Oshiba Ahmed, Oshiba Samar, Kotb Mostafa, Abouheba Mohamed
Department of Pediatric Surgery, Faculty of Medicine, Alexandria University, Alexandria, 21615, Egypt.
Radio-diagnosis Department, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
BMC Urol. 2025 May 15;25(1):125. doi: 10.1186/s12894-025-01800-z.
Ureteral duplication is one of the most common anomalies affecting the genitourinary system. A broad spectrum of clinical presentations and involvement leads to challenges in diagnosing and treating pediatric urologists. Among the variations commonly encountered are incomplete and complete ureteral duplications with normally developed renal moieties and ureters. In this study, we report our experience regarding this spectrum of anomalies in terms of clinical presentation, workup, and management.
This study was conducted as a single-center retrospective study at our institution from January 2019 to January 2021 on children diagnosed with ureteral duplication anomalies. preliminary renal ultrasonography (RUS) and baseline serum urea and creatinine were done for all patients. This was followed by voiding cystourethrography (VCUG) and magnetic resonance urography (MRU) for anatomical definition as needed and dimercaptosuccinate (DMSA) renal scintigraphy for functional decision.
This study included 28 children diagnosed with renal duplex anomalies. Of our 28 patients, 4 had ectopic obstructing megaureter with dilated upper moiety segment (3 left-sided, 1 right-sided), 6 had lower moiety refluxing ureter (4 left-sided, 2 right-sided), and 3 had refluxing ureter in upper and lower moieties (para-ureteral diverticulum). Lower moiety pelviureteric junction obstruction was diagnosed in only 1 case. 13 cases were diagnosed with ureterocele obstructing the upper moiety segment (9 left-sided, 4 right-sided), of which 2 presented early with dysplastic upper moiety in 1 and dysplastic whole kidney in the other, and 4 were cecoureterocele and prolapsing through bladder neck obstructing the bladder outlet. One duplex system was found to drain in the bladder with a single ureteric opening, indeed a rare anatomical variant (incomplete duplex).
Ureteral duplications, ectopia, and ureteroceles are uncommon, widely variable, and challenging clinical entities. Since there is no standard management protocol, a conservative approach is worth consideration. A thorough, detailed imaging study is key to delineate anatomical variations. Our chosen bottom-to-top approach proved successful in recruiting functional upper-moiety nephrons. Ureteroureterostomy and laparoscopic upper moiety heminephroureterectomy are both safe and feasible procedures in properly selected cases.
Not applicable.
输尿管重复畸形是影响泌尿生殖系统最常见的异常之一。广泛的临床表现和受累情况给小儿泌尿外科医生的诊断和治疗带来挑战。常见的变异包括肾部分和输尿管发育正常的不完全和完全输尿管重复畸形。在本研究中,我们报告了我们在这一系列异常的临床表现、检查和管理方面的经验。
本研究为单中心回顾性研究,于2019年1月至2021年1月在我们机构对诊断为输尿管重复畸形的儿童进行。所有患者均进行了初步肾脏超声检查(RUS)以及基线血清尿素和肌酐检测。随后根据需要进行排尿性膀胱尿道造影(VCUG)和磁共振尿路造影(MRU)以明确解剖结构,并进行二巯基丁二酸(DMSA)肾闪烁显像以做出功能判断。
本研究纳入了28例诊断为肾重复畸形的儿童。在我们的28例患者中,4例有异位梗阻性巨输尿管伴上半部分扩张(3例左侧,1例右侧),6例有下半部分反流性输尿管(4例左侧,2例右侧),3例上下半部分均有反流性输尿管(输尿管旁憩室)。仅1例诊断为下半部分肾盂输尿管连接处梗阻。13例诊断为输尿管囊肿梗阻上半部分(9例左侧,4例右侧),其中2例早期出现上半部分发育不良1例,另1例为全肾发育不良,4例为盲肠输尿管囊肿并经膀胱颈脱垂梗阻膀胱出口。发现1个重复系统通过单一输尿管开口排入膀胱,确实是一种罕见的解剖变异(不完全重复)。
输尿管重复畸形、异位和输尿管囊肿是罕见、变化广泛且具有挑战性的临床实体。由于没有标准的管理方案,保守方法值得考虑。全面、详细的影像学检查是明确解剖变异的关键。我们选择的自下而上的方法在招募功能性上半部分肾单位方面证明是成功的。输尿管输尿管吻合术和腹腔镜上半部分半肾输尿管切除术在适当选择的病例中都是安全可行的手术。
不适用。