Blind-Ending Bifid Ureters - Report of Five Pediatric Cases

Alessandrini, P.; Derlon, S; Hajj, Maher

doi:10.1159/000474868

Cited by 3 publications

(5 citation statements)

References 8 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Some authors claim that a cap of nephrogenic tissue representing the remnant of the metanephric blastema ( 6 , 7 ) or a fibrous band connecting the upper blind extremity with a metanephric remnant ( 3 ) may be present, while others have not reported such observations ( 8 ) .…”

Section: Discussionmentioning

confidence: 99%

“…Blind-ending bifid ureter may cause complications such as abdominal pain, hematuria ( 1 ) and recurrent urinary tract infections ( 3 ) . Ureterolithiasis ( 9 ) or even transitional cell carcinoma ( 10 ) might develop in the blind-ending branch.…”

Section: Discussionmentioning

confidence: 99%

“…It appears that the condition is more frequent in women and affects predominantly the right side ( 2 ) . Most cases were diagnosed with intravenous or retrograde pyelography ( 3 ) , computed tomography (CT) urography ( 1 ) or ureteroscopy ( 2 ) .…”

Section: Introductionmentioning

confidence: 99%

See 2 more Smart Citations

Blind-ending bifid ureter – a case report of rare congenital anomaly and its sonographic appearance

Łyczek¹,

Migda²

2022

J Ultrason

View full text Add to dashboard Cite

Aim of the study: We report a case of a blind-ending bifid ureter in a 67-year-old woman with ascites initially diagnosed with B-mode and Color Doppler ultrasonography and afterwards verified with contrast-enhanced abdominal computed tomography. A literature review of the pathogenesis, sonographic appearance with differential diagnoses and clinical significance is also presented and discussed. Case description: The patient was referred for an abdominal ultrasound due to enlarged abdomen circumference. Ultrasound revealed signs of chronic pancreatitis with cavernous transformation of the portal vein and large ascites resulting in bilateral pelvicalyceal system dilatation. Additionally, we have preliminarily diagnosed right-sided, dilatated blind-ending bifid ureter with associated contralateral complete duplication of the ureter and the collecting system. These findings, initially revealed with ultrasound, were confirmed with contrast-enhanced abdominal computed tomography. Conclusions: To our knowledge, this is the first detailed description of sonographic appearance of blind-ending bifid ureter.

show abstract

Section: Discussionmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

See 1 more Smart Citation

Blind-ending bifid ureter – a case report of rare congenital anomaly and its sonographic appearance

Łyczek¹,

Migda²

2022

J Ultrason

View full text Add to dashboard Cite

show abstract

“…Alessandrini reported 5 cases of pediatric ureter blind ending; all diagnosed by cystography and he said that this examination should be performed in the first step of investigation of urinary tract in children [ 8 ]. Abdominal CT shows when it's a hernia of the intestine which is the most frequent, an agglutination of the small intestine with the air-fluid levels in the pelvic cavity.…”

Section: Discussionmentioning

confidence: 99%

Hernia of the bladder through the broad ligament with renal agenesis and ipsilateral ureter blind ending

Madi¹,

Khattala²,

Rami³

et al. 2014

Pan Afr Med J

View full text Add to dashboard Cite

Hernia through a defect of the broad ligament is extremely rare in children. These defects can result from a developmental defect or a spontaneous rupture of cystic formations remnants of mesonephric ducts or Müller. Genital anomalies associated with unilateral renal agenesis are more common in females. We report the case of a 13 months girl allowed for assessment of recurrent urinary tract infection; abdominal examination did not objectified palpable mass, the external genitalia were without abnormalities. Abdominal ultrasound revealed a left renal space is empty with a retrovesical cyst. Cystography was requested that objectified a large pelvic cystic mass retrovesical communicating with the bladder, there was also a left vesicoureteral reflux. Uro- MRI showed a cystic formation retrovesical communicating with the bladder, the right pelvic kidney; uterus is normal size for age. DMSA scintigraphy confirmed the absence of the left kidney with the right kidney that ensures 100% of total renal function. To surgical exploration we found a hernia of the bladder through the left broad ligament, the uterus was dislocated on the right side; left ovary was hypoplasic; the ipsilateral ureter was blind with renal agenesis, we performed by reduction of the bladder then closing the hernial orifice, dissection of the ureter with its ligation and section at the vesical stoma. The postoperative course was uneventful. Evolution is favorable. This observation illustrates a hernia of the bladder through the broad ligament associated with ovarian hypoplasia, renal agenesis and ipsilateral ureter blind ending; this association was not described to our knowledge in the literature.

show abstract

“…Reflux may explain the common problem of loin pain and is responsible for the development of infection and calcu lus formation. Alessandrini et al [17] reported vesicoure teral reflux in 5 cases.…”

Section: Discussionmentioning

confidence: 99%

Urolithiasis with Blind-Ending Ureteral Duplication and Azotemia Treated with Shock Wave Therapy

Bhatia¹,

Biyani²

1993

Urol Int

View full text Add to dashboard Cite

A case of bilateral urolithiasis and renal insufficiency with a blind-ending branch of the right bifid ureter is presented. The diagnosis was made by retrograde ureterogram which revealed a blind-ending branch originating in the middle third of the right ureter. Stones were treated with phased extracorporeal shock wave lithotripsy after preliminary bilateral JJ stenting. The renal parameters reverted to normal and the patient was stone-free.

show abstract

Blind-Ending Bifid Ureters - Report of Five Pediatric Cases

Cited by 3 publications

References 8 publications

Blind-ending bifid ureter – a case report of rare congenital anomaly and its sonographic appearance

Blind-ending bifid ureter – a case report of rare congenital anomaly and its sonographic appearance

Hernia of the bladder through the broad ligament with renal agenesis and ipsilateral ureter blind ending

Urolithiasis with Blind-Ending Ureteral Duplication and Azotemia Treated with Shock Wave Therapy

Contact Info

Product

Resources

About