Aim. Ureteropelvic junction obstruction (UPJO) is rarely associated with a duplex collecting system. We review this unusual anomaly in terms of presentation, diagnostic evaluation, and surgical management. Method. We retrospectively reviewed the medical records of patients diagnosed with a duplex system with UPJO. Result. Sixteen patients (6 girls, 10 boys) with 18 moieties were treated surgically and four patients were treated conservatively. The median age at surgery was two years (range, 2 months to 7 years). The lower pole and upper moiety were affected in 12 and two kidneys, respectively, and both were affected in two patients. The anomaly was right-sided in 12 moieties and left-sided in six. The duplication was incomplete in seven pat...
Background: Ureteropelvic junction obstruction (UPJO) is often encountered in patients with a horses...
Retroiliac ureter is a rare congenital anomaly. In this paper, we present a case in which retroiliac...
Retroiliac ureter is a rare congenital anomaly. In this paper, we present a case in which retroiliac...
Aim. Ureteropelvic junction obstruction (UPJO) is rarely associated with a duplex collecting system....
Ureteropelvic junction obstruction and duplicated collecting system are common urologic anomalies in...
Two examples of the rare case of complete duplicated collecting system with lower pole ureteropelvic...
We present a case of UPJO associated with an incompletely duplicated collecting system in a horsesho...
Abstract Introduction There are only a few reports on laparoscopic pyeloplasty in kidney abnormaliti...
To investigate the diagnosis, treatment and surgical outcomes of ureteropelvic junction obstruction ...
Duplex collecting system is presence of two pelvicalyceal system which is associated with single or ...
Purpose We report our experience in the management of ureteropelvic junction obstruction in childre...
AbstractWe present a case of UPJO associated with an incompletely duplicated collecting system in a ...
Duplication of the ureters is a common anomaly and is frequently encountered by radiologists. Duplic...
The presence of an ectopic ureter may be indicated by continuous wetting, seen especially in girls. ...
Congenital anomalies of the kidney and urinary tract are part of a family of diseases with different...
Background: Ureteropelvic junction obstruction (UPJO) is often encountered in patients with a horses...
Retroiliac ureter is a rare congenital anomaly. In this paper, we present a case in which retroiliac...
Retroiliac ureter is a rare congenital anomaly. In this paper, we present a case in which retroiliac...
Aim. Ureteropelvic junction obstruction (UPJO) is rarely associated with a duplex collecting system....
Ureteropelvic junction obstruction and duplicated collecting system are common urologic anomalies in...
Two examples of the rare case of complete duplicated collecting system with lower pole ureteropelvic...
We present a case of UPJO associated with an incompletely duplicated collecting system in a horsesho...
Abstract Introduction There are only a few reports on laparoscopic pyeloplasty in kidney abnormaliti...
To investigate the diagnosis, treatment and surgical outcomes of ureteropelvic junction obstruction ...
Duplex collecting system is presence of two pelvicalyceal system which is associated with single or ...
Purpose We report our experience in the management of ureteropelvic junction obstruction in childre...
AbstractWe present a case of UPJO associated with an incompletely duplicated collecting system in a ...
Duplication of the ureters is a common anomaly and is frequently encountered by radiologists. Duplic...
The presence of an ectopic ureter may be indicated by continuous wetting, seen especially in girls. ...
Congenital anomalies of the kidney and urinary tract are part of a family of diseases with different...
Background: Ureteropelvic junction obstruction (UPJO) is often encountered in patients with a horses...
Retroiliac ureter is a rare congenital anomaly. In this paper, we present a case in which retroiliac...
Retroiliac ureter is a rare congenital anomaly. In this paper, we present a case in which retroiliac...