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Prune belly syndrome
• Triad of bilateral cryptorchidism, deficiency of the abdominal wall musculature, and a dilated, dysmorphic
urinary tract.
• William Osler is credited with giving the syndrome its name “prune belly” in 1901
• Eagle-Barrett syndrome, urethral obstruction malformation complex, the triad syndrome, abdominal muscle
deficiency syndrome, and mesenchymal dysplasia syndrome.
• Prune belly morphology is not confined to the male gender. Females constitute about 3%–5% (pseudo
prune).
• 1/29,000 to 1/40,000 live births.
• The majority are sporadic.
Classification
Theories
•Fetal Outlet Obstruction.
•Theory of Mesodermal Arrest.
•The Yolk Sac Theory.
Fetal outlet
obstruction
Theory of
Mesoderma
l Arrest
Clinical features
Extra genitourinary
manifestations
Abdominal wall
• Wrinkled, floppy abdominal wall, deficiency of underlying muscles, difficult
sitting, difficult walking, chronic constipation, respiratory problems.
• Ventral and lateral muscles: transversus abdominis, rectus abdominis
below the umbilicus, internal oblique, external oblique and rectus
abdominis above the umbilicus.
Genitourinary symptoms
kidney
• Renal dysplasia, hydronephrosis.
• Renal dysplasia of the prune belly syndrome is due to a
combination of a ureteric bud and metanephric defect.
• The renal parenchyma is often well preserved despite a grossly
abnormal drainage system.
• Urinary infection rather than obstruction represents the greatest
threat to the renal parenchyma.
Ureters
• Elongated, tortuous, and dilated.
• The lower one third of the ureter is more profoundly affected than
the proximal portion.
• VUR: up to 85% of patients
• The upper ureter is potentially best suited for definitive
reconstruction, so no ureterostomy to be done.
Bladder
• Thick walled and grossly enlarged, absent trabeculations.
• A patent urachus with urethral atresia or microurethra.
• Splayed trigone.
• Laterally separated UO.
• Wide BN.
• Efficient low-pressure storage and good compliance.
Posterior urethra
• Posterior urethra is dilated, elongated, and tapered at the membranous urethra.
• Utricular diverticulum.
• Vas deferential reflux and small or absent verumontanum.
• True obstructive lesions at the junction of the prostate and membranous urethra
have been described in 20% of infants.
• Stenosis, true valves, atresia, diaphragms, and diverticula.
• Prostatic hypoplasia is one of the etiologies of infertility in this syndrome.
Anterior urethra
• Urethral atresia, megalourethra, Surviving patients with urethral
atresia or microurethra have a patent urachus.
• Scaphoid and fusiform megalourethra.
• Fusiform type is the worst.
Testis
• Bilateral cryptorchidism
• intra-abdominal, overlying the ectatic ureters at the pelvic inlet.
• Risk of malignancy: 30–50 times.
• The gubernaculum is normally attached proximally to the tail of the epididymis,
travels via the inguinal canal, and attaches distally at the pubic tubercle.
• Vas deferens obstruction and epididymal abnormalities associated with maldescent
affect sperm delivery and maturation.
Management
Prenatal evaluation
• As early as 11 weeks of gestation on ultrasound.
• Difficult to distinguish from other causes of obstructive uropathy like
PUV.
• In utero intervention ????
Neonatal evaluation
• Abdominal wall appearance is diagnostic.
• Cardiac and pulmonary evaluation is a must.
• X - ray to rule out pneumothorax and pneumomediastinum.
• 48-72 hours serum creatinine, if >1 in term infant or >1.5 in preterm
>>>> indicate renal insufficiency.
• Starting chemoprophylaxis.
Investigations
• Serum electrolytes.
• serum creatinine.
• Urine analysis and culture.
• Renal and bladder sonogram.
• VCUG.
• MAG 3 renogram vs DMSA.
• MRU.
Initial management
• Watchful waiting to immediate surgical reconstruction of the urinary tract.
• Early surgical intervention in the neonate is avoided, unless a rising creatinine or infection
occurs, requiring early vesicostomy.
• Category I: oligohydramnios, pulmonary hypoplasia, usually die , if passes need for high
urinary diversion like ureterostomy, pyelostomy.
• Category II: if urinary tract infection, vesicostomy, urinary tract reconstruction, orchiopexy,
abdominoplasty is preferred before the age of 1 year.
• Category III: chemoprophylaxis, usually no need for urinary reconstruction, urodynamics,
early orchiopexy and abdominoplasty improves the voiding and defection mechanism.
In utero intervention
• Vesicoamniotic shunting in patients with suspected bladder outlet
obstruction does not improve renal outcomes but would assist in
pulmonary maturation and function.
Anesthetic consideration
• Careful preoperative pulmonary assessment.
• An antecedent history of recurrent respiratory infections warrants
aggressive physiotherapy, postural drainage, and intermittent positive
pressure breathing treatments.
• Specific antibiotic therapy.
• Postoperative analgesics.
Vesicourethral dysfunction
• Internal urethrotomy: trans urethral incision
• Assessment of lower urinary tract dynamics, routine urinary flow
rates, and the amount of residual urine.
• If urinary tract infection or deteriorating renal function in the
perinatal period, a cutaneous vesicostomy is the drainage procedure
of choice.
Reduction cystoplasty
• Bladder volume: 3 L.
• Removal of a dilated urachal diverticulum.
• Some authors do not recommend reduction cystoplasty in light of the
effective and safe application of clean intermittent catheterization
except for the removal of a urachal pseudodiverticulum.
Anterior urethra
• Micro urethra: need for regular dilatation and hydrodistension.
• Megalourethra: hypospadias repair.
Upper urinary tract
• VUR 85%.
• Vesicoureteral obstruction.
• Ureteral valve.
• Decreasing renal function, urinary tract infection.
• Reduction and reimplantation.
Orchiopexy
• Open or laparoscopic.
• Early before the age of 1 year.
• Microvascular testicular auto transplantation, The spermatic vessels
are anastomosed to the inferior epigastric vessels, with microsurgical
vascular techniques.
Abdominal wall reconstruction
• Improve voiding, defecation and sensation of bladder fullness.
• Preservation of the lateral and upper parts of the abdominal wall, the sites of most normal
musculature.
• Ehrlich and Monfort techniques: Abdominal wall reconstruction, utilizing an ellipsoid midline
incision with extensive subcutaneous dissection, and a pants over vest closure.
• This technique preserves the umbilicus, uses the full thickness of abdominal wall, and
provides narrowing at the waist.
• Randolph technique.
Comprehensive reconstruction
• Reduction cystoplasty, resection of the distal ureter and bilateral
ureteral tapered reimplantation.
• Combined with the performance of the abdominoplasty and bilateral
orchiopexy, before the age of 2 years.
• Antibiotic prophylaxis.
Renal transplantation
• Bilateral nephroureterectomies.
• Urodynamic assessment of the lower urinary tract is recommended to
insure absence of obstruction and balanced voiding.
• The use of CIC to empty the decompensated bladder is not a
contraindication to renal transplantation.
• Antibiotic prophylaxis.
• Allograft torsion is an unusual complication, graft loss, was a result of
lack of abdominal wall tone, Nephropexy is recommended.
oshiba prune belly syndrome.pptx

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oshiba prune belly syndrome.pptx

  • 2. • Triad of bilateral cryptorchidism, deficiency of the abdominal wall musculature, and a dilated, dysmorphic urinary tract. • William Osler is credited with giving the syndrome its name “prune belly” in 1901 • Eagle-Barrett syndrome, urethral obstruction malformation complex, the triad syndrome, abdominal muscle deficiency syndrome, and mesenchymal dysplasia syndrome. • Prune belly morphology is not confined to the male gender. Females constitute about 3%–5% (pseudo prune). • 1/29,000 to 1/40,000 live births. • The majority are sporadic.
  • 3.
  • 5.
  • 6. Theories •Fetal Outlet Obstruction. •Theory of Mesodermal Arrest. •The Yolk Sac Theory.
  • 11. Abdominal wall • Wrinkled, floppy abdominal wall, deficiency of underlying muscles, difficult sitting, difficult walking, chronic constipation, respiratory problems. • Ventral and lateral muscles: transversus abdominis, rectus abdominis below the umbilicus, internal oblique, external oblique and rectus abdominis above the umbilicus.
  • 12.
  • 13.
  • 15. kidney • Renal dysplasia, hydronephrosis. • Renal dysplasia of the prune belly syndrome is due to a combination of a ureteric bud and metanephric defect. • The renal parenchyma is often well preserved despite a grossly abnormal drainage system. • Urinary infection rather than obstruction represents the greatest threat to the renal parenchyma.
  • 16. Ureters • Elongated, tortuous, and dilated. • The lower one third of the ureter is more profoundly affected than the proximal portion. • VUR: up to 85% of patients • The upper ureter is potentially best suited for definitive reconstruction, so no ureterostomy to be done.
  • 17.
  • 18.
  • 19. Bladder • Thick walled and grossly enlarged, absent trabeculations. • A patent urachus with urethral atresia or microurethra. • Splayed trigone. • Laterally separated UO. • Wide BN. • Efficient low-pressure storage and good compliance.
  • 20.
  • 21. Posterior urethra • Posterior urethra is dilated, elongated, and tapered at the membranous urethra. • Utricular diverticulum. • Vas deferential reflux and small or absent verumontanum. • True obstructive lesions at the junction of the prostate and membranous urethra have been described in 20% of infants. • Stenosis, true valves, atresia, diaphragms, and diverticula. • Prostatic hypoplasia is one of the etiologies of infertility in this syndrome.
  • 22. Anterior urethra • Urethral atresia, megalourethra, Surviving patients with urethral atresia or microurethra have a patent urachus. • Scaphoid and fusiform megalourethra. • Fusiform type is the worst.
  • 23.
  • 24. Testis • Bilateral cryptorchidism • intra-abdominal, overlying the ectatic ureters at the pelvic inlet. • Risk of malignancy: 30–50 times. • The gubernaculum is normally attached proximally to the tail of the epididymis, travels via the inguinal canal, and attaches distally at the pubic tubercle. • Vas deferens obstruction and epididymal abnormalities associated with maldescent affect sperm delivery and maturation.
  • 26. Prenatal evaluation • As early as 11 weeks of gestation on ultrasound. • Difficult to distinguish from other causes of obstructive uropathy like PUV. • In utero intervention ????
  • 27. Neonatal evaluation • Abdominal wall appearance is diagnostic. • Cardiac and pulmonary evaluation is a must. • X - ray to rule out pneumothorax and pneumomediastinum. • 48-72 hours serum creatinine, if >1 in term infant or >1.5 in preterm >>>> indicate renal insufficiency. • Starting chemoprophylaxis.
  • 28. Investigations • Serum electrolytes. • serum creatinine. • Urine analysis and culture. • Renal and bladder sonogram. • VCUG. • MAG 3 renogram vs DMSA. • MRU.
  • 29. Initial management • Watchful waiting to immediate surgical reconstruction of the urinary tract. • Early surgical intervention in the neonate is avoided, unless a rising creatinine or infection occurs, requiring early vesicostomy. • Category I: oligohydramnios, pulmonary hypoplasia, usually die , if passes need for high urinary diversion like ureterostomy, pyelostomy. • Category II: if urinary tract infection, vesicostomy, urinary tract reconstruction, orchiopexy, abdominoplasty is preferred before the age of 1 year. • Category III: chemoprophylaxis, usually no need for urinary reconstruction, urodynamics, early orchiopexy and abdominoplasty improves the voiding and defection mechanism.
  • 30. In utero intervention • Vesicoamniotic shunting in patients with suspected bladder outlet obstruction does not improve renal outcomes but would assist in pulmonary maturation and function.
  • 31. Anesthetic consideration • Careful preoperative pulmonary assessment. • An antecedent history of recurrent respiratory infections warrants aggressive physiotherapy, postural drainage, and intermittent positive pressure breathing treatments. • Specific antibiotic therapy. • Postoperative analgesics.
  • 32. Vesicourethral dysfunction • Internal urethrotomy: trans urethral incision • Assessment of lower urinary tract dynamics, routine urinary flow rates, and the amount of residual urine. • If urinary tract infection or deteriorating renal function in the perinatal period, a cutaneous vesicostomy is the drainage procedure of choice.
  • 33. Reduction cystoplasty • Bladder volume: 3 L. • Removal of a dilated urachal diverticulum. • Some authors do not recommend reduction cystoplasty in light of the effective and safe application of clean intermittent catheterization except for the removal of a urachal pseudodiverticulum.
  • 34.
  • 35.
  • 36. Anterior urethra • Micro urethra: need for regular dilatation and hydrodistension. • Megalourethra: hypospadias repair.
  • 37. Upper urinary tract • VUR 85%. • Vesicoureteral obstruction. • Ureteral valve. • Decreasing renal function, urinary tract infection. • Reduction and reimplantation.
  • 38. Orchiopexy • Open or laparoscopic. • Early before the age of 1 year. • Microvascular testicular auto transplantation, The spermatic vessels are anastomosed to the inferior epigastric vessels, with microsurgical vascular techniques.
  • 39. Abdominal wall reconstruction • Improve voiding, defecation and sensation of bladder fullness. • Preservation of the lateral and upper parts of the abdominal wall, the sites of most normal musculature. • Ehrlich and Monfort techniques: Abdominal wall reconstruction, utilizing an ellipsoid midline incision with extensive subcutaneous dissection, and a pants over vest closure. • This technique preserves the umbilicus, uses the full thickness of abdominal wall, and provides narrowing at the waist. • Randolph technique.
  • 40.
  • 41.
  • 42.
  • 43.
  • 44.
  • 45. Comprehensive reconstruction • Reduction cystoplasty, resection of the distal ureter and bilateral ureteral tapered reimplantation. • Combined with the performance of the abdominoplasty and bilateral orchiopexy, before the age of 2 years. • Antibiotic prophylaxis.
  • 46.
  • 47.
  • 48.
  • 49. Renal transplantation • Bilateral nephroureterectomies. • Urodynamic assessment of the lower urinary tract is recommended to insure absence of obstruction and balanced voiding. • The use of CIC to empty the decompensated bladder is not a contraindication to renal transplantation. • Antibiotic prophylaxis. • Allograft torsion is an unusual complication, graft loss, was a result of lack of abdominal wall tone, Nephropexy is recommended.