haematobium
Middle East