Zhao Yijun, Zhu Linfeng, Yang Fan, Chen Guangjie
Department of Urology, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center For Child Health, Hangzhou, 310052, China.
BMC Urol. 2025 May 29;25(1):142. doi: 10.1186/s12894-025-01827-2.
Retroiliac ureter is an extremely rare congenital anomaly, even more rarely accompanied by persisting mesonephric duct and vesicoureteral reflux(VUR). We report such a unique case involving a left inguinal mass that appeared during defecation.
A two-year-old boy presented with a tubular structure resembling a dilated ureter discovered incidentally during open left inguinal hernia repair. Contrast radiography and voiding cystourethrogram(VCUG) revealed a tubular structure in the left groin mimicking a ureter, with grade IV reflux into a branch-shaped left renal pelvis. Three-dimensional CT reconstruction demonstrated a dilated left ureter and a tubular structure distortion, angulation, and depression at the L5-S1 level. Cystoscopy showed the left ureteral orifice near the midline of bladder trigone. Laparoscopic exploration revealed an abnormally deep aortic bifurcation in the left iliac fossa, superior to the left ureter and the tubular structure. The left vas deferens was absent, while the tubular structure traversed the internal ring with the left spermatic vessels and inserted into the distal ipsilateral ureter. Four years later, the patient was readmitted due to decreased left renal function. VCUG persistent left-sided grade IV VUR. Robot-assisted laparoscopic left ureter reimplantation via the Lich-Gregoir technique was conducted, along with resection of the abdominal and inguinal segment of the dilated tubular structure and closure of the ipsilateral internal ring. The tubular structure was ultimately confirmed as an abnormally dilated left vas deferens, and the diagnosis of retroiliac ureter accompanied by persisting mesonephric duct and VUR was made. At the 3-month follow-up, ultrasonography revealed mild hydronephrosis and ureteral dilation of left kidney.
Diagnosing retroiliac ureter with persisting mesonephric duct and VUR is challenging. Although imaging provide critical information, surgical exploration is often required for definitive diagnosis. Treatment involves vas deferens excision and ureteral reimplantation to preserve renal function.
髂后输尿管是一种极其罕见的先天性异常,更罕见的是伴有持续性中肾管和膀胱输尿管反流(VUR)。我们报告了这样一个独特病例,该病例涉及一名在排便时出现的左侧腹股沟肿块。
一名两岁男孩在左侧腹股沟疝开放修补术中偶然发现一个类似扩张输尿管的管状结构。造影和排尿性膀胱尿道造影(VCUG)显示左侧腹股沟有一个类似输尿管的管状结构,伴有四级反流至分支状的左肾盂。三维CT重建显示左侧输尿管扩张,以及在L5 - S1水平处的管状结构扭曲、成角和凹陷。膀胱镜检查显示左侧输尿管口靠近膀胱三角区中线。腹腔镜探查发现左髂窝处主动脉分叉异常深,位于左输尿管和管状结构上方。左侧输精管缺如,而管状结构与左侧精索血管一起穿过内环并插入同侧远端输尿管。四年后,患者因左肾功能下降再次入院。VCUG显示左侧持续性四级VUR。通过Lich - Gregoir技术进行了机器人辅助腹腔镜左侧输尿管再植术,同时切除扩张管状结构的腹部和腹股沟段,并关闭同侧内环。管状结构最终被确认为异常扩张的左侧输精管,诊断为伴有持续性中肾管和VUR的髂后输尿管。在3个月的随访中,超声检查显示左肾轻度肾积水和输尿管扩张。
诊断伴有持续性中肾管和VUR的髂后输尿管具有挑战性。尽管影像学提供了关键信息,但往往需要手术探查才能明确诊断。治疗包括输精管切除和输尿管再植以保留肾功能。