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Related Experiment Videos

[Cecoureterocele. A case report].

H Watanabe, T Hori, S Sasaki

    Nihon Hinyokika Gakkai Zasshi. the Japanese Journal of Urology
    |December 1, 1989
    PubMed
    Summary
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    A rare cecoureterocele in a young girl caused recurrent urinary tract infections. Surgical correction and endoscopic treatment resolved the obstruction and infection.

    Area of Science:

    • Pediatric Urology
    • Congenital Anomalies
    • Urinary Tract Infections

    Context:

    • A 22-month-old girl presented with recurrent urinary tract infections (UTIs), fever, and dysuria.
    • Diagnostic imaging revealed a left duplex kidney with hydroureteronephrosis, reflux into the upper moiety, and bladder outlet obstruction.
    • Endoscopic examination confirmed a cecoureterocele at the bladder neck.

    Purpose:

    • To report a case of cecoureterocele in a pediatric patient.
    • To describe the diagnostic approach and surgical management.
    • To highlight the treatment of residual bladder outlet obstruction.

    Summary:

    • The patient underwent a complex surgical procedure including pyelopyelostomy, ureterectomy, ureterocele resection, and ureteral reimplantation.

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  • Postoperative evaluation identified a remnant cecoureterocele causing persistent bladder outlet obstruction.
  • Endoscopic incision of the remnant successfully relieved the obstruction and resolved the UTIs.

    • Impact:

    • Successful management of a rare congenital anomaly.
    • Demonstrates the effectiveness of a staged surgical and endoscopic approach.
    • Provides insights into the treatment of cecoureterocele and associated complications.