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Aubf Lec - Midterm

The document outlines the procedures and significance of macroscopic and microscopic examination of urine sediment, including specimen preparation, centrifugation, and the identification of various cellular elements, casts, crystals, and bacteria. It details the clinical implications of findings such as dysmorphic red blood cells, white blood cells, and the presence of casts, which can indicate various renal disorders. Additionally, it discusses specific conditions related to tubular and interstitial disorders, as well as renal failure and lithiasis.

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Sweet Monday SM
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0% found this document useful (0 votes)
12 views

Aubf Lec - Midterm

The document outlines the procedures and significance of macroscopic and microscopic examination of urine sediment, including specimen preparation, centrifugation, and the identification of various cellular elements, casts, crystals, and bacteria. It details the clinical implications of findings such as dysmorphic red blood cells, white blood cells, and the presence of casts, which can indicate various renal disorders. Additionally, it discusses specific conditions related to tubular and interstitial disorders, as well as renal failure and lithiasis.

Uploaded by

Sweet Monday SM
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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AUBF LEC

Macroscopic Screening

❑ Specimen Preparation
❑ Specimen Volume
❑ Centrifugation
o RCF = 1.118 x 10-5 x radius in cm x
rpm
o Calibration
❑ Sediment Preparation
Urine Sediment Constituents
o 0.5 mL to 1.0 mL (after decantation)
o Resuspension by gentle agitation ▪︎ Cellular Elements
▪︎ Crystals
❑ Volume of Sediment Examined ▪︎ Cast
▪ 20 uL or 0.02mL
❑ Examining the Sediment Cellular Elements
▪ 10 fields both LPO (10x) and HPO Red Blood Cells (RBCs)
(40x)
➢ smooth, non-nucleated,
▪ Sediments examined under reduced
biconcave disks
light
➢ 7 mm in diameter
❑ Reporting the microscopic
examination ➢ Identified in HPO
▪ Cast – average # /lpf ➢ Average # in 10 hpf
▪ RBCs, WBCs – average # /hpf ➢ NV: 0-2/hpf
▪ Other elements – rare, few,
moderate, many
1+, 2+, 3+, 4+

Sediment Examination

❑ Sediment Stains
▪ Sternheimer-Malbin stain (crystal violet,
safranin O)
▪ WBCs,
▪ Epithelial cells
▪ cast
▪ 0.5% solution of toluidine blue
▪ WBC and RTE/RTC differentiation
▪ Cells from other body fluids
❑ Microscopy
▪ Bright-field microscopy (common)
Clinical Significance:
➢ Dysmorphic RBCs : glomerular
bleeding
➢ Damage of glomerular membrane
➢ Vascular injury within Genitourinary
tract
➢ Macroscopic Hematuria
▪ Advance Glomerular damage Mononuclear Cell
▪ Trauma ➢ Smaller numbers
➢ Lymphocytes : early sign of renal
▪ Acute infection/inflammation
rejection
▪ Coagulation disorder
➢ Monocytes, macrophages, and
histiocytes - large cells
White Blood Cells (WBCs) vacuolated or contain
➢ 12mm in diameter inclusions
➢ predominant: neutrophil – contains
granules and multilobed nuclei
➢ Identified in HPO
➢ Average # in 10 hpf
➢ NV: 0-5/hpf

Eosinophil
➢ Drug induced interstitial nephritis
➢ Not normally seen, 1% considered
significant
White Blood Cells (WBCs): Pyuria
➢ Hansel stain
➢ Predominantly seen
➢ contains granules and
multilobe nuclei
➢ Neutrophils: “glitter
cells” sparkling
appearance
Neutrophils
Epithelial Cells ➢ moderate cytoplasm
➢ normal sloughing of old cells ➢ Nucleus: 8-14 um, centrally located
➢ derived from the linings of ➢ Nucleus round or oval, off center in
genitourinary system elongated cells
➢ Viewed in LPO
➢ Semiquantitative in 10 lpf
➢ Squamous, Transitional, Renal

Squamous Epithelial cells:


➢ 40-60 um
➢ Shape : thin, irregular agled
(flagstone shape)
➢ Distinct boarder
➢ Abundant cytoplasm
➢ Nucleus: 8-14 um, centrally located
➢ Nucleus can be anucleated or
multinucleated Renal Tubular Epithelial cells
➢ Site: Small Collecting duct cells
➢ Shapes :
• 12-20um
• Polygonal or cuboidal
• Nucleus : larger covers 60-70%
of the cell
➢ Site: Large Collecting duct cells
• 6-10 um
• Shape: columnar
• Nucleus – 6-8 um off center

Transitional Epithelial cells


➢ 15-40 um
➢ Shapes : ➢ Site: DCT
• Round or pear shape ➢ Shapes :
• Clublike, caudate (with tail), • 14-25 um
elongated • Oval to round
• Small rectangular or columnar • Cytoplasm: grainy
like
• Nucleus: small, round central or
off center

➢ Site: PCT
➢ Shapes : Yeast
• 20-60um ➢ Refractile oval
• Oblong or cigar shape with ➢ Budding or no budding
indistinct cell ➢ Mycelial forms : branched
• Cytoplasm: grainy ➢ Viewed in HPO
• Nucleus: off center and ➢ Reported as rare, few, moderate, many
multinucleated ➢ Candida albicans : primary yeast
• Diabetic patients
• Immunocompromised patients
• Vaginal moniliasis (women)

Bacteria
➢ Cocci (spherical)
➢ Bacilli (rods)
• Viewed in HPO
• Reported as few. , moderate, many
• Motile bacteria suggestive of (+) culture
• Presence of bacteria can indicate LUTI or
UUTI

Parasites
➢ Trichomonas vaginalis (trophozoite)
• Pear shape flagellate Hyaline Cast
➢ Rapid fliting motion ➢ colorless
➢ Mycelial forms : branched ➢ Refractive index similar to urine
➢ Viewed in HPO (reduce light)
➢ Reported as rare, few, ➢ Shape:
moderate , many • normal parallel sides and
rounded ends
• cylindroid forms
• wrinkled or convoluted

Mucus
➢ Protein material
➢ Thread-like structures
➢ Viewed in LPO
RBC Cast
➢ Reported as rare, few,
➢ Indicates bleeding within the
moderate, many
nephron: glomerulonephritis
➢ orange-red color
➢ Reported:
• Average # 10 lpf

Cast
➢ Only element found in urinary sediment
of kidney WBC Cast
➢ Formed in lumens of DCT and collecting ➢ Infection within the nephron
ducts ➢ Pyelonephritis
➢ Viewed in LPO (HPO: further ➢ Composed of neutrophils
identification) ➢ Granular, multilobed nuclei
➢ Reported: average # 10 lpf ➢ Reported:
➢ Observation: subdued light, cast matrix • Average # 10 lpf
has low
refractive index
➢ Major Constituent of cast is Uromodulin
Epithelial cell Cast
➢ RTE cells
➢ Cells in the matrix Waxy Cast
• Smaller round ➢ Appearance
• Oval cells • Ground glass (brittle)
➢ Reported: • High refractive
• Average # 10 lpf • Homogeneous matrix
➢ Indicates chronic renal failure

Granular Cast
Fatty Cast
➢ Fine Granular Cast
➢ Appearance
• Small granules dispensed
• Fat droplets/oval fat bodies
throughout the matrix
• High refractile
• Sand Paper appearance
• Yellowish to green sheen
➢ Coarse Granular Cast
➢ Associated with nephrotic
• Larger coarse granules
syndrome
• Granules primarily from
degenerating cells
CRYSTALS
➢ Used to help diagnose kidney stones
➢ Problem in metabolism
➢ Formed:
• Precipitation of urinary solutes happen
due to
• Temperature
• Solute concentration
• pH
➢ Viewed on LPO
➢ Reported: rare, few, moderate, or
many

Normal Urine Crystals


Abnormal Urine Crystals
Bilirubin
▪ Yellow clumped needles or granules
▪ hepatic disorders
▪ Positive Chemical test result for bilirubin

Crystals Associated with Liver Disorder


▪︎ Tyrosine
▪︎ Leucine
▪︎ Bilirubin

Tyrosine
▪ fine colorless to yellow needles
▪ Seen together with leucine
▪ Positive chemical test for bilirubin
▪ Amino Acid metabolism disorder

Leucine
▪ yellow-brown spheres
▪ Seen together with tyrosine
▪ concentric circles and radial striations
Tubular Disorder Renal Glycosuria
▪︎ Tubules are disrupted ▪︎ Affects the reabsorption of glucose
▪︎ Caused by:
Acute Tubular Necrosis (ATN) -​ Decrease in the number of glucose
▪︎ Primary disorder transporters in tubules
-​ Decrease in the affinity of
▪︎ Categorized: Ischemic ATN, Toxic ATN transporters for gluvose
▪︎ Disorders leading to ATN include; shock, ▪︎ Inherited as an autosomal recessive trait
trauma, surgical procedure ▪︎ Correlation
▪︎ Correlation: mild proteinuria, microscopic
hematuria, RTE Renal Tubular Acidosis
▪︎ Characterized by the inability of the
Hereditary and Metabolic Tubular tubules
Disorder

Fanconi Syndrome INTERSTITIAL DISORDER


▪︎ Most frequently associated with tubular ▪︎ Most common renal disease - UTI
dysfunction -​ Lower UTI (urethra and bladder)
▪︎ Caused by generalized failure of tubular ▪︎ Urethritis: infection in the urethra
▪︎ may be inherited in association with ▪︎
cystinosis and Harrnup disease
▪︎ Correlation:
Alport Syndrome -​ Presence of numerous WBC
▪︎ Inherited disorder of collagen production
affecting basement membrane
-​ Can be Acute Pyelonephritis
▪︎ glomerular basement membrane exhibits ▪︎ Infection of the upper UT
lamellated -​ Ascending movement of bacteria
from lower UTI
Uromodulin-Associated Kidney Disease -​ Enhanced in the following
▪︎ inherited disorder caused by an autosomal conditions:
mutation in the gene ▪︎
▪︎ Tubules become necrotic
▪︎ correlation; increase in serum acid, ▪︎ Abcess formation from bacteria and
leukocytic enzymes
Diabetic Nephropathy ▪︎ Correlation:
▪︎ Most common cause of wnd stage renal -​ Numerous leukocytes
disease
▪︎Glomerular membrane is damaged by:
-​ Glomerular membrane thickening Chronic Pyelonephritis
▪︎ Develops when persistent inflammation or
Nephrogenic Diabetes insipidus renal
▪︎ Action ADH is disrupted by inability of the ▪︎ Results to permanent renal tubule damage
renal tubules to respond to ADH that leads to chronic renal failure
▪︎ Correlation:
-​ Increased leukocytes but bacteria
may or may not be present
-​ A

Acute Interstitial Nephritis


▪︎ Marked by inflammation
▪︎ commonly caused by acute allograft
rejection of transplant kidney
▪︎ Any immune response in the interstitium of
the kidney can cause AIN

▪︎ Correlation:
-​ Macroscopic hematuria
-​ Mild to moderate proteinuria
-​ Numerous WBCs
-​ WBC casts without bacteria

Renal Failure
▪︎ Acute Renal Failure
-​ Frequently reversible once patient is
treated correctly
-​ Correlation:

▪︎ Chronic Renal Failure


-​ Progressive

Renal Lithiasis
▪︎ Layman's term: kidney stones
▪︎ Can also be term as renal calculi
-​ Aggregates of solid chemical
▪︎ rarely composed of a single components
are mixture of
-​ A
▪︎ Factors influence calculi formation
-​ Supersaturation of chemical salts in
urine
-​ Optimal Urinary pH
-​ Urinary stasis
-​ Nucleation or initial crystal formation

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