1.Two Cases of Ureterocele.
Jong Han CHOI ; In Ho SONG ; Woon Hyung LEE
Korean Journal of Urology 1971;12(1):113-116
No abstract available.
Ureterocele*
2.Two Cases of Duplicated Collecting System with Lower Pole Ureteropelvic Juncton Obstruction.
Woo Jin KO ; Chang Hee HONG ; Soo Yeon CHANG ; Sang Won HAN
Journal of the Korean Society of Pediatric Nephrology 2000;4(2):170-174
Ureteropelvic junction obstruction and duplicated collecting system are common urologic anomalies in upper urinary system, but they seldom occur in combination. These obstruction can occur in both partial or complete duplicated collecting system. Complete duplication of the ureter may be asymptomatic or recognized when complications develop as a result of reflux into the lower pole ureter or obstruction of the upper pole with an ectopic ureterocele. It is difficult to choose an optimal therapy due to the high variability in function, degree of obsturction, damage and potential for regeneration in growing kidney. We report our experience of successful surgical interventions in the ureteropelvic junction obstruction of the lower pole with complete duplicated collecting system.
Kidney
;
Regeneration
;
Ureter
;
Ureterocele
3.Surgical correction of two cases of ureterocele that prenatal diagnosed
Journal of Vietnamese Medicine 2001;263(9):222-228
The authors report two infants with unilateral duplex ureteroceles treated successfully by simplified operation at the age of 3 months and 11 months. Both had been prenatally diagnosed by ultrasound at the 24th and 32nd week of gestation. By the way the authors suggest the importance of prenatal diagnosis and monitor the evolution in order to plan an early postnatal surgical correction
Ureterocele
;
Prenatal Diagnosis
4.Clinical and paraclinical features and the treatment of ureterocele
Journal of Medical and Pharmaceutical Information 1998;(1):34-47
Between April 1992 and March 2001, a total of 52 patients (58 ureteroceles) was diagnosed and treated at National Pediatric Institute. For ureterocele, female to male ratio was 5.2:1. Complete duplication was found in association with the ureterocele in 50 cases. Urinary tract infection was the most frequent mode of presentation (64%), abdominal mass (12%) and prolapsed ureterocele (13%). The diagnostic procedure included ultrasonographic examination, voiding cystourethrography and excretory urogram. Of 52 patients, 82% and 77% were less than 2 years old at presentation and operation respectively. The elective surgical policy was individualized, based on renal function and presence of vesicoureteral reflux. Overall results within various groups were generally satisfactory regarding the eradication of urinary tract infection, the preservation of renal function in 73% cases after the first procedures
Ureterocele
;
therapeutics
;
diagnosis
5.Double Kidneys, Double Ureters and Ureterocele in Identical Female Twins.
Ran NAMKUNG ; Do Kwang YUN ; Jun Hee SUL ; Jae Seung LEE ; Pyung Kil KIM ; Jin Moo LEE
Journal of the Korean Pediatric Society 1981;24(2):145-152
No abstract available.
Female*
;
Humans
;
Kidney*
;
Ureter*
;
Ureterocele*
6.Ectopic ureterocele in children.
Jong Gag PARK ; Chun Il KIM ; Kwang Sae KIM
Korean Journal of Urology 1991;32(3):391-398
Ectopic ureteroceles have a broad spectrum of presentation, anatomy and pathophysiology and the management is controversial. Herein, we report our experience of the management in 7 children with 8 ectopic ureteroceles associated with complete duplicated systems. Two functioning upper renal segments were able to be salvaged with ureteropyeIostomy and common sheath ureteral reimplantation. Four small ureteroceles not associated with reflux managed successfully with upper tract correction only(3 heminephrectomy and 1 ureteropyelostomy). Three children with ectopic ureteroceles associated with reflux and/or outlet obstruction underwent successful one stage total reconstruction which included heminephrectomy, ureterectomy, ureterocelectomy and lower pole ureter reimplantation. In summary, the management of ectopic ureterocele must be individualized taking into considerations the salvageability of renal segments, presence of reflux and/or outlet obstruction.
Child*
;
Humans
;
Replantation
;
Ureter
;
Ureterocele*
7.Ultrasonography of Congenital Hydronephrosis.
Journal of the Korean Society of Medical Ultrasound 2013;32(2):103-110
Hydronephrosis is the most common urogenital anomaly with the potential for obstructive process. And ultrasonography, as a first-line imaging modality, is a useful tool for evaluation of prenatal and postnatal hydronephrosis, even though evaluation of renal function is still needed. In this article, we review the common causes of congenital hydronephrosis and the sonographic findings of those diseases.
Hydronephrosis
;
Ureterocele
;
Vesico-Ureteral Reflux
8.Two Cases of Intravesical Ureterocele Including Calculus.
Tong Choon PARK ; Sae Chul KIM ; Sae Kook CHANG
Korean Journal of Urology 1973;14(2):105-108
Ureteroceles can be classified as intravesical forms which terminate inside the vesical cavity and ectopic ones which terminate in the vesical outlet, urethra, or elsewhere. Most intravesical ureteroceles do not require operative intervention, except when they are obstructive because of harboring calculi, upper tract dilation or infection, and when the function of the intramural portion of the ureter appears irreparably injured. Two cases of intravesical ureterocele including a calculus, occurring in female patients, 27 and 37 years old. are presented with a brief review of the literature.
Adult
;
Calculi*
;
Female
;
Humans
;
Ureter
;
Ureterocele*
;
Urethra
9.A Case of Bilateral Ureterocele.
Korean Journal of Urology 1969;10(1):17-19
A case of bilateral ureterocele developed in the 23 years old Korean male soldier was presented with review of literatures. It was not accompanied any secondary complications and the treatment was conservative rather than surgical intervention.
Humans
;
Male
;
Military Personnel
;
Ureterocele*
;
Young Adult
10.A Case of Uncrossed Complete Ureteral Duplication with Upper System Reflux and Caudal Orthotopic Orifice with Ureterocele.
Dai Haing CHO ; Kwang Don LEE ; Suk Young JUNG ; Sung Hak KANG ; Jong Hoon AHN ; Dong Hwan LEE
Korean Journal of Urology 1994;35(6):686-689
We report a case of uncrossed complete ureteral duplication with the orifice of the upper system ureter opening in the cranial and lateral positionin the bladder. There was reflux only to the upper system of the duplex kidney and the orifice of the lower system ureter in caudal position was associated with a ureterocele, and the lower pole system was large and non-functioning. The patient was treated successfully by lower pole heminephrectomy and ureterectomy.
Humans
;
Kidney
;
Ureter*
;
Ureterocele*
;
Urinary Bladder