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Change in Urine Color (2
Change in Urine Color (2
Supervised by:
Prof. Dr. Nariman Fahmi Ahmed
Done by :
ﻋﻤﺎر ﺳﻌﺪ ﻋﻠﻲ رﺷﯿﺪ
ﻋﺒﺪ اﻟﺮﺣﻤﻦ وﻋﺪ ﻋﺒﺪ اﻟﺴﺘﺎر
ﺳﺎرة ﻣﺤﻤﺪ ﺟﺎﺳﻢ
ﺳﺎرة ﻋﺪﻧﺎن ﺣﺴﻦ
رﻧﺪ ھﯿﺜﻢ ﺣﺴﻦ
Case Scenario 1
An 8 months old male infant was admitted to the ER for sings of respiratory
distress, after rapid assessment and evaluation, with history provided by the
mother, he was diagnosed with methemoglobinemia.
The following day, the infant’s urine was abnormal in color and hemoglobin
levels were down to 9.3 g/dl.
I will ask you..
1. What color you think the urine of the infant changed to? And
why?
A 1 year old girl was admitted to the Hospital, for diarrhea. The onset of the disease
was five days prior to the admission with anorexia and diarrhea. On the second day
of illness, a stool culture was performed, which was positive for enter pathogenic
Escherichia coli. On the fourth day of illness, the patient presented with dark
colored stools.
Alert but irritable and ill appearing child with a normal body temperature
The child’s weight at admission into hospital was 8700 g. The skin was pale,
slightly decreased skin turgor pale buccal mucosa, soft fontanelle and capillary
refill time of three seconds
Heart and lung examination were normal, except for tachycardia the abdomen
was distended, no hepatosplenomegaly There were no signs of meningeal
irritation no peripheral edema either
Q/ What is the most likely diagnosis?
INTRODUCTION
• Regular urine color ranges from clear to yellow color.
• Urobilin or urochrome, which is a product of bilirubin
degradation, is the chemical primarily responsible for the yellow
color of urine.
• Urine colors can vary depending on what you eat.
• Causes include:
• haemolytic disease like G6pd , liver disorders like hepatitis C or post
hepatic obstruction , some urinary tract infections, sever muscle injury
• Or certain medications like acetaminophen, methyldopa, chloroquine
•
Green urine
Causes include:
Pseudomonas infection.
Vitamin B supplements.
Fluorescein used in tests
Methyl blue dye
familial benign hypercalcemia
Drugs such as cimetidine and phenol
Cloudy urine
Also referred as turbid or foamy urine
Causes include
Urinary tract infection
Kidney stones
Dehydration
Diabetes
Pregnancy
STDs
Red or pink urine
caused by:
certain foods, such as blackberries.
certain medications, such as rifampin and laxatives that contain
senna.
poisoning from lead or mercury, severe muscle injury and hematuria
Hematuria
Glomerular origin:
● Postinfectious glomerulonephritis
● (IgA) nephropathy
● Lupus nephritis
● Thin basement membrane disease
● Alport syndrome
● Hemolytic-uremic syndrome
Non-Glomerular origin:
● UTI
● Trauma
● Kidney stones
● Sickle cell disease
● Coagulopathy
● Tumors
● Anatomic abnormalities
WHOA!
APPROACH TO RED COLOR
URINE
HISTORY
Age:
• 2-5 years Wilms tumor.
• 5- 12 years PSGN.
Sex:
• Female > male as UTI > 1 year and SLE nephritis
• Male > female in infant < 1 year (especially if
uncircumcised).
• X linked as Alport syndrome.
Race:
• White as in idiopathic hypercalcemia.
• Black as in SCD.
CHARACTER OF URINE DISCOLORATION
Color of urine:
❑ Red or pink (lower UT origin), drugs as rifampicin, deferoxamine, foods , food dyes,..
❑ Tea- or cola-colored (renal or glomerular)
❑ Black as bile pigments
Amount of urine: Reduced in AGN, ARF
Clots in urine: Extraglomerular
Frequency: Dysuria, recent enuresis: UTI
Frothy urine: Suggests Proteinuria seen in Glomerular diseases
Timing of color change:
✓ Initial (urethral source)
✓ Constant (glomerular or renal source)
✓ Terminal (hemorrhagic cystitis)
Persistent or intermittent
ASSOCIATED SYMPTOMS
• Fever (suggests infectious or systemic illness)
• Loin pain (renal colic suggests a stone)
• Voiding symptoms: incontinence, dysuria, frequency, urgency,(suggest
hemorrhagic cystitis)
• Facial puffiness, Oedema of legs, weight gain, Shortness of breath: AGN
• Hypertension (Headache, visual changes, epistaxis, seizures): AGN, ARF
• Abdominal pain: Urolithiasis (Loin to groin), UTI, clots, Nutcracker syndrome
• Painless: Glomerular
• Abdominal mass: Hydronephrosis, PKD, Wilms tumor
• Joint pain (HSP, SLE)
• Rashes (HSP, SLE)
• Neurologic: SLE, HUS (seizures, irritability)
• Jaundice: Hemolysis, Obstructive jaundice
PAST HISTORY:
Family history:
• Hematuria, renal diseases, renal failure (may suggest hereditary nephritis)
• Renal stone, SLE, coagulation disorders.
• Premature deafness (Alports syndrome).
Social history:
• Child abuse
• Exposure to hepatitis b or c.
• Occupational exposure to toxins.
EXAMINATION
GENERAL APPEARANCE:
• Check for the level of consciousness
• Orthopneic position if there is renal impairment
• Pallor
Vitals:
• Vital measurement especially HR and blood pressure as in AGN
• Temperature for UTI and AGN
HEAD TO TOE EXAMINATION:
• Eye and ear problem for Alport syndrome
• Aniridia for Wilms tumor
• Check for periorbital and leg edema
HEAD TO TOE EXAMINATION:
• Joint for arthritis as in HSP and SLE
• Skin lesion for: Purpura (HSP), Butter fly rash (SLE)
ABDOMINAL EXAMINATION
• Renal mass as in hydronephrosis, PSK, or Wilms
tumor
• Examination for bladder distension
Investigations
1. Blood test
2. General urine examination
3. Dipstick test
4. Microscopic examination
LINES OF TREATMENT
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THANK YOU