Cargando…

Duplex Kidney Anomalies and Associated Pathologies in Children: A Single-Center Retrospective Review

Introduction: 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...

Descripción completa

Detalles Bibliográficos
Autores principales: Yener, Sevim, Pehlivanoğlu, Cemile, Akis Yıldız, Zeliha, Ilce, Huri T, Ilce, Zekeriya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9270195/
https://www.ncbi.nlm.nih.gov/pubmed/35812643
http://dx.doi.org/10.7759/cureus.25777
_version_ 1784744407661019136
author Yener, Sevim
Pehlivanoğlu, Cemile
Akis Yıldız, Zeliha
Ilce, Huri T
Ilce, Zekeriya
author_facet Yener, Sevim
Pehlivanoğlu, Cemile
Akis Yıldız, Zeliha
Ilce, Huri T
Ilce, Zekeriya
author_sort Yener, Sevim
collection PubMed
description Introduction: 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. Methods: 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. Results: 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. Conclusions: 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.
format Online
Article
Text
id pubmed-9270195
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Cureus
record_format MEDLINE/PubMed
spelling pubmed-92701952022-07-09 Duplex Kidney Anomalies and Associated Pathologies in Children: A Single-Center Retrospective Review Yener, Sevim Pehlivanoğlu, Cemile Akis Yıldız, Zeliha Ilce, Huri T Ilce, Zekeriya Cureus Pediatric Surgery Introduction: 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. Methods: 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. Results: 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. Conclusions: 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. Cureus 2022-06-09 /pmc/articles/PMC9270195/ /pubmed/35812643 http://dx.doi.org/10.7759/cureus.25777 Text en Copyright © 2022, Yener et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Pediatric Surgery
Yener, Sevim
Pehlivanoğlu, Cemile
Akis Yıldız, Zeliha
Ilce, Huri T
Ilce, Zekeriya
Duplex Kidney Anomalies and Associated Pathologies in Children: A Single-Center Retrospective Review
title Duplex Kidney Anomalies and Associated Pathologies in Children: A Single-Center Retrospective Review
title_full Duplex Kidney Anomalies and Associated Pathologies in Children: A Single-Center Retrospective Review
title_fullStr Duplex Kidney Anomalies and Associated Pathologies in Children: A Single-Center Retrospective Review
title_full_unstemmed Duplex Kidney Anomalies and Associated Pathologies in Children: A Single-Center Retrospective Review
title_short Duplex Kidney Anomalies and Associated Pathologies in Children: A Single-Center Retrospective Review
title_sort duplex kidney anomalies and associated pathologies in children: a single-center retrospective review
topic Pediatric Surgery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9270195/
https://www.ncbi.nlm.nih.gov/pubmed/35812643
http://dx.doi.org/10.7759/cureus.25777
work_keys_str_mv AT yenersevim duplexkidneyanomaliesandassociatedpathologiesinchildrenasinglecenterretrospectivereview
AT pehlivanoglucemile duplexkidneyanomaliesandassociatedpathologiesinchildrenasinglecenterretrospectivereview
AT akisyıldızzeliha duplexkidneyanomaliesandassociatedpathologiesinchildrenasinglecenterretrospectivereview
AT ilcehurit duplexkidneyanomaliesandassociatedpathologiesinchildrenasinglecenterretrospectivereview
AT ilcezekeriya duplexkidneyanomaliesandassociatedpathologiesinchildrenasinglecenterretrospectivereview