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Herlyn-Werner-Wunderlich Syndrome: Sonographic and Magnetic Resonance (MR) Imaging Findings of This Rare Urogenital Anomaly
Herlyn-Werner-Wunderlich syndrome is a rare congenital urogenital anomaly characterised by uterus didelphys with blind hemivagina and ipsilateral renal agenesis. Children usually have progressive pelvic pain after menarche, palpable mass due to hemihaemato(metro)colpos or pelvic inflammatory disease...
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| Published in: | Polish journal of radiology 2017, Vol.82, p.216-219 |
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| Format: | Article |
| Language: | English |
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| container_title | Polish journal of radiology |
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| creator | Yilmaz, Sukriye Yildiz, Adalet Elcin Fitoz, Suat |
| description | Herlyn-Werner-Wunderlich syndrome is a rare congenital urogenital anomaly characterised by uterus didelphys with blind hemivagina and ipsilateral renal agenesis. Children usually have progressive pelvic pain after menarche, palpable mass due to hemihaemato(metro)colpos or pelvic inflammatory disease. The diagnosis usually requires a suspicion of this rare genitourinary syndrome.
We present ultrasonography and MR imaging findings of this rare anomaly in two cases.
Early recognition of this rare syndrome can lead to an immediate, proper surgical intervention and is necessary to prevent complications and preserve future fertility. Ultrasound and MR imaging findings can collectively delineate uterine morphology, indicate the absence of ipsilateral kidney and show obstructed hemivagina. |
| doi_str_mv | 10.12659/PJR.899889 |
| format | article |
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We present ultrasonography and MR imaging findings of this rare anomaly in two cases.
Early recognition of this rare syndrome can lead to an immediate, proper surgical intervention and is necessary to prevent complications and preserve future fertility. Ultrasound and MR imaging findings can collectively delineate uterine morphology, indicate the absence of ipsilateral kidney and show obstructed hemivagina.</description><identifier>ISSN: 1733-134X</identifier><identifier>ISSN: 1899-0967</identifier><identifier>EISSN: 1899-0967</identifier><identifier>DOI: 10.12659/PJR.899889</identifier><identifier>PMID: 28469738</identifier><language>eng</language><publisher>Poland: International Scientific Literature, Inc</publisher><subject>Case Report</subject><ispartof>Polish journal of radiology, 2017, Vol.82, p.216-219</ispartof><rights>Pol J Radiol, 2017 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c348t-590939e5e3026f701df7a0388c0d879fbc35895e8a14e6043eab5c9e100ecaed3</citedby><cites>FETCH-LOGICAL-c348t-590939e5e3026f701df7a0388c0d879fbc35895e8a14e6043eab5c9e100ecaed3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402867/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402867/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,4024,27923,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28469738$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yilmaz, Sukriye</creatorcontrib><creatorcontrib>Yildiz, Adalet Elcin</creatorcontrib><creatorcontrib>Fitoz, Suat</creatorcontrib><title>Herlyn-Werner-Wunderlich Syndrome: Sonographic and Magnetic Resonance (MR) Imaging Findings of This Rare Urogenital Anomaly</title><title>Polish journal of radiology</title><addtitle>Pol J Radiol</addtitle><description>Herlyn-Werner-Wunderlich syndrome is a rare congenital urogenital anomaly characterised by uterus didelphys with blind hemivagina and ipsilateral renal agenesis. Children usually have progressive pelvic pain after menarche, palpable mass due to hemihaemato(metro)colpos or pelvic inflammatory disease. The diagnosis usually requires a suspicion of this rare genitourinary syndrome.
We present ultrasonography and MR imaging findings of this rare anomaly in two cases.
Early recognition of this rare syndrome can lead to an immediate, proper surgical intervention and is necessary to prevent complications and preserve future fertility. Ultrasound and MR imaging findings can collectively delineate uterine morphology, indicate the absence of ipsilateral kidney and show obstructed hemivagina.</description><subject>Case Report</subject><issn>1733-134X</issn><issn>1899-0967</issn><issn>1899-0967</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNpVUU1LAzEQDaLYUnvyLjkqsjVp9iPxIJRibaVF6Qf1tqTZ2W1kNynZVij-eYPVonN5b77ewDyELinp0G4cibvX52mHC8G5OEFN6llARJycep4wFlAWvjVQu67fiY-YsjgMz1Gjy8NYJIw30ecQXLk3wRKcARcsdybzBa3WeLY3mbMV3OOZNbZwcrPWCkuT4YksDGx9MoXaGmkU4OvJ9AaPKlloU-CBNpnHGtscz9e6xlPpAC-cLcDorSxxz9hKlvsLdJbLsob2D7bQYvA47w-D8cvTqN8bB4qFfBtEgggmIAJGunGeEJrliSSMc0Uynoh8pVjERQRc0hBiEjKQq0gJoISAkpCxFno46G52qwoyBWbrZJlunK6k26dW6vR_x-h1WtiPNApJl8eJF7g9CChn69pBftylJP22IfU2pAcb_PTV33PH2d-nsy9DlIVW</recordid><startdate>2017</startdate><enddate>2017</enddate><creator>Yilmaz, Sukriye</creator><creator>Yildiz, Adalet Elcin</creator><creator>Fitoz, Suat</creator><general>International Scientific Literature, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>2017</creationdate><title>Herlyn-Werner-Wunderlich Syndrome: Sonographic and Magnetic Resonance (MR) Imaging Findings of This Rare Urogenital Anomaly</title><author>Yilmaz, Sukriye ; Yildiz, Adalet Elcin ; Fitoz, Suat</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c348t-590939e5e3026f701df7a0388c0d879fbc35895e8a14e6043eab5c9e100ecaed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Case Report</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yilmaz, Sukriye</creatorcontrib><creatorcontrib>Yildiz, Adalet Elcin</creatorcontrib><creatorcontrib>Fitoz, Suat</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Polish journal of radiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yilmaz, Sukriye</au><au>Yildiz, Adalet Elcin</au><au>Fitoz, Suat</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Herlyn-Werner-Wunderlich Syndrome: Sonographic and Magnetic Resonance (MR) Imaging Findings of This Rare Urogenital Anomaly</atitle><jtitle>Polish journal of radiology</jtitle><addtitle>Pol J Radiol</addtitle><date>2017</date><risdate>2017</risdate><volume>82</volume><spage>216</spage><epage>219</epage><pages>216-219</pages><issn>1733-134X</issn><issn>1899-0967</issn><eissn>1899-0967</eissn><abstract>Herlyn-Werner-Wunderlich syndrome is a rare congenital urogenital anomaly characterised by uterus didelphys with blind hemivagina and ipsilateral renal agenesis. Children usually have progressive pelvic pain after menarche, palpable mass due to hemihaemato(metro)colpos or pelvic inflammatory disease. The diagnosis usually requires a suspicion of this rare genitourinary syndrome.
We present ultrasonography and MR imaging findings of this rare anomaly in two cases.
Early recognition of this rare syndrome can lead to an immediate, proper surgical intervention and is necessary to prevent complications and preserve future fertility. Ultrasound and MR imaging findings can collectively delineate uterine morphology, indicate the absence of ipsilateral kidney and show obstructed hemivagina.</abstract><cop>Poland</cop><pub>International Scientific Literature, Inc</pub><pmid>28469738</pmid><doi>10.12659/PJR.899889</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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| ispartof | Polish journal of radiology, 2017, Vol.82, p.216-219 |
| issn | 1733-134X 1899-0967 1899-0967 |
| language | eng |
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| source | Open Access: PubMed Central |
| subjects | Case Report |
| title | Herlyn-Werner-Wunderlich Syndrome: Sonographic and Magnetic Resonance (MR) Imaging Findings of This Rare Urogenital Anomaly |
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