Urinary pathology Flashcards

1
Q

Pyelonephritis

A

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

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2
Q

Simple vs complex renal cysts

A
Simple:
fluid filled
asx
inconsequential
peripheral
Complex:
solid component
separations
serial imaging needed
surgical removal
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3
Q

Autosomal dominant polycystic kidney disease (ADPKD)

A

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

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4
Q

Autosomal recessive polycystic kidney disease (ARPKD)

A

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

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5
Q

Autosomal dominant tubulointerstitial kidney disease (aka medullary cystic kidney disease)

A

AD

small, shrunken kidneys and interstitial fibrosis

rarely produces cysts in renal medulla

progressive renal failure

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6
Q

Calcium oxalate stones

A

MC

hypercalcinuria
hyperoxaluria
-ethylene glycol ingestion
-crohn's dz
hypocitraturia
Vit C ingestion

Radioopaque on XR

Envelope shape

Prevent w/ thiazine diuretics

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7
Q

Struvite stones (NH4MgPO4)

A

urease-positive bacteria

  • proteus mirabilis pH >8
  • Klebsiella
  • S. saprophyticus

Radiopaque staghorn calculi

coffin lid shape

eradicate infection to prevent

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8
Q

Cystine stones

A

hereditary impairment of cystine reabsorption -> cystinuria

presents in childhood

Radiolucent staghorn calculi

hexagon shape

aklalinize urine to prevent

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9
Q

uric acid stones

A

hyperuricemia and gout

radiolucent

rhombus or rosette shape

allopurinol prevention

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10
Q

Renal cell carcinoma

A

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

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11
Q

Renal ocnocytoma

A

benign

densely packed eosinophilic cells
-nests

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12
Q

Wilms tumor (nephroblastoma)

A

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
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13
Q

transitional cell carcinoma (urothelial carcinoma)

A

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
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14
Q

Squamous cell carcinoma of bladder

A

Smoking
chronic or recurrent UTIs
bladder stones
cyclophosphamide

Chronic irritation -> metaplasia -> dysplasia -> carcinoma

Schistosoma haematobium
Middle East

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