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Megaureter ppt. Types, pathophysiology, evaluation and management.
 Normal ureteral diameter in children is rarely > 5 
mm 
 Ureters > 7 mm are considered MGUs 
 The dilated ureter or MGU can be classified into 
one of four groups based on the cause of the 
dilatation: 
› (1) refluxing 
› (2) obstructed 
› (3) both refluxing and obstructed 
› (4) both nonrefluxing and nonobstructed.
 In one series, MGU comprised 20% of 
antenatally diagnosed urologic anomalies, 
much higher than in historical series b/c most 
were discovered only after they became 
symptomatic 
 If left undetected, many MGUs might never 
become symptomatic 
› An observation that raises serious questions with 
regard to treatment
Megaureter ppt. Types, pathophysiology, evaluation and management.
 Common finding in neonates referred for 
urologic evaluation. 
 Prenatal USG series suggest UVJ 
obstruction in up to 23% of patients with 
urinary tract dilatation. 
 Primary MGU is two to four times more 
common in boys than girls, has a slight 
prediction (1.6 to 4.5 times) for left side 
and is bilateral in app 25% of patients.
 In up to10% to 15% of children the contra 
lateral kidney may be absent or 
dysplastic and concomitant obstruction 
of the ipsilateral UPJ area has been 
described on rare occasion. 
 No clear evidence of hereditary 
predisposition. 
 Clinically patients have UTIs, PAIN or 
HEMATURIA.
 The distal end of ureter as it becomes 
intramural and subsequently sub mucosal, 
rearranges the muscular layers in its wall. 
 All layers become longitudinally oriented 
and the ureteral adventitia fuses to the 
bladder trigone by attachment to 
Waldyer’s sheath. 
 Sympathetic and parasympathetic 
innervations to the distal ureter and UVJ 
area is believed to modulate primarily 
ureteral peristalsis; however its exact role in 
regulating urine transport is unclear
 Primary refluxing megaureters are associated 
with congenital anomalies of the UVJ where a 
deficiency of the longitudinal muscle of the 
intravesical ureter results in an inadequate 
valvular mechanism 
 Secondary refulxing megaureters are caused by 
bladder obstruction and the elevated 
pressures that accompany it 
› Examples include PUV (most common) as well as 
neurogenic bladders and non-neurogenic 
neurogenic bladders and Prune Belly Syndrome.
ALOO BUKHARA
Megaureter ppt. Types, pathophysiology, evaluation and management.
 secondary to PUV or NGB when elevated bladder pressures 
cause decompensation of the UVJ.
 The cause of primary obstructive MGU typically is 
an aperistaltic juxtavesical segment 3 to 4 cm 
long that is unable to propagate urine at 
acceptable rates of flow 
 True stenosis is rare, but histologic disorientation 
of muscle, muscular hypoplasia, muscular 
hypertrophy, mural fibrosis and excess collagen 
deposition (Type 1) have been described
 Altered peristalsis prevents the free outflow of 
urine 
› Retrograde regurgitation occurs as urine boluses are 
unable to fully traverse the aberrant distal segment 
 Resulting ureteral dilatation depends on the 
amount of urine that is forced to coalesce 
proximally because of incomplete passage. 
 Other rare causes of primary obstructive MGU 
include congenital ureteral strictures and 
ureteral valves
Megaureter ppt. Types, pathophysiology, evaluation and management.
 Most commonly occurs with neurogenic and non-neurogenic 
voiding dysfunction or infravesical 
obstructions such as PUV 
 The ureter struggles with propulsion of urine 
when pressure is > 40 cm H2O across the UVJ. 
 Ureteral dilatation, decompensation of the UVJ, 
reflux, and renal damage result if pressures 
continue unchecked 
 Dilatation largely resolves once the elevated 
intravesical pressures are addressed
 Sometimes, the ureter remains dilated due to altered 
compliance or a damaged peristaltic mechanisms. 
› Transmural scarring from chronic infection is seen in some cases. 
› Obstruction is not truly present but elevated intravesical pressures 
are projected proximally as a noncompliant column 
 Other obstructive causes of ureteral dilatation include 
ureteroceles, ureteral ectopia, bladder diverticula, 
periureteral postreimplantation fibrosis, neurogenic 
bladder, and external compression by retroperitoneal 
tumors, masses, or aberrant vessels
 Once VUR, obstruction, and secondary causes of 
dilatation have been ruled out diagnosis of primary 
nonrefluxing, nonobstructive MGU 
› Most newborn MGUs fall in this category 
 Possible causes: increased fetal UOP, persistent 
fetal folds, delayed ureteral patency, immature 
peristalsis, hyperreflexic bladder of infancy, 
transient urethral obstruction
 The newborn ureter is a more compliant 
conduit than that of the adult 
 The kidneys of newborns are probably better 
buffered from the pressures of any partial or 
transient obstructions that might occur early 
in development than are kidneys obstructed 
at more proximal levels (UPJ) or at a later 
age
 More common than originally thought, and often 
have an identifiable cause 
 Can result from acute UTI with bacterial 
endotoxins that inhibit peristalsis 
› Resolution with appropriate antibiotic therapy 
 Nephropathies and other conditions lead to 
increased UOP that overwhelm max peristalsis 
which leads to progressive dilatation
 These include lithium toxicity, diabetes 
insipidus or mellitus, sickle cell nephropathy, 
and psychogenic polydipsia 
 The most extreme examples of nonobstructed 
ureteral dilatations occur with the prune-belly 
syndrome
 Studies showed that clinically significant MGU 
accounted for 8% of children found to have 
hydronephrosis on imaging studies, preceded 
by UPJ obstruction 22%, PUV 19% andectopic 
ureterocele 14%. 
 MGU are reported to occur in app 23% of 
neonates noted to have antenatal 
hydroureteronephrosis. 
 Ranking 2nd in D/D of neonates with 
hydronephrosis after UPJ obstruction. 
 More often in boys and on left side.
 Ultrasound is the initial study obtained in any 
child with a suspected urinary abnormality 
 Usually distinguishes MGU from UPJ as the 
most common cause of hydronephrosis 
 Provides useful anatomic detail of the renal 
parenchyma, collecting system, and bladder 
 Baseline standard for the degree of 
hydroureteronephrosis for serial future studies
Megaureter ppt. Types, pathophysiology, evaluation and management.
 The presence of ureteral dilatation 
› VCUG to rule out reflux and assess the quality of 
the bladder and urethra 
 Neurogenic dysfunction or outlet obstruction 
are common causes of secondary MGU 
 Need to assess renal function
 Renal scans offers objective, reproducible parameters of 
function and obstruction 
 99m Tc-DTPA and 99m Tc-Mertiatide (MAG3) are most 
commonly used assess function and clearance. 
 Renal scan shortcomings: standardized tracer dosing, 
timing in diuretic dosing, and patient hydration ensure 
valid comparison of results 
 should defer the study for 3 months for glomerular 
maturation 
 Scans that evaluate drainage (half-life) alone routinely 
yield values indicative of obstruction because of the 
dilatation of the collecting system
 Renal scan estimate GFR and absolute renal 
function by measuring the uptake of radionuclide 
(DTPA) early after its systemic administration 
 This may indicate the impact of megaureter on 
renal parenchymal level, rather than within the 
collecting system, where slow rates of washout 
are to be expected because of dilatation 
 Magnetic resonance urography has the 
capability of providing greater anatomic 
abnormalities. 
 Percutaneous perfusion studies (Whitaker 
perfusion test) can also be used.
Megaureter ppt. Types, pathophysiology, evaluation and management.
 Routinely recommending surgery in newborns and 
infants with grades IV-V reflux is not appropriate 
 Medical management is appropriate during infancy and is 
continued if a trend to resolution is noted 
 Surgery remains the recommendation for persistent high-grade 
reflux in older children and adults 
 In the rare infant for whom medical management has 
failed but who is considered too small for reconstructive 
surgery, distal ureterostomy for unilateral reflux or 
vesicostomy for bilateral disease provides an ideal 
temporizing solution
 Management of secondary MGUs is directed at their cause 
 Reflux and dilatation improve with the ablation of PUV or 
medical management of neurogenic bladder 
 MGUs from prune-belly syndrome, diabetes insipidus, or 
infection, require no more than observation alone 
 Some degree of nonobstructed hydroureteronephrosis 
usually persists, even after primary or secondary causes 
have been corrected 
 Re-evaluation is often necessary
 The complication rate of surgery is higher in infants 
› repeat surgeries were required for 12% infants 
operated on before 8 mo in one series 
 As long as renal function is stable and UTIs are not 
a problem, expectant management is preferred 
 Antibiotic suppression with close radiologic 
surveillance is appropriate in most cases 
 U/A and RUS every 3 to 6 months during the first 
year
 Severe hydroureteronephrosis that shows no 
signs of improvement or the clinical status 
worsens, correction is undertaken when it is 
technically feasible, usually between the ages of 1 
and 2 years. 
 For the occasional newborn who presents with 
massive ureteral dilatation or poor renal function 
(which is rare with MGUs) or develops recurrent 
infections, distal ureterostomy provides an 
effective means for poor drainage until the child is 
old enough to undergo reimplantation.
 Ureteral tailoring is usually necessary to achieve 
the proper length-to-diameter ratio 
 Narrowing of the ureter may enable the walls to 
coapt, leading to more effective peristalsis 
 Revising the distal segment intended for 
reimplantation is all that is usually required 
 The proximal segments regain tone once they 
are unobstructed. Kinking is usually 
nonobstructive and will resolve. 
 Extended stent drainage after tapering 
decompresses the system 
› Leads to peristaltic recovery
 Plication or infolding is useful for the moderately 
dilated ureter. 
 Ureteral vascularity is preserved, and the revision 
can be taken down and redone if vascular 
compromise is suspected 
 Bulk is a problem with the extremely large ureter 
 Excisional tapering is preferred for the more 
severely dilatated or thickened ureter 
› Plication of ureters greater than 1.75 cm in diameter 
experienced more complications in one series
 Remodeled MGUs have been generally 
reimplanted with standard cross-trigonal or 
Leadbetter-type techniques 
 Extravesical repairs can also be successfully 
done 
 The success with reimplantation of remodeled 
MGUs is 90-95% regardless of technique 
› Compares to 95-99% of non-megaureter reimplants
 Tapering 
 Starr Plication 
 Kalicinski Plication
Megaureter ppt. Types, pathophysiology, evaluation and management.
Megaureter ppt. Types, pathophysiology, evaluation and management.
Megaureter ppt. Types, pathophysiology, evaluation and management.
 Politano-Leadbetter Technique 
 Cohen Cross-Trigonal Technique 
 Glenn-Anderson Technique 
 Gil-Vernet Technique
Megaureter ppt. Types, pathophysiology, evaluation and management.
Megaureter ppt. Types, pathophysiology, evaluation and management.
 The reimplantation of MGUs has the same 
complications (i.e., persistent reflux and 
obstruction) as that of nondilated ureters, but at 
increased rates 
 Complications can occur regardless of whether 
excisional tapering or a folding technique is used 
 Better results with obstructive MGU and higher 
rates of unresolved reflux after tailoring of 
refluxing variants 
› Higher incidence of bladder dysfunction associated 
with the latter and more dramatic abnormalities of their 
musculature.
 Increased collagen deposition in refluxing MGUs 
and altered smooth muscle ratios 
 In contrast, obstructive MGUs were not found to 
be statistically different from controls 
 Increased levels of type III collagen in refluxing 
MGUs 
› Leads to an intrinsically stiffer ureter that lessens the 
surgical success in reimplantation 
 Rarely, reflux persists despite adequate ureteral 
tunnels in both tapered and normal-sized 
ureters. 
› Leads to intrinsic ureteral dysfunction caused by 
transmural scarring
Megaureter ppt. Types, pathophysiology, evaluation and management.

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Megaureter ppt. Types, pathophysiology, evaluation and management.

  • 2.  Normal ureteral diameter in children is rarely > 5 mm  Ureters > 7 mm are considered MGUs  The dilated ureter or MGU can be classified into one of four groups based on the cause of the dilatation: › (1) refluxing › (2) obstructed › (3) both refluxing and obstructed › (4) both nonrefluxing and nonobstructed.
  • 3.  In one series, MGU comprised 20% of antenatally diagnosed urologic anomalies, much higher than in historical series b/c most were discovered only after they became symptomatic  If left undetected, many MGUs might never become symptomatic › An observation that raises serious questions with regard to treatment
  • 5.  Common finding in neonates referred for urologic evaluation.  Prenatal USG series suggest UVJ obstruction in up to 23% of patients with urinary tract dilatation.  Primary MGU is two to four times more common in boys than girls, has a slight prediction (1.6 to 4.5 times) for left side and is bilateral in app 25% of patients.
  • 6.  In up to10% to 15% of children the contra lateral kidney may be absent or dysplastic and concomitant obstruction of the ipsilateral UPJ area has been described on rare occasion.  No clear evidence of hereditary predisposition.  Clinically patients have UTIs, PAIN or HEMATURIA.
  • 7.  The distal end of ureter as it becomes intramural and subsequently sub mucosal, rearranges the muscular layers in its wall.  All layers become longitudinally oriented and the ureteral adventitia fuses to the bladder trigone by attachment to Waldyer’s sheath.  Sympathetic and parasympathetic innervations to the distal ureter and UVJ area is believed to modulate primarily ureteral peristalsis; however its exact role in regulating urine transport is unclear
  • 8.  Primary refluxing megaureters are associated with congenital anomalies of the UVJ where a deficiency of the longitudinal muscle of the intravesical ureter results in an inadequate valvular mechanism  Secondary refulxing megaureters are caused by bladder obstruction and the elevated pressures that accompany it › Examples include PUV (most common) as well as neurogenic bladders and non-neurogenic neurogenic bladders and Prune Belly Syndrome.
  • 11.  secondary to PUV or NGB when elevated bladder pressures cause decompensation of the UVJ.
  • 12.  The cause of primary obstructive MGU typically is an aperistaltic juxtavesical segment 3 to 4 cm long that is unable to propagate urine at acceptable rates of flow  True stenosis is rare, but histologic disorientation of muscle, muscular hypoplasia, muscular hypertrophy, mural fibrosis and excess collagen deposition (Type 1) have been described
  • 13.  Altered peristalsis prevents the free outflow of urine › Retrograde regurgitation occurs as urine boluses are unable to fully traverse the aberrant distal segment  Resulting ureteral dilatation depends on the amount of urine that is forced to coalesce proximally because of incomplete passage.  Other rare causes of primary obstructive MGU include congenital ureteral strictures and ureteral valves
  • 15.  Most commonly occurs with neurogenic and non-neurogenic voiding dysfunction or infravesical obstructions such as PUV  The ureter struggles with propulsion of urine when pressure is > 40 cm H2O across the UVJ.  Ureteral dilatation, decompensation of the UVJ, reflux, and renal damage result if pressures continue unchecked  Dilatation largely resolves once the elevated intravesical pressures are addressed
  • 16.  Sometimes, the ureter remains dilated due to altered compliance or a damaged peristaltic mechanisms. › Transmural scarring from chronic infection is seen in some cases. › Obstruction is not truly present but elevated intravesical pressures are projected proximally as a noncompliant column  Other obstructive causes of ureteral dilatation include ureteroceles, ureteral ectopia, bladder diverticula, periureteral postreimplantation fibrosis, neurogenic bladder, and external compression by retroperitoneal tumors, masses, or aberrant vessels
  • 17.  Once VUR, obstruction, and secondary causes of dilatation have been ruled out diagnosis of primary nonrefluxing, nonobstructive MGU › Most newborn MGUs fall in this category  Possible causes: increased fetal UOP, persistent fetal folds, delayed ureteral patency, immature peristalsis, hyperreflexic bladder of infancy, transient urethral obstruction
  • 18.  The newborn ureter is a more compliant conduit than that of the adult  The kidneys of newborns are probably better buffered from the pressures of any partial or transient obstructions that might occur early in development than are kidneys obstructed at more proximal levels (UPJ) or at a later age
  • 19.  More common than originally thought, and often have an identifiable cause  Can result from acute UTI with bacterial endotoxins that inhibit peristalsis › Resolution with appropriate antibiotic therapy  Nephropathies and other conditions lead to increased UOP that overwhelm max peristalsis which leads to progressive dilatation
  • 20.  These include lithium toxicity, diabetes insipidus or mellitus, sickle cell nephropathy, and psychogenic polydipsia  The most extreme examples of nonobstructed ureteral dilatations occur with the prune-belly syndrome
  • 21.  Studies showed that clinically significant MGU accounted for 8% of children found to have hydronephrosis on imaging studies, preceded by UPJ obstruction 22%, PUV 19% andectopic ureterocele 14%.  MGU are reported to occur in app 23% of neonates noted to have antenatal hydroureteronephrosis.  Ranking 2nd in D/D of neonates with hydronephrosis after UPJ obstruction.  More often in boys and on left side.
  • 22.  Ultrasound is the initial study obtained in any child with a suspected urinary abnormality  Usually distinguishes MGU from UPJ as the most common cause of hydronephrosis  Provides useful anatomic detail of the renal parenchyma, collecting system, and bladder  Baseline standard for the degree of hydroureteronephrosis for serial future studies
  • 24.  The presence of ureteral dilatation › VCUG to rule out reflux and assess the quality of the bladder and urethra  Neurogenic dysfunction or outlet obstruction are common causes of secondary MGU  Need to assess renal function
  • 25.  Renal scans offers objective, reproducible parameters of function and obstruction  99m Tc-DTPA and 99m Tc-Mertiatide (MAG3) are most commonly used assess function and clearance.  Renal scan shortcomings: standardized tracer dosing, timing in diuretic dosing, and patient hydration ensure valid comparison of results  should defer the study for 3 months for glomerular maturation  Scans that evaluate drainage (half-life) alone routinely yield values indicative of obstruction because of the dilatation of the collecting system
  • 26.  Renal scan estimate GFR and absolute renal function by measuring the uptake of radionuclide (DTPA) early after its systemic administration  This may indicate the impact of megaureter on renal parenchymal level, rather than within the collecting system, where slow rates of washout are to be expected because of dilatation  Magnetic resonance urography has the capability of providing greater anatomic abnormalities.  Percutaneous perfusion studies (Whitaker perfusion test) can also be used.
  • 28.  Routinely recommending surgery in newborns and infants with grades IV-V reflux is not appropriate  Medical management is appropriate during infancy and is continued if a trend to resolution is noted  Surgery remains the recommendation for persistent high-grade reflux in older children and adults  In the rare infant for whom medical management has failed but who is considered too small for reconstructive surgery, distal ureterostomy for unilateral reflux or vesicostomy for bilateral disease provides an ideal temporizing solution
  • 29.  Management of secondary MGUs is directed at their cause  Reflux and dilatation improve with the ablation of PUV or medical management of neurogenic bladder  MGUs from prune-belly syndrome, diabetes insipidus, or infection, require no more than observation alone  Some degree of nonobstructed hydroureteronephrosis usually persists, even after primary or secondary causes have been corrected  Re-evaluation is often necessary
  • 30.  The complication rate of surgery is higher in infants › repeat surgeries were required for 12% infants operated on before 8 mo in one series  As long as renal function is stable and UTIs are not a problem, expectant management is preferred  Antibiotic suppression with close radiologic surveillance is appropriate in most cases  U/A and RUS every 3 to 6 months during the first year
  • 31.  Severe hydroureteronephrosis that shows no signs of improvement or the clinical status worsens, correction is undertaken when it is technically feasible, usually between the ages of 1 and 2 years.  For the occasional newborn who presents with massive ureteral dilatation or poor renal function (which is rare with MGUs) or develops recurrent infections, distal ureterostomy provides an effective means for poor drainage until the child is old enough to undergo reimplantation.
  • 32.  Ureteral tailoring is usually necessary to achieve the proper length-to-diameter ratio  Narrowing of the ureter may enable the walls to coapt, leading to more effective peristalsis  Revising the distal segment intended for reimplantation is all that is usually required  The proximal segments regain tone once they are unobstructed. Kinking is usually nonobstructive and will resolve.  Extended stent drainage after tapering decompresses the system › Leads to peristaltic recovery
  • 33.  Plication or infolding is useful for the moderately dilated ureter.  Ureteral vascularity is preserved, and the revision can be taken down and redone if vascular compromise is suspected  Bulk is a problem with the extremely large ureter  Excisional tapering is preferred for the more severely dilatated or thickened ureter › Plication of ureters greater than 1.75 cm in diameter experienced more complications in one series
  • 34.  Remodeled MGUs have been generally reimplanted with standard cross-trigonal or Leadbetter-type techniques  Extravesical repairs can also be successfully done  The success with reimplantation of remodeled MGUs is 90-95% regardless of technique › Compares to 95-99% of non-megaureter reimplants
  • 35.  Tapering  Starr Plication  Kalicinski Plication
  • 39.  Politano-Leadbetter Technique  Cohen Cross-Trigonal Technique  Glenn-Anderson Technique  Gil-Vernet Technique
  • 42.  The reimplantation of MGUs has the same complications (i.e., persistent reflux and obstruction) as that of nondilated ureters, but at increased rates  Complications can occur regardless of whether excisional tapering or a folding technique is used  Better results with obstructive MGU and higher rates of unresolved reflux after tailoring of refluxing variants › Higher incidence of bladder dysfunction associated with the latter and more dramatic abnormalities of their musculature.
  • 43.  Increased collagen deposition in refluxing MGUs and altered smooth muscle ratios  In contrast, obstructive MGUs were not found to be statistically different from controls  Increased levels of type III collagen in refluxing MGUs › Leads to an intrinsically stiffer ureter that lessens the surgical success in reimplantation  Rarely, reflux persists despite adequate ureteral tunnels in both tapered and normal-sized ureters. › Leads to intrinsic ureteral dysfunction caused by transmural scarring