Adult ureteroceles are generally known as simple ureteroceles with minimal obstructive effects 1 that can usually be managed endoscopically. Such pathology presented with acute abdominal pain and fever in a 32-year-old man with left renal agenesia, a cranial blind left ureter and left obstructed ureterocele. The retained secretions were suppurative.

Urethral doubling is a rare congenital malformation of the lower urinary tract. A little more than 200 cases various forms this defect have been described in literature worldwide. We present clinical case duplication urethra combination with megaureter only functioning kidney. In patient, we encountered previously undescribed anomaly within generally accepted classification kidney collecting sy...

An analysis of 5 patients with an acquired dilatation of the distal ureter, simulating a simple ureterocele, is herein reported. Radiologically, pseudoureteroceles are more likely to be associated with ipsilateral upper tract obstruction and have asymmetric intravesical dilatation. The urologist should be aware of this urographic deformity, for the majority of pseudoureteroceles are related to ...

We report the fifth case in the English literature of a horseshoe kidney with a complete ureteral duplication. Our case is unique in that the previous four cases occurred in the presence of a ureterocele, whereas our patient lacked this anomaly. Further, our patient was managed conservatively, whereas the previous four patients were managed with surgery.

Urinary collecting system duplication is a congenital anomaly and can associate various types of urinary tract pathologies. Authors will illustrate by cases some of associated anomalies such as ureterocele, extravesical ectopic ureter, vesicoureteral reflux or reflux nephropathy; one case presented an association between posterior urethral valve and bilateral collecting system duplication.

adult ureteroceles are generally known as simple ureteroceles with minimal obstructive effects 1 that can usually be managed endoscopically. such pathology presented with acute abdominal pain and fever in a 32-year-old man with left renal agenesia, a cranial blind left ureter and left obstructed ureterocele. the retained secretions were suppurative.