Single system ectopic ureters: Adult presentation of a congenital anomaly

Objective:: To retrospectively review a cohort of adult patients with single ectopic ureter, a rare congenital abnormality where one ureter terminates in an abnormal position outside of the trigone of the bladder. Methods:: We identified 5 patients diagnosed with a single ectopic ureter over a singl...

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Main Authors: Mahyar Kashani, Abdo E. Kabarriti, Neeta D’Souza, Jeffrey P. Weiss
Format: Article
Language:English
Published: Elsevier 2022-03-01
Series:Continence
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S277297372200008X
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author Mahyar Kashani
Abdo E. Kabarriti
Neeta D’Souza
Jeffrey P. Weiss
author_facet Mahyar Kashani
Abdo E. Kabarriti
Neeta D’Souza
Jeffrey P. Weiss
author_sort Mahyar Kashani
collection DOAJ
description Objective:: To retrospectively review a cohort of adult patients with single ectopic ureter, a rare congenital abnormality where one ureter terminates in an abnormal position outside of the trigone of the bladder. Methods:: We identified 5 patients diagnosed with a single ectopic ureter over a single surgeon’s career over 35 years and 2 institutions. Clinical symptoms, medical history, interventions, available radiologic imaging, and urodynamic features were analyzed. Results:: Median age at diagnosis was 53 years (range 18–85 years). The majority were male (80%). All patients were noted to have a solitary functioning kidney. A diminutive contralateral kidney and ureter was found in 1 (20%) patient. All patients were symptomatic, with the most common presenting symptoms being chronic dysuria (60%) and chronic prostatitis (40%). Physical examination findings were identified in 3 (60%) patients. Interventions were principally dependent upon the type and severity of each patient’s symptoms, and included observation, drainage of ectopic structures, vaginal marsupialization, and laparoscopic nephroureterectomy. The 3 (60%) patients that underwent intervention remained symptom free and the 2 (40%) patients that decided on observation were minimally symptomatic. Conclusions:: Single ectopic ureter is a complex embryological abnormality that can result in a wide array of anatomic variations and clinical findings in both men and women. Given the rarity of this entity in adult patients, a high index of suspicion must be held by the clinician for this diagnosis. Ultimately, treatment options for these patients will be dependent upon symptom severity, anatomic presentation, and patient quality of life.
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spelling doaj.art-3eadc8c996a142a5bbbcaa946fc9acdb2022-12-22T00:21:34ZengElsevierContinence2772-97372022-03-011100016Single system ectopic ureters: Adult presentation of a congenital anomalyMahyar Kashani0Abdo E. Kabarriti1Neeta D’Souza2Jeffrey P. Weiss3Department of Urology, SUNY Downstate Health Sciences University, Brooklyn, NY, United States of AmericaDepartment of Urology, SUNY Downstate Health Sciences University, Brooklyn, NY, United States of AmericaSUNY Downstate College of Medicine, Brooklyn, NY, United States of AmericaDepartment of Urology, SUNY Downstate Health Sciences University, Brooklyn, NY, United States of America; VA New York Harbor Healthcare System, Brooklyn, NY, United States of America; Correspondence to: Department of Urology, SUNY Downstate Health Sciences University, 445 Lenox Road, Brooklyn, NY 11203, United States of America.Objective:: To retrospectively review a cohort of adult patients with single ectopic ureter, a rare congenital abnormality where one ureter terminates in an abnormal position outside of the trigone of the bladder. Methods:: We identified 5 patients diagnosed with a single ectopic ureter over a single surgeon’s career over 35 years and 2 institutions. Clinical symptoms, medical history, interventions, available radiologic imaging, and urodynamic features were analyzed. Results:: Median age at diagnosis was 53 years (range 18–85 years). The majority were male (80%). All patients were noted to have a solitary functioning kidney. A diminutive contralateral kidney and ureter was found in 1 (20%) patient. All patients were symptomatic, with the most common presenting symptoms being chronic dysuria (60%) and chronic prostatitis (40%). Physical examination findings were identified in 3 (60%) patients. Interventions were principally dependent upon the type and severity of each patient’s symptoms, and included observation, drainage of ectopic structures, vaginal marsupialization, and laparoscopic nephroureterectomy. The 3 (60%) patients that underwent intervention remained symptom free and the 2 (40%) patients that decided on observation were minimally symptomatic. Conclusions:: Single ectopic ureter is a complex embryological abnormality that can result in a wide array of anatomic variations and clinical findings in both men and women. Given the rarity of this entity in adult patients, a high index of suspicion must be held by the clinician for this diagnosis. Ultimately, treatment options for these patients will be dependent upon symptom severity, anatomic presentation, and patient quality of life.http://www.sciencedirect.com/science/article/pii/S277297372200008XUreterKidneyLower urinary tract symptomsEmbryologyCongenital
spellingShingle Mahyar Kashani
Abdo E. Kabarriti
Neeta D’Souza
Jeffrey P. Weiss
Single system ectopic ureters: Adult presentation of a congenital anomaly
Continence
Ureter
Kidney
Lower urinary tract symptoms
Embryology
Congenital
title Single system ectopic ureters: Adult presentation of a congenital anomaly
title_full Single system ectopic ureters: Adult presentation of a congenital anomaly
title_fullStr Single system ectopic ureters: Adult presentation of a congenital anomaly
title_full_unstemmed Single system ectopic ureters: Adult presentation of a congenital anomaly
title_short Single system ectopic ureters: Adult presentation of a congenital anomaly
title_sort single system ectopic ureters adult presentation of a congenital anomaly
topic Ureter
Kidney
Lower urinary tract symptoms
Embryology
Congenital
url http://www.sciencedirect.com/science/article/pii/S277297372200008X
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