Case of Incomplete Ureteral Duplication Complicated with Lithiasis and Right Uretero-Hydronephrosis  

作　　者：Cheickna Tounkara Amadou Maiga Boubacar Yoro Sidibe Tani Kone Samake Hamidou Kaloga Daye Bagayoko Oumar Amadou Malle Jean Batiste Honoré Berthe Mamadou Lamine Diakite Cheickna Tounkara;Amadou Maiga;Boubacar Yoro Sidibe;Tani Kone;Samake Hamidou;Kaloga Daye Bagayoko;Oumar Amadou Malle;Jean Batiste Honoré Berthe;Mamadou Lamine Diakite(Department of General Surgery, Luxembourg Hospital, Bamako, Mali;Department of General Surgery, CHU Gabriel Touré, Bamako Mali;Department of Urology Surgery, CHU Point-G, Bamako, Mali)

机构地区：[1]Department of General Surgery, Luxembourg Hospital, Bamako, Mali [2]Department of General Surgery, CHU Gabriel Touré, Bamako Mali [3]Department of Urology Surgery, CHU Point-G, Bamako, Mali

出　　处：《Surgical Science》2023年第7期502-506,共5页外科学（英文）

摘　　要：Ureteral duplication is congenital malformative uropathy that occurs most often in children. Complete ureteral duplication is defined by a kidney that has two ureters with two orifices that communicate to the bladder through two ureteral meati. It is an anatomical variant that remains rare. Its early discovery is due to a lack of diagnostic means, hence the occurrence of long-term complications. To this end, we observe an increased importance of the morbidity linked to the late diagnosis of this duplicity. We report a case of incomplete ureteral duplication complicated by ureterohydronephrosis on lithiasis wedged in the uretero-vesical junction of one of the ureters in its lower portion which required uretero-lithotomy with bladder reimplantation of the ureters. Our aim was to show the importance of the morbidity associated with late diagnosis of this anomaly and the incidence of infection and complications that this pathology poses as a problem. This was a clinical case of fortuitous discovery managed by a general surgeon in the general surgery department of the hospital “Mère Enfant” Le Luxembourg Bamako Mali. The suites were simple.Ureteral duplication is congenital malformative uropathy that occurs most often in children. Complete ureteral duplication is defined by a kidney that has two ureters with two orifices that communicate to the bladder through two ureteral meati. It is an anatomical variant that remains rare. Its early discovery is due to a lack of diagnostic means, hence the occurrence of long-term complications. To this end, we observe an increased importance of the morbidity linked to the late diagnosis of this duplicity. We report a case of incomplete ureteral duplication complicated by ureterohydronephrosis on lithiasis wedged in the uretero-vesical junction of one of the ureters in its lower portion which required uretero-lithotomy with bladder reimplantation of the ureters. Our aim was to show the importance of the morbidity associated with late diagnosis of this anomaly and the incidence of infection and complications that this pathology poses as a problem. This was a clinical case of fortuitous discovery managed by a general surgeon in the general surgery department of the hospital “Mère Enfant” Le Luxembourg Bamako Mali. The suites were simple.

关 键 词：Ureteral Duplication Congenital Malformation Adult 

分 类 号：R73[医药卫生—肿瘤]