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1
DEFINITION
More than three red blood cells are found in
centrifuged urine per high-power field
microscopy
( > 3 RBC/HP).
Normal urine:
no red blood cell or less than three red blood
cell
2
According to the amount of RBC in the
urine, hematuria can be classified as:
 Microscopic hematuria:
normal colour with eyes
 Gross hematuria:
tea-colored, cola-colored, pink or
even red
3
ETIOLOGY
Diseases of the urinary system
I Vascular
Arteriovenous malformation
Arterial emboli or thrombosis
Arteriovenous fistula
Renal vein thrombosis
Loin-pain hematuria syndrome
Cogulation abnormality
Excessive anticogulation
4
ETIOLOGY
II Glomerular
IgA nehropathy
Thin basement membrane disease (incl.Alport syndrome)
Other causes of primary & secondary glomerulonephritis
III Interstitial
Allergic interstitial nephritis
Analgesic nephropathy
Renal cystic diseases
Acute pyelonephritis
Tuberculosis
Renal allograft rejection
5
ETIOLOGY
IV Uroepithelium
Malignancy
Vigorous exercise
Trauma
Papillary necrosis (common in DM and sickle cell trait/disease)
Cystitis/Urethritis/Prostatitis(usually caused by infection)
Parasitic diseases (e.g. schistosomiasis)
Nephrolithiasis or bladder calculi
V Multiple sites or source unknown
Hypercalciuria
Hyperuricosuria
6
ETIOLOGY
System disorders
a. Hematological disorders
Aplastic anemia Leukemia
Allergic purpura Hemophilia
ITP (idiopathy thrombocytopenic purpura)
b. Infection
Infective endocarditis
Septicemia
Epidemic hemorrhagic fever (Hantaan virus)
Scarlet fever (-hemolytic streptococcus)
Leptospirosis (leptospire)
Filariasis (Wuchereria bancrofti, Brugia malayi)
7
ETIOLOGY
c. Connective tissue diseases
Systemic lupus erythematosus (SLE)
Polyarteritis nodosa
d. Cariovascular diseases
Hypertensive nephropathy
Chronic heart failure
Renal artery sclerosis
e. Endocrine and metabolism diseases
Gout
Diabetes mellitus
8
ETIOLOGY
Diseases of adjacent organs to urinary tract
Appendicitis , Salpingitis
Carcinoma of the rectum
Carcinoma of the colon
Uterocervical cancer
Drug and chemical agents
Sulfanilamides, Anticogulants
Cyclophosphamide, Mannitol
Miscellaneous
Exercise, “idopathic” hematuria
9
CLINICAL FEATURES
 Color
depends on the amount of red blood cell in the
urine and the pH
normal: light yellow, pH 6.5
 pH
acidic: more darker (brown or black)
alkaline: red
10
DIFFERENTIAL DIAGNOSIS
 Contaminated urine: menstruation
 Drug and food: phenosulfonphthalein (PSP),uric
acid, vegetable
 Porphyrism: porphyrin in urine (+)
 Hemoglobinuria
11
LABORATORY TESTS
Three-glass test
Method: collecting the three stages of urine of
a patient during micturition
Result:
 the initial specimen containing RBC—the urethra
 the last specimen containing RBC—the bladder
neck and trianglar area, posturethra
 all the specimens containing RBC—upper urinary
tract, bladder
12
ACCOMPANIED SYMPTOMS
 Hematuria with renal colic
Renal stone, ureter stone
If with dysuria, micturation pause or straining to void:
bladder or urethral stone
 Hematuria with urinary frequency, urgency
and dysuria
Bladder or lower urinary tract (tuberculosis or tumor)
If accompanied by high spiking fever, chill and loin
pain: pyelonephritis
13
 Hematuria with edema and hypertension
glomerulonephritis
hypertensive nephropathy
 Hematuria with mass in the kidney
neoplasm
hereditary polycystic kidney
 Hematuria with hemorrhage in skin and
mucosa
hematological disorders
infectious diseases
 Hematuria with chyluria
filariasis
14
--Approaching to the patient–
(Harrison’s Principle of Internal
Medicine,14th Ed)
HEMATURIA
proteinuria (>500mg/24h)
Dysmorphic RBC or RBC casts
Pyuria,WBC casts urine culture
eosinophils serologic and hematologic
evaluation: blood culture,
anti-GBM Ab, ANCA,
complement, cryoglobulin
HBV,HCV,VDRL,HIV, ASLO
renal biopsy
Hb electrophoresis, urine cytology,
UA of family member, 24h urinary
calcium/uric acid
IVP+/-renal
ultrasound
As indicated:
retrograde
pyelography or
arteriogram of cyst
aspiration
cystoscopy
CT scan
biopsy
open renal biopsy
follow
(-)
(-)
(-)
(-)
(-)
(-)
(+)
(+)
(+)
(+)
(+)
ANCA:antineutrophil cytoplasmic
antibody, VDRL:venereal dis.
research laboratory, ASLO:
antisteptolysin O, IVP:
intravenous pyelography 15
Glomerular V/s Extraglomerular
bleeding
Urinary finding Glomerular Extraglomerular
Red cell casts May be present Absent
Red cell
morphology
Dysmorphic Uniform
Proteinuria May be present Absent
Clots Absent Absent
Color May be red or
brown
May be red
16
Renal causes of Hematuria
Glomerular
- Acute Postinfectious Glomerulonephritis
- IgA Nephropathy
- Hereditary Nephritis ( Alport syndrome)
- Benign Recurrent or Persistent Hematuria (Thin
Membrane Disease)
1.Sporadic
2.Familial
- Membranoproliferative Glomerulonephritis
- Crescentic Glomerulonephritis
- Lupus Nephritis
- Nephritis of Henoch-Shönlein Purpura
- Focal Glomerulosclerosis
- Hemolityc-Uremic Syndrome
17
Renal causes of Hematuria
Non-glomerular
- Infection ( Pyelonephritis )
- Interstitial Nephritis
- Metabolic ( Uric Acid, Nephrocalcinosis )
- Renal Malformation ( Cystic Kidney )
- Tumors ( Wilm’s, Acute Leukemia)
- Idiopatic Hypercalciuria
- Trauma
18
Causes of urinary tract related
Hematuria
Infection
Urolithiasis/Stone
Obstruction ( UPJ Stenosis )
Trauma
Drugs ( Cyclophosphamide )
Tumors/Neoplasm
19
Evaluation of Hematuria
History
Detailed review of family history
hematuria
proteinuria
renal insufficiency
stones
Precipitating factors
infection
exercise
Abdominal pain
hydronephrosis
pyelonephritis
urolithiasis
20
Evaluation of Hematuria
Physical Examination
Growth failure
Hypertension
Pallor
Edema
Rash
Abdomen: search for a mass or tenderness
External genitalia: bleeding
infection
trauma
21

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Amar_Jyoti_Hematuria.pptx

  • 1. 1
  • 2. DEFINITION More than three red blood cells are found in centrifuged urine per high-power field microscopy ( > 3 RBC/HP). Normal urine: no red blood cell or less than three red blood cell 2
  • 3. According to the amount of RBC in the urine, hematuria can be classified as:  Microscopic hematuria: normal colour with eyes  Gross hematuria: tea-colored, cola-colored, pink or even red 3
  • 4. ETIOLOGY Diseases of the urinary system I Vascular Arteriovenous malformation Arterial emboli or thrombosis Arteriovenous fistula Renal vein thrombosis Loin-pain hematuria syndrome Cogulation abnormality Excessive anticogulation 4
  • 5. ETIOLOGY II Glomerular IgA nehropathy Thin basement membrane disease (incl.Alport syndrome) Other causes of primary & secondary glomerulonephritis III Interstitial Allergic interstitial nephritis Analgesic nephropathy Renal cystic diseases Acute pyelonephritis Tuberculosis Renal allograft rejection 5
  • 6. ETIOLOGY IV Uroepithelium Malignancy Vigorous exercise Trauma Papillary necrosis (common in DM and sickle cell trait/disease) Cystitis/Urethritis/Prostatitis(usually caused by infection) Parasitic diseases (e.g. schistosomiasis) Nephrolithiasis or bladder calculi V Multiple sites or source unknown Hypercalciuria Hyperuricosuria 6
  • 7. ETIOLOGY System disorders a. Hematological disorders Aplastic anemia Leukemia Allergic purpura Hemophilia ITP (idiopathy thrombocytopenic purpura) b. Infection Infective endocarditis Septicemia Epidemic hemorrhagic fever (Hantaan virus) Scarlet fever (-hemolytic streptococcus) Leptospirosis (leptospire) Filariasis (Wuchereria bancrofti, Brugia malayi) 7
  • 8. ETIOLOGY c. Connective tissue diseases Systemic lupus erythematosus (SLE) Polyarteritis nodosa d. Cariovascular diseases Hypertensive nephropathy Chronic heart failure Renal artery sclerosis e. Endocrine and metabolism diseases Gout Diabetes mellitus 8
  • 9. ETIOLOGY Diseases of adjacent organs to urinary tract Appendicitis , Salpingitis Carcinoma of the rectum Carcinoma of the colon Uterocervical cancer Drug and chemical agents Sulfanilamides, Anticogulants Cyclophosphamide, Mannitol Miscellaneous Exercise, “idopathic” hematuria 9
  • 10. CLINICAL FEATURES  Color depends on the amount of red blood cell in the urine and the pH normal: light yellow, pH 6.5  pH acidic: more darker (brown or black) alkaline: red 10
  • 11. DIFFERENTIAL DIAGNOSIS  Contaminated urine: menstruation  Drug and food: phenosulfonphthalein (PSP),uric acid, vegetable  Porphyrism: porphyrin in urine (+)  Hemoglobinuria 11
  • 12. LABORATORY TESTS Three-glass test Method: collecting the three stages of urine of a patient during micturition Result:  the initial specimen containing RBC—the urethra  the last specimen containing RBC—the bladder neck and trianglar area, posturethra  all the specimens containing RBC—upper urinary tract, bladder 12
  • 13. ACCOMPANIED SYMPTOMS  Hematuria with renal colic Renal stone, ureter stone If with dysuria, micturation pause or straining to void: bladder or urethral stone  Hematuria with urinary frequency, urgency and dysuria Bladder or lower urinary tract (tuberculosis or tumor) If accompanied by high spiking fever, chill and loin pain: pyelonephritis 13
  • 14.  Hematuria with edema and hypertension glomerulonephritis hypertensive nephropathy  Hematuria with mass in the kidney neoplasm hereditary polycystic kidney  Hematuria with hemorrhage in skin and mucosa hematological disorders infectious diseases  Hematuria with chyluria filariasis 14
  • 15. --Approaching to the patient– (Harrison’s Principle of Internal Medicine,14th Ed) HEMATURIA proteinuria (>500mg/24h) Dysmorphic RBC or RBC casts Pyuria,WBC casts urine culture eosinophils serologic and hematologic evaluation: blood culture, anti-GBM Ab, ANCA, complement, cryoglobulin HBV,HCV,VDRL,HIV, ASLO renal biopsy Hb electrophoresis, urine cytology, UA of family member, 24h urinary calcium/uric acid IVP+/-renal ultrasound As indicated: retrograde pyelography or arteriogram of cyst aspiration cystoscopy CT scan biopsy open renal biopsy follow (-) (-) (-) (-) (-) (-) (+) (+) (+) (+) (+) ANCA:antineutrophil cytoplasmic antibody, VDRL:venereal dis. research laboratory, ASLO: antisteptolysin O, IVP: intravenous pyelography 15
  • 16. Glomerular V/s Extraglomerular bleeding Urinary finding Glomerular Extraglomerular Red cell casts May be present Absent Red cell morphology Dysmorphic Uniform Proteinuria May be present Absent Clots Absent Absent Color May be red or brown May be red 16
  • 17. Renal causes of Hematuria Glomerular - Acute Postinfectious Glomerulonephritis - IgA Nephropathy - Hereditary Nephritis ( Alport syndrome) - Benign Recurrent or Persistent Hematuria (Thin Membrane Disease) 1.Sporadic 2.Familial - Membranoproliferative Glomerulonephritis - Crescentic Glomerulonephritis - Lupus Nephritis - Nephritis of Henoch-Shönlein Purpura - Focal Glomerulosclerosis - Hemolityc-Uremic Syndrome 17
  • 18. Renal causes of Hematuria Non-glomerular - Infection ( Pyelonephritis ) - Interstitial Nephritis - Metabolic ( Uric Acid, Nephrocalcinosis ) - Renal Malformation ( Cystic Kidney ) - Tumors ( Wilm’s, Acute Leukemia) - Idiopatic Hypercalciuria - Trauma 18
  • 19. Causes of urinary tract related Hematuria Infection Urolithiasis/Stone Obstruction ( UPJ Stenosis ) Trauma Drugs ( Cyclophosphamide ) Tumors/Neoplasm 19
  • 20. Evaluation of Hematuria History Detailed review of family history hematuria proteinuria renal insufficiency stones Precipitating factors infection exercise Abdominal pain hydronephrosis pyelonephritis urolithiasis 20
  • 21. Evaluation of Hematuria Physical Examination Growth failure Hypertension Pallor Edema Rash Abdomen: search for a mass or tenderness External genitalia: bleeding infection trauma 21