Yener Sevim, Pehlivanoğlu Cemile, Akis Yıldız Zeliha, Ilce Huri T, Ilce Zekeriya
Department of Pediatric Urology, University of Health Sciences Umraniye Training and Research Hospital, Istanbul, TUR.
Department of Pediatric Nephrology, University of Health Sciences Umraniye Training and Research Hospital, Istanbul, TUR.
Cureus. 2022 Jun 9;14(6):e25777. doi: 10.7759/cureus.25777. eCollection 2022 Jun.
Duplex renal collecting systems are one of the most common congenital anomalies of the urinary tract. The exact prevalence of this anomaly is difficult to ascertain because most patients are asymptomatic, and the abnormality is frequently detected incidentally. The aim of this study is to retrospectively review the demographic characteristics and different clinical presentations, related pathology, and treatment methods of patients with duplex system anomaly who applied to our institution, with a literature review.
This is a retrospective study, performed at the Department of Pediatric Urology and Pediatric Surgery, Umraniye Training and Research Hospital, a tertiary center, from 2010 to 2021. Age, gender, presenting symptoms, and associated anomalies were determined in all patients. Asymptomatic patients with variants of duplex kidney anomaly detected incidentally did not require any surgical intervention. Necessary surgical interventions were performed depending on the pathologies of other symptomatic patients associated with duplex kidney anomaly variants.
A total of 239 patients had duplex systems. The patients were divided into two groups according to their age, 0-24 months (newborn and infant) and over 24 months. There were 45 (18.8%) patients in the 1st group and 194 (81.1%) patients in the 2nd group. It was seen that the most common symptom in 85 (35.6%) patients was urinary tract infection (UTI). It was observed that 5 (2%) patients had no symptoms and were detected during routine screening. When comorbidities detected with the duplex system were examined, the most common ones were antenatal hydronephrosis 23 (9.6%). Ureterocele excision was performed in ten patients, laparoscopic heminephrectomy was performed in six patients, and ureteroneocystostomy was performed in one patient.
It is important that magnetic resonance urography (MRU) duplex renal collecting systems, which is a current imaging method used in the evaluation of the duplex system, provide detailed information about the morphology and function and are useful in the evaluation of associated anomalies. Diagnosis and treatment before it becomes symptomatic or results in further kidney damage are important for the preservation of renal function in advanced follow-ups.
重复肾集合系统是最常见的先天性泌尿系统异常之一。由于大多数患者无症状,且该异常常为偶然发现,因此难以确定其确切患病率。本研究旨在回顾性分析我院收治的重复肾系统异常患者的人口统计学特征、不同临床表现、相关病理及治疗方法,并进行文献复习。
本研究为回顾性研究,于2010年至2021年在三级中心乌姆拉尼耶培训与研究医院儿科泌尿外科及小儿外科进行。确定所有患者的年龄、性别、症状表现及合并畸形。偶然发现的无症状重复肾异常变异患者无需任何手术干预。根据其他有症状的合并重复肾异常变异患者的病理情况进行必要的手术干预。
共有239例患者存在重复肾系统。根据年龄将患者分为两组,0 - 24个月(新生儿及婴儿)组和24个月以上组。第一组有45例(18.8%)患者,第二组有194例(81.1%)患者。可见,85例(35.6%)患者最常见的症状为尿路感染(UTI)。观察到5例(2%)患者无症状,在常规筛查中被发现。检查重复肾系统合并的疾病时,最常见的是产前肾积水23例(9.6%)。10例患者行输尿管囊肿切除术,6例患者行腹腔镜半肾切除术,1例患者行输尿管膀胱吻合术。
磁共振尿路造影(MRU)作为目前用于评估重复肾系统的成像方法,对于提供重复肾集合系统的形态和功能详细信息以及评估相关异常非常重要。在出现症状或导致进一步肾损害之前进行诊断和治疗,对于在长期随访中保护肾功能很重要。