MEGAURETER  

 

Megaureter may be seen alone or in association with dilatation of the renal pelvis and calyces.
 

ETIOLOGY

 

CLASSIFICATION

      Primary megaureter or megaloureter is an uncommon cause of severe hydronephrosis (1). It includes all cases of megaureter associated with idiopathic congenital abnormality at the UVJ. The exact etiology of these is unknown.

  

           Belman (2) defined 3 types of primary megaureter:

·         Obstructed:

o       The obstructed variety is really caused by a functional obstruction theoretically of similar etiology to the UPJ obstruction but at the distal end of the ureter (ie, deficiency of ureteral smooth muscle fibers leading to limited peristalsis).

o       It usually involves the distal 2 cm (0.5–4 cm) of ureter.

o       The abnormal ureter is of normal calibre.

o       More proximal ureter, usually the distal third, but at times the entire ureter and even the pelvis are dilated.

o       The ureteral orifice and the submucosal tunnel are normal

·         Refluxing -  may be caused by a short or absent intravesicle ureter or a paraureteric diverticulum.

·         Nonrefluxing unobstructed. - The nonobstructing nonrefluxing megaureter is caused neither by reflux or stenosis and is the most common type of magaureter in neonates. Further imaging information is necessary to exclude secondary causes of megaureter such as posterior urethral valves, urethral stricture, ureterocele, or neurogenic bladder. Voiding cystourethrography (VCU) will exclude reflux.

 

 

 

ULTRASOUND



 

 

 

ASSOCIATIONS

 

REFERENCES

 

  1. V. Gylys-Morin, E. Minevich, L. Tackett et al., Magnetic resonance imaging of the dysplastic renal moiety and ectopic ureter. J Urol 164 (2000), pp. 2034–2039.
  2. B.A. Belman, A perspective on vesicoureteral reflux. Urol Clin North Am 22 (1995), pp. 139–150.