Congenital midureteral stenosis in children: a 13-year retrospective study based on data from a large pediatric medical center

Abstract Background Midureteral stenosis is very rare in children and can cause congenital hydronephrosis. We report our experience treating children with congenital midureteral stenosis at our center, focusing on the differences in preoperative diagnosis and treatment compared with other congenital...

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Autores principales: Zhaoyi Meng, Defu Lin, Guannan Wang, Yanchao Qu, Ning Sun
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Publicado: BMC 2021
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spelling oai:doaj.org-article:859964d0948d45eabd2ff1c7a3180c332021-11-14T12:30:57ZCongenital midureteral stenosis in children: a 13-year retrospective study based on data from a large pediatric medical center10.1186/s12894-021-00916-21471-2490https://doaj.org/article/859964d0948d45eabd2ff1c7a3180c332021-11-01T00:00:00Zhttps://doi.org/10.1186/s12894-021-00916-2https://doaj.org/toc/1471-2490Abstract Background Midureteral stenosis is very rare in children and can cause congenital hydronephrosis. We report our experience treating children with congenital midureteral stenosis at our center, focusing on the differences in preoperative diagnosis and treatment compared with other congenital obstructive uropathies. Methods We retrospectively reviewed the medical records of 26 children diagnosed with congenital midureteral stenosis at our center between January 2007 and December 2020, such as preoperative examination methods, intraoperative conditions, and postoperative follow-up results. Results Of the 1625 children treated surgically for ureteral narrowing, only 26 (1.6%) were diagnosed with midureteral stenosis, including 15 infants and 11 children. Eighteen (69.2%) were boys, 13 (50%) were affected on the left side, and 23 (88.5%) had isolated ureteral stenosis. Overall, 13 (50%) of the children presented with prenatal hydronephrosis, and 13 (50%) presented with abdominal pain or a mass. All the children had undergone urinary ultrasound and intravenous urography preoperatively; the diagnostic rate of ultrasound was 92.3%. Only 7 (26.9%) children had undergone pyelography. All the children had undergone surgery. The ureteral stenotic segment was less than 1 cm long in 25 (96.2)% of the children. The mean follow-up duration was 22 months (range: 6–50 months). One child developed anastomotic strictures. Urinary tract obstruction was relieved in the other children without long-term complications. Conclusions Congenital midureteral stenosis is rare, accounting for 1.6% of all ureteral obstructions, and its diagnosis is crucial. Urinary ultrasound has a high diagnostic rate and should be the first choice for midureteral stenosis. Retrograde pyelography can be used when the diagnosis is difficult, but routine retrograde pyelography is not recommended. Congenital ureteral stenosis has a relatively short lesion range, largely within 1 cm. The treatment is mainly resection of the stenotic segment and end-to-end ureteral anastomosis, with a good prognosis.Zhaoyi MengDefu LinGuannan WangYanchao QuNing SunBMCarticleMidureteral stenosisHydronephrosisCongenitalObstructionChildrenDiseases of the genitourinary system. UrologyRC870-923ENBMC Urology, Vol 21, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Midureteral stenosis
Hydronephrosis
Congenital
Obstruction
Children
Diseases of the genitourinary system. Urology
RC870-923
spellingShingle Midureteral stenosis
Hydronephrosis
Congenital
Obstruction
Children
Diseases of the genitourinary system. Urology
RC870-923
Zhaoyi Meng
Defu Lin
Guannan Wang
Yanchao Qu
Ning Sun
Congenital midureteral stenosis in children: a 13-year retrospective study based on data from a large pediatric medical center
description Abstract Background Midureteral stenosis is very rare in children and can cause congenital hydronephrosis. We report our experience treating children with congenital midureteral stenosis at our center, focusing on the differences in preoperative diagnosis and treatment compared with other congenital obstructive uropathies. Methods We retrospectively reviewed the medical records of 26 children diagnosed with congenital midureteral stenosis at our center between January 2007 and December 2020, such as preoperative examination methods, intraoperative conditions, and postoperative follow-up results. Results Of the 1625 children treated surgically for ureteral narrowing, only 26 (1.6%) were diagnosed with midureteral stenosis, including 15 infants and 11 children. Eighteen (69.2%) were boys, 13 (50%) were affected on the left side, and 23 (88.5%) had isolated ureteral stenosis. Overall, 13 (50%) of the children presented with prenatal hydronephrosis, and 13 (50%) presented with abdominal pain or a mass. All the children had undergone urinary ultrasound and intravenous urography preoperatively; the diagnostic rate of ultrasound was 92.3%. Only 7 (26.9%) children had undergone pyelography. All the children had undergone surgery. The ureteral stenotic segment was less than 1 cm long in 25 (96.2)% of the children. The mean follow-up duration was 22 months (range: 6–50 months). One child developed anastomotic strictures. Urinary tract obstruction was relieved in the other children without long-term complications. Conclusions Congenital midureteral stenosis is rare, accounting for 1.6% of all ureteral obstructions, and its diagnosis is crucial. Urinary ultrasound has a high diagnostic rate and should be the first choice for midureteral stenosis. Retrograde pyelography can be used when the diagnosis is difficult, but routine retrograde pyelography is not recommended. Congenital ureteral stenosis has a relatively short lesion range, largely within 1 cm. The treatment is mainly resection of the stenotic segment and end-to-end ureteral anastomosis, with a good prognosis.
format article
author Zhaoyi Meng
Defu Lin
Guannan Wang
Yanchao Qu
Ning Sun
author_facet Zhaoyi Meng
Defu Lin
Guannan Wang
Yanchao Qu
Ning Sun
author_sort Zhaoyi Meng
title Congenital midureteral stenosis in children: a 13-year retrospective study based on data from a large pediatric medical center
title_short Congenital midureteral stenosis in children: a 13-year retrospective study based on data from a large pediatric medical center
title_full Congenital midureteral stenosis in children: a 13-year retrospective study based on data from a large pediatric medical center
title_fullStr Congenital midureteral stenosis in children: a 13-year retrospective study based on data from a large pediatric medical center
title_full_unstemmed Congenital midureteral stenosis in children: a 13-year retrospective study based on data from a large pediatric medical center
title_sort congenital midureteral stenosis in children: a 13-year retrospective study based on data from a large pediatric medical center
publisher BMC
publishDate 2021
url https://doaj.org/article/859964d0948d45eabd2ff1c7a3180c33
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