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Article Synopsis
  • Ectopic ureteroceles are rare in adults but often found in children, typically discovered during pregnancy ultrasounds or through UTI symptoms.
  • A 24-year-old woman faced recurrent UTIs and severe urinary retention due to a large ectopic ureterocele, confirmed through imaging and cystoscopy.
  • The minimally invasive treatment led to her full recovery and emphasizes the need to consider ectopic ureteroceles in adult women with frequent urinary issues.
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Article Synopsis
  • A ureterocele is a congenital defect where the lower part of the ureter becomes abnormally enlarged as it enters the bladder.
  • Patients commonly experience issues like frequent urinary tract infections, urinary retention, abdominal pains, trouble gaining weight, and blood in urine.
  • The case discusses a 51-year-old woman with recurrent UTIs who was diagnosed with bilateral ureteroceles through various imaging techniques.
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Article Synopsis
  • Ureterocele is a rare congenital condition where the distal part of the ureter dilates, often seen in children but can occur in adults, leading to complications like prolapse and stone formation.
  • A 19-year-old female was diagnosed with a prolapsed ureterocele and a stone during imaging, which led to endoscopic resection to treat the issue.
  • Post-surgery, the patient remained symptom-free for a year, indicating that endoscopic treatment is effective in preventing recurring prolapse in these cases.
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Background: Endoscopic transurethral electro-incision and resection are minimally invasive options for treating adult single system ureterocoele. Vesicoureteral (VU) reflux is frequently associated with ureterocoeles and can complicate the treatment. The literature on endoscopic management isscanty from sub-Saharan Africa.

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[Ureterocele associated with simplex ureter in children: clinical and therapeutic features].

Pan Afr Med J

August 2021

Service de Chirurgie Pédiatrique, Hôpital Fattouma Bourguiba de Monastir, Monastir, Tunisie.

Ureterocele is a pseudo-cyst dilation of the terminal submucosal ureter. It is a rare malformative uropathy, in particular associated with simplex ureter. We conducted a retrospective study over a period of 10 years.

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