To investigate the presentation and management of ureteroceles remaining asymptomatic until adulthood. A ureterocele is a congenital cystic dilation of the distal ureter upon its entry point into the bladder. This birth defect obstructs urine flow and can negatively impact proper renal function. Treatment options vary widely depending on the type of ureterocele and the presence or absence of a duplicated collecting system. We present a rare case of a 59-year-old female with a symptomatic left intravesical single system ureterocele successfully managed with endoscopic resection. Ureteroceles are commonly diagnosed in utero or within the first few years of life. However, primarily due to her asymptomatic nature until nearly 60 years of age, our patient offers an unusual presentation of a ureterocele diagnosed initially in adulthood. Various classification systems are employed in the diagnosis of ureteroceles, however the Ericsson and Glassberg classification systems are most widely used. A duplex kidney is a common finding in ureterocele cases and typically necessitates a more complex treatment plan. The management of ureteroceles varies based on classification, presence of symptoms, age, severity, and concurrent complications. As seen with our patient, a significant symptomatic presentation may warrant surgical intervention via endoscopic resection of the ureterocele. Ureteroceles can be managed using conservative treatment or surgical intervention via endoscopic resection, as seen in our patient. If surgical intervention is pursued, patients should be continually monitored for postoperative complications including hydronephrosis and urinary tract infections.
| Published in | International Journal of Clinical Urology (Volume 6, Issue 2) |
| DOI | 10.11648/j.ijcu.20220602.17 |
| Page(s) | 114-118 |
| Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
| Copyright |
Copyright © The Author(s), 2022. Published by Science Publishing Group |
Ureterocele, Case Report, Asymptomatic, Urology, Orthotopic
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APA Style
Sarah Johnson, Samuel Huff, Thomas Barefoot, Kellen Choi. (2022). Symptomatic Ureterocele in 59-Year-Old Woman: Surgical Management of Adult Ureterocele. International Journal of Clinical Urology, 6(2), 114-118. https://doi.org/10.11648/j.ijcu.20220602.17
ACS Style
Sarah Johnson; Samuel Huff; Thomas Barefoot; Kellen Choi. Symptomatic Ureterocele in 59-Year-Old Woman: Surgical Management of Adult Ureterocele. Int. J. Clin. Urol. 2022, 6(2), 114-118. doi: 10.11648/j.ijcu.20220602.17
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Download@article{10.11648/j.ijcu.20220602.17,
author = {Sarah Johnson and Samuel Huff and Thomas Barefoot and Kellen Choi},
title = {Symptomatic Ureterocele in 59-Year-Old Woman: Surgical Management of Adult Ureterocele},
journal = {International Journal of Clinical Urology},
volume = {6},
number = {2},
pages = {114-118},
doi = {10.11648/j.ijcu.20220602.17},
url = {https://doi.org/10.11648/j.ijcu.20220602.17},
eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijcu.20220602.17},
abstract = {To investigate the presentation and management of ureteroceles remaining asymptomatic until adulthood. A ureterocele is a congenital cystic dilation of the distal ureter upon its entry point into the bladder. This birth defect obstructs urine flow and can negatively impact proper renal function. Treatment options vary widely depending on the type of ureterocele and the presence or absence of a duplicated collecting system. We present a rare case of a 59-year-old female with a symptomatic left intravesical single system ureterocele successfully managed with endoscopic resection. Ureteroceles are commonly diagnosed in utero or within the first few years of life. However, primarily due to her asymptomatic nature until nearly 60 years of age, our patient offers an unusual presentation of a ureterocele diagnosed initially in adulthood. Various classification systems are employed in the diagnosis of ureteroceles, however the Ericsson and Glassberg classification systems are most widely used. A duplex kidney is a common finding in ureterocele cases and typically necessitates a more complex treatment plan. The management of ureteroceles varies based on classification, presence of symptoms, age, severity, and concurrent complications. As seen with our patient, a significant symptomatic presentation may warrant surgical intervention via endoscopic resection of the ureterocele. Ureteroceles can be managed using conservative treatment or surgical intervention via endoscopic resection, as seen in our patient. If surgical intervention is pursued, patients should be continually monitored for postoperative complications including hydronephrosis and urinary tract infections.},
year = {2022}
}
TY - JOUR T1 - Symptomatic Ureterocele in 59-Year-Old Woman: Surgical Management of Adult Ureterocele AU - Sarah Johnson AU - Samuel Huff AU - Thomas Barefoot AU - Kellen Choi Y1 - 2022/11/04 PY - 2022 N1 - https://doi.org/10.11648/j.ijcu.20220602.17 DO - 10.11648/j.ijcu.20220602.17 T2 - International Journal of Clinical Urology JF - International Journal of Clinical Urology JO - International Journal of Clinical Urology SP - 114 EP - 118 PB - Science Publishing Group SN - 2640-1355 UR - https://doi.org/10.11648/j.ijcu.20220602.17 AB - To investigate the presentation and management of ureteroceles remaining asymptomatic until adulthood. A ureterocele is a congenital cystic dilation of the distal ureter upon its entry point into the bladder. This birth defect obstructs urine flow and can negatively impact proper renal function. Treatment options vary widely depending on the type of ureterocele and the presence or absence of a duplicated collecting system. We present a rare case of a 59-year-old female with a symptomatic left intravesical single system ureterocele successfully managed with endoscopic resection. Ureteroceles are commonly diagnosed in utero or within the first few years of life. However, primarily due to her asymptomatic nature until nearly 60 years of age, our patient offers an unusual presentation of a ureterocele diagnosed initially in adulthood. Various classification systems are employed in the diagnosis of ureteroceles, however the Ericsson and Glassberg classification systems are most widely used. A duplex kidney is a common finding in ureterocele cases and typically necessitates a more complex treatment plan. The management of ureteroceles varies based on classification, presence of symptoms, age, severity, and concurrent complications. As seen with our patient, a significant symptomatic presentation may warrant surgical intervention via endoscopic resection of the ureterocele. Ureteroceles can be managed using conservative treatment or surgical intervention via endoscopic resection, as seen in our patient. If surgical intervention is pursued, patients should be continually monitored for postoperative complications including hydronephrosis and urinary tract infections. VL - 6 IS - 2 ER -
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