An unusual case of complete bladder duplication without ureteric connection

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Complete duplication of bladder and urethra: a case report.

A case of complete duplication of the bladder and urethra in a girl is reported, demonstrating outlet obstruction in the bladder on the left side. Associated anomalies and pertinent literature are reviewed.

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An unusual cause of diffuse ascites in an infant: colonic duplication associated with bladder duplication.

Colonic duplication is usually asymptomatic; however, when it is symptomatic, patients with this anomaly may present with bleeding, constipation, or manifestations of obstruction, perforation, or malignancy. We report the case of a sixteen-month-old boy who presented with diffuse ascites, and had complete colonic duplication and bladder duplication. Duplication of the colon associated with blad...

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Novel Presentation of Complete Coronal Urethral Duplication: a Case Report

     Urethralduplication is a rare condition occurs as a congenital malformation either independently or in the setting of other congenital malformations such as caudal duplication syndrome. Its prevalence becomes even rarer if it manifests as two side-by-side tracts in coronal plan.Nonetheless, we introduce a unique presentation of complete coronal urethral duplication accompanied by astoundin...

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Percutaneous nephrostomy in an unusual case of ureteric obstruction.

Ureteric obstruction from an iliac artery aneurysm is uncommon.1 We report what we believe to be the first case in which percutaneous nephrostomy was used in the management. CASE REPORT A 70-year-old man presented with rigors. He had a history of severe cardiovascular disease. Examination revealed marked congestive cardiac failure, a palpable abdominal aortic aneurysm and a separate pulsatile m...

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First Case of Complete Bladder Duplication in the Coronal Plane with Concomitant Duplication of the Urethra in an Adult Male

Duplication of the lower urinary tract is a very rare congenital anomaly which is diagnosed either at birth or during early childhood. These rare malformations are most of the times accompanied by other concomitant anomalies and are therefore diagnosed immediately after birth. In some even rarer cases there are no concomitant anomalies and symptoms thus leading to a diagnosis later in childhood...

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ژورنال

عنوان ژورنال: Journal of Pediatric Urology

سال: 2020

ISSN: 1477-5131

DOI: 10.1016/j.jpurol.2020.05.091