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Credit to PeaceLuvHappiness on Quizlet, ive refined the notes to represent our content this year
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WBC
Mostly neutrophils

squamous epithelial cell
Folded skirt
Small nucleus, large cell
Lines urethra

transitional epithelial cell
Lines bladder, ureters
Smaller than squamous

Renal tubular epithelial cells
Circular
Confirm with lipid stain

oval fat body
Many bulbs
Confirmed with lipid stains

Bacteria
You may see them swimming or splitting

Yeasts
Most common for UTI is Candida albicans
Will not be lysed by acetic acid

Sperm
Oval head with thin long tail

Trichomonas
Usually in vaginal infection STI
Appears in white cells
Motion of organism is required to make ID

Enterobuis vermicularis
Worm looking organism
Larva will appear dark with a shell

Hyaline cast
Pure uromodulin
Parallel sides with rounded caps

RBC cast
Caused by trauma

WBC cast
Sign that issue is within the kidneys

RTE cast
Associated with drug toxicity

Mixed cell cast
Mix of cells in a cast

Fatty cast
Highly refractive cast with fats

Granular cast
composed of cellular remnants and byproducts of degradation

Waxy cast
Smooth, cylindrical, highly retractile
Sign of kidney failure

Broad cast
Thick, wide cast
Associated with end stage renal disease

Amorphous urates
Acidic urine
Granules

(C)
Calcium oxalate
Acidic to neutral urine
Has envelop, dumbbell and oval form
Associated with kidney stones and antifreeze ingestion

uric acid crystals
Acidic urine
Wedges
Can be in patients undergoing chemo

ammonium biurate crystal
Basic urine
“Thorny apple”
Old specimens

calcium phosphate crystals
Rare

leucine crystal
Yellow concentric circles
Liver disorder

triple phosphate crystal
Highly basic urine
Square
Associated with urease positive bacteria

bilirubin crystal
Acidic urine
Clumped needle
Associated with liver issues

cholesterol crystals
Associated with nephrotic syndrome
Refracts and shows bright cut crystals
Seen with fatty casts

cystine crystal
Hexagonal plates
Associated with inherited disorders
Children with kidney stones

tyrosine crystals
Needle
Liver disease

Mucous thread
Made by uromodulin that hasn't formed into casts

Air bubble
Artifact

Fiber
Artifact
Longer than any cast

starch
Artifact from powdered gloves

Fat
artifact
Confirm with Sudan stain
Acute kidney injury
Kidney suddenly stops filtering
Oliguria and anuria
Pre-renal
Reduced blood flow and high specific gravity
Inter-renal
Tubular necrosis
low specific gravity
Acute glomerulonephritis
Inflammation of glomerulus due to immune complex
Hematuria and proteinuria
Chronic glomerulonephritis
Loss of nephron mass
Moderate hematuria, proteinuria
Nephrotic syndrome
Glomerulonephritis consequence
Proteinuria
Oval fat bodies or RTEs
Membraneous nephropathy
Deposition of immune complexes causing thickening of glomerular basement membrane
Looks similar to glomerulonephritis
Minimal change disease
Nephrotic syndrome in children
T cell dysfunction leads to podocyte injury and infection
Acute tubular necrosis
Damage to renal tubules from toxins or low oxygen
Moderate proteinuria
RBCs, RTEs, RTE casts, granular casts
Renal tubular acidosis
Inability to produce acidic urine
Basic urine
Metabolic acidosis
Fanconi syndrome
Generalized defect in proximal tubule impairing reabsorption
Can be genetic or acquired
Impaired growth
Glucosuria, Aminoaciduria
Acute interstitial nephritis
Inflammation of renal interstitial via adverse reaction to drug therapy
Oliguria
WBC and WBC casts in urine
Renal calculi
Kidney stones
Calcium oxalate
Triple phosphate
Ammonium phosphate
Chronic kidney disease
Kidney damage for >3 months
Anuria, oliguria
High urinary protein
Waxy casts, broad casts
Jaundice
increased bilirubin in blood
Pre-hepatic, negative urine bilirubin
Haptoceullarl, negative to 1+ urine bilirubin
Post-hepatic, 3+ to 4+
UTIs
Typically caused by E. coli (can be Kleb, Prot, Entero)
Cystitis, in bladder
Increased pH, WBCs, possible nitrite
Urethritis, in urethra
Increased pH, WBCs, possible nitrite
Pyelonephritis, in kidneys
WBC casts, possible nitrite
Diabates mellatus
Metabolic disorder, cannot absorb glucose
Glucose, possible ketones in urine
Diabetes insipidus
Metabolic disorder, endocrine issues
Up to 20L of urine per day
Clear, colorless urine
Galactosemia
Inability to metabolize galactose due to deficiency of galactokinase
Jaundice, vomiting, slow baby growth
AMinoacidopathies
INherited enzyme defect involved in the metabolic pathway or transport of amino acids
Alkaptonuria
Autosomal recessive defiency, unable to degrade tyrosine
Urine darkening overtime
Maple syrup urine disease
Autosomal recessive deficiency
Sweet smelling urine
Slow baby growth
Melanuria
Dark colored urine due to presence of melanin
Associated with metastatic melanoma
Amyloidosis
Build up of amyloid proteins
Proteinuria
Porphyria
MEtabolic disorder associated with dysfunctional enzymes in heme biosyntheses pathways
Port wine urine