Duplicated collecting system with ectopic vaginal implantation
We present a case of a 54-year-old woman with a left-sided complete duplication of the ureter. The upper moiety drains in the proximal third of the vagina, which results in an ureterocele and urinary incontinence. The ureteral orifice of lower moiety ureter was normal. Duplication of the ureters wit...
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creator | Behaeghe, Maxim Seynaeve, Patrick Verstraete, Koenraad |
description | We present a case of a 54-year-old woman with a left-sided complete duplication of the ureter. The upper moiety drains in the proximal third of the vagina, which results in an ureterocele and urinary incontinence. The ureteral orifice of lower moiety ureter was normal. Duplication of the ureters with distal, infrasphincteric, vaginal implantation is an uncommon congenital anomaly and a rarely seen entity in adulthood as a cause of urinary incontinence. MR colpocystodefecography showed an ureterocele in between the bladder and the rectum. Computed-tomography showed the duplicated ureters and ectopic ureter with proximal implantation on the renal upper pole and distal implantation on the proximal third of the vagina. |
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The upper moiety drains in the proximal third of the vagina, which results in an ureterocele and urinary incontinence. The ureteral orifice of lower moiety ureter was normal. Duplication of the ureters with distal, infrasphincteric, vaginal implantation is an uncommon congenital anomaly and a rarely seen entity in adulthood as a cause of urinary incontinence. MR colpocystodefecography showed an ureterocele in between the bladder and the rectum. Computed-tomography showed the duplicated ureters and ectopic ureter with proximal implantation on the renal upper pole and distal implantation on the proximal third of the vagina.</description><identifier>ISSN: 2514-8281</identifier><identifier>EISSN: 2514-8281</identifier><language>eng</language><subject>Complete duplication ; Duplicated collecting system ; Ectopic ureter ; Ectopic vaginal implantation ; Incontinence ; INSERTION ; Medicine and Health Sciences ; Reflux ; URETERAL DUPLICATION ; Ureterocele</subject><creationdate>2018</creationdate><rights>Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) info:eu-repo/semantics/openAccess</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,776,780,27839</link.rule.ids></links><search><creatorcontrib>Behaeghe, Maxim</creatorcontrib><creatorcontrib>Seynaeve, Patrick</creatorcontrib><creatorcontrib>Verstraete, Koenraad</creatorcontrib><title>Duplicated collecting system with ectopic vaginal implantation</title><description>We present a case of a 54-year-old woman with a left-sided complete duplication of the ureter. The upper moiety drains in the proximal third of the vagina, which results in an ureterocele and urinary incontinence. The ureteral orifice of lower moiety ureter was normal. Duplication of the ureters with distal, infrasphincteric, vaginal implantation is an uncommon congenital anomaly and a rarely seen entity in adulthood as a cause of urinary incontinence. MR colpocystodefecography showed an ureterocele in between the bladder and the rectum. Computed-tomography showed the duplicated ureters and ectopic ureter with proximal implantation on the renal upper pole and distal implantation on the proximal third of the vagina.</description><subject>Complete duplication</subject><subject>Duplicated collecting system</subject><subject>Ectopic ureter</subject><subject>Ectopic vaginal implantation</subject><subject>Incontinence</subject><subject>INSERTION</subject><subject>Medicine and Health Sciences</subject><subject>Reflux</subject><subject>URETERAL DUPLICATION</subject><subject>Ureterocele</subject><issn>2514-8281</issn><issn>2514-8281</issn><fulltext>true</fulltext><rsrctype>web_resource</rsrctype><creationdate>2018</creationdate><recordtype>web_resource</recordtype><sourceid>ADGLB</sourceid><recordid>eNqdjE0OgjAUhBujiUS5Qy9AAihQN278iQdw3zzqszxTWkILxtuLiQvXrmbyTb6ZsSgvsm0icpHNf_qSxd4_0jTNRJkXOxGx_XHoDCkIeOPKGYMqkNXcv3zAlj8pNHxCriPFR9BkwXBqOwM2QCBn12xxB-Mx_uaK5efT9XBJdIM2SEN1j9O5dEASetXQiHLQn6lGKYqqrMRm85f0BrwkR_Y</recordid><startdate>2018</startdate><enddate>2018</enddate><creator>Behaeghe, Maxim</creator><creator>Seynaeve, Patrick</creator><creator>Verstraete, Koenraad</creator><scope>ADGLB</scope></search><sort><creationdate>2018</creationdate><title>Duplicated collecting system with ectopic vaginal implantation</title><author>Behaeghe, Maxim ; Seynaeve, Patrick ; Verstraete, Koenraad</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-ghent_librecat_oai_archive_ugent_be_85767833</frbrgroupid><rsrctype>web_resources</rsrctype><prefilter>web_resources</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Complete duplication</topic><topic>Duplicated collecting system</topic><topic>Ectopic ureter</topic><topic>Ectopic vaginal implantation</topic><topic>Incontinence</topic><topic>INSERTION</topic><topic>Medicine and Health Sciences</topic><topic>Reflux</topic><topic>URETERAL DUPLICATION</topic><topic>Ureterocele</topic><toplevel>online_resources</toplevel><creatorcontrib>Behaeghe, Maxim</creatorcontrib><creatorcontrib>Seynaeve, Patrick</creatorcontrib><creatorcontrib>Verstraete, Koenraad</creatorcontrib><collection>Ghent University Academic Bibliography</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Behaeghe, Maxim</au><au>Seynaeve, Patrick</au><au>Verstraete, Koenraad</au><format>book</format><genre>unknown</genre><ristype>GEN</ristype><btitle>Duplicated collecting system with ectopic vaginal implantation</btitle><date>2018</date><risdate>2018</risdate><issn>2514-8281</issn><eissn>2514-8281</eissn><abstract>We present a case of a 54-year-old woman with a left-sided complete duplication of the ureter. The upper moiety drains in the proximal third of the vagina, which results in an ureterocele and urinary incontinence. The ureteral orifice of lower moiety ureter was normal. Duplication of the ureters with distal, infrasphincteric, vaginal implantation is an uncommon congenital anomaly and a rarely seen entity in adulthood as a cause of urinary incontinence. MR colpocystodefecography showed an ureterocele in between the bladder and the rectum. Computed-tomography showed the duplicated ureters and ectopic ureter with proximal implantation on the renal upper pole and distal implantation on the proximal third of the vagina.</abstract><oa>free_for_read</oa></addata></record> |
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source | DOAJ Directory of Open Access Journals; PubMed Central Open Access; Ghent University Academic Bibliography; Ubiquity Partner Network Journals (Open Access); PubMed Central |
subjects | Complete duplication Duplicated collecting system Ectopic ureter Ectopic vaginal implantation Incontinence INSERTION Medicine and Health Sciences Reflux URETERAL DUPLICATION Ureterocele |
title | Duplicated collecting system with ectopic vaginal implantation |
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