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Alterations of Renal and Urinary Tract Function in Children

Alterations of Renal and Urinary Tract Function in Children. Chapter 30. Structural Abnormalities. Horseshoe kidney Hypospadias Chordee Epispadias Exstrophy of the bladder. Hypospadias. Structural Abnormalities. Bladder outlet obstruction Ureteropelvic junction obstruction (UPJ)

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Alterations of Renal and Urinary Tract Function in Children

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  1. Alterations of Renal and Urinary Tract Function in Children Chapter 30

  2. Structural Abnormalities • Horseshoe kidney • Hypospadias • Chordee • Epispadias • Exstrophy of the bladder

  3. Hypospadias

  4. Structural Abnormalities • Bladder outlet obstruction • Ureteropelvic junction obstruction (UPJ) • Secondary UPJ • Hypoplastic or dysplastic kidneys • Renal aplasia or dysplasia • Polycystic kidney disease • Renal agenesis • Unilateral or bilateral (Potter syndrome)

  5. Glomerular Disorders • Glomerulonephritis • Immunoglobulin A (IgA) nephropathy • Nephrotic syndrome • Hemolytic uremic syndrome

  6. Glomerulonephritis • Acute poststreptococcal glomerulonephritis • Occurs after a throat or skin infection with certain strains of group A alpha-hemolytic streptococci • Experience a sudden onset of hematuria, edema, hypertension, and renal insufficiency

  7. Glomerulonephritis • Acute poststreptococcal glomerulonephritis • Antigen-antibody complexes and complement are deposited in the glomerulus • The immune complexes initiate inflammation and glomerular injury

  8. Glomerulonephritis • Immunoglobulin A (IgA) nephropathy • IgA nephropathy is characterized by the deposition of mostly IgA but some IgM antibodies and complement in the mesangium of the glomerular capillaries

  9. Glomerulonephritis • Henoch-Schönlein purpura nephritis • Also referred to as anaphylactoid purpura • IgA nephropathy that causes inflammation and damage to the glomerular blood vessels

  10. Nephrotic Syndrome • Nephrotic syndrome is a symptom complex related to loss of protein in the urine • Minimal change nephropathy (MCN) • Focal segmental glomerulosclerosis (FSGS) • Congenital nephrotic syndrome • Nephrotic syndrome can be primary or secondary in relation to cause

  11. Hemolytic-Uremic Syndrome (HUS) • HUS is the most common cause of acute renal failure in children • There is an association of HUS with bacterial and viral agents • Escherichia coli 0157:H7

  12. Hemolytic-Uremic Syndrome (HUS) • The bacterial toxin from E. coli damages red cells and endothelial cells • The endothelial lining of the glomerulus becomes swollen and occluded with fibrin clots

  13. Hemolytic-Uremic Syndrome (HUS) • The damaged red cells are removed from the circulation by the spleen, causing acute hemolytic anemia • The microcirculation develops numerous thrombi

  14. Urinary Tract Infections (UTIs) • UTIs are common 7- to 11-year-old girls • E. coli, the most common pathogen, ascends the urethra in cystitis or the ureter in pyelonephritis • Cystitis • Acute and chronic pyelonephritis

  15. Vesicoureteral Reflux (VUR) • Retrograde flow of urine from the bladder into the ureters • Reflux encourages infected urine from the bladder to be swept up into the kidneys • Leads to frequent pyelonephritis

  16. Vesicoureteral Reflux (VUR) • Caused by a congenital abnormality or ectopic insertion of the ureter into the bladder • Diagnosed by a voiding cystourethrogram (VCUG) and an intravenous pyelogram (IVP)

  17. Vesicoureteral Reflux (VUR)

  18. Wilms Tumor • Wilms tumor is an embryonal tumor of the kidney • Wilms tumor arises from the proliferation of abnormal renal stem cells • Inherited and sporadic forms • Usually found by parent due to abdominal swelling

  19. Enuresis • Involuntary passage of urine by a child who is beyond the age (4 to 5 years old) when voluntary bladder control should have been acquired • Primary enuresis • The child has never been continent • Secondary enuresis • Diurnal, nocturnal, or both

  20. Enuresis • Theories • Organic causes • Maturational lag • Genetic factors • Sleep patterns • Psychosocial theories

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