Antenatally diagnosed cloacal exstrophy variant with intravesical phallus in a twin pregnancy
We report a rare case of covered cloacal exstrophy variant with a hemiphallus trapped within partially closed bladder halves. The persistence of the cloacal membrane until at least 18 weeks’ gestation, confirmed by antenatal ultrasound scanning, is discordant with existing theories of embryogenesis...
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Veröffentlicht in: | Urology (Ridgewood, N.J.) N.J.), 2001-06, Vol.57 (6), p.1178-1178 |
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creator | Lakshmanan, Yegappan Bellin, Paula B Gilroy, Anne M Fung, Leo C.T |
description | We report a rare case of covered cloacal exstrophy variant with a hemiphallus trapped within partially closed bladder halves. The persistence of the cloacal membrane until at least 18 weeks’ gestation, confirmed by antenatal ultrasound scanning, is discordant with existing theories of embryogenesis of cloacal exstrophy. The clinical presentation highlights the need for careful assessment, before and during surgery, to obtain a complete understanding of the anatomic defect before gender assignment and appropriate reconstructive efforts. A multispecialty approach and antenatal counseling are important, especially when only one fetus of twins has major birth defects. |
doi_str_mv | 10.1016/S0090-4295(01)01082-2 |
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The persistence of the cloacal membrane until at least 18 weeks’ gestation, confirmed by antenatal ultrasound scanning, is discordant with existing theories of embryogenesis of cloacal exstrophy. The clinical presentation highlights the need for careful assessment, before and during surgery, to obtain a complete understanding of the anatomic defect before gender assignment and appropriate reconstructive efforts. 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The persistence of the cloacal membrane until at least 18 weeks’ gestation, confirmed by antenatal ultrasound scanning, is discordant with existing theories of embryogenesis of cloacal exstrophy. The clinical presentation highlights the need for careful assessment, before and during surgery, to obtain a complete understanding of the anatomic defect before gender assignment and appropriate reconstructive efforts. A multispecialty approach and antenatal counseling are important, especially when only one fetus of twins has major birth defects.</description><subject>Abnormalities, Multiple - diagnostic imaging</subject><subject>Abnormalities, Multiple - surgery</subject><subject>Anus, Imperforate - surgery</subject><subject>Bladder Exstrophy - diagnostic imaging</subject><subject>Bladder Exstrophy - embryology</subject><subject>Bladder Exstrophy - surgery</subject><subject>Diseases in Twins - embryology</subject><subject>Fatal Outcome</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Male</subject><subject>Penis - abnormalities</subject><subject>Penis - diagnostic imaging</subject><subject>Penis - surgery</subject><subject>Ultrasonography</subject><issn>0090-4295</issn><issn>1527-9995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtLxDAQx4Mouj4-gtKT6KE66SvNSUR8geBBPUqYptPdSDetSXZ1v73dB3r0NDD8_vP4MXbM4YIDLy5fACTEWSLzM-DnwKFM4mSLjXieiFhKmW-z0S-yx_a9_wCAoijELtvjPBUiTeWIvV_bQBYDtu0iqg2ObeepjnTbocY2om8fXNdPFtEcnUEboi8TJpGxweGcvFky_WQIz_zQjDAKX0PpHY0tWr04ZDsNtp6ONvWAvd3dvt48xE_P948310-xTkQR4gYbrCqNvMzKrMpzBC0b0JkWZSXLiiRveFXLVDbD2ZTXiFkicgEohSglpekBO13P7V33OSMf1NR4TW2LlrqZVyLJMpBFMoD5GtSu895Ro3pnpugWioNaelUrr2opTQFXK69qmTvZLJhVU6r_UhuRA3C1Bmh4c27IKa8NWU21caSDqjvzz4ofteyJxQ</recordid><startdate>200106</startdate><enddate>200106</enddate><creator>Lakshmanan, Yegappan</creator><creator>Bellin, Paula B</creator><creator>Gilroy, Anne M</creator><creator>Fung, Leo C.T</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200106</creationdate><title>Antenatally diagnosed cloacal exstrophy variant with intravesical phallus in a twin pregnancy</title><author>Lakshmanan, Yegappan ; Bellin, Paula B ; Gilroy, Anne M ; Fung, Leo C.T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c276t-fafabbca18484b55a0c9f0c4c78b98be91f1bd939f377e5daa427570a97789e33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Abnormalities, Multiple - diagnostic imaging</topic><topic>Abnormalities, Multiple - surgery</topic><topic>Anus, Imperforate - surgery</topic><topic>Bladder Exstrophy - diagnostic imaging</topic><topic>Bladder Exstrophy - embryology</topic><topic>Bladder Exstrophy - surgery</topic><topic>Diseases in Twins - embryology</topic><topic>Fatal Outcome</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Male</topic><topic>Penis - abnormalities</topic><topic>Penis - diagnostic imaging</topic><topic>Penis - surgery</topic><topic>Ultrasonography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lakshmanan, Yegappan</creatorcontrib><creatorcontrib>Bellin, Paula B</creatorcontrib><creatorcontrib>Gilroy, Anne M</creatorcontrib><creatorcontrib>Fung, Leo C.T</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Urology (Ridgewood, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lakshmanan, Yegappan</au><au>Bellin, Paula B</au><au>Gilroy, Anne M</au><au>Fung, Leo C.T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antenatally diagnosed cloacal exstrophy variant with intravesical phallus in a twin pregnancy</atitle><jtitle>Urology (Ridgewood, N.J.)</jtitle><addtitle>Urology</addtitle><date>2001-06</date><risdate>2001</risdate><volume>57</volume><issue>6</issue><spage>1178</spage><epage>1178</epage><pages>1178-1178</pages><issn>0090-4295</issn><eissn>1527-9995</eissn><abstract>We report a rare case of covered cloacal exstrophy variant with a hemiphallus trapped within partially closed bladder halves. The persistence of the cloacal membrane until at least 18 weeks’ gestation, confirmed by antenatal ultrasound scanning, is discordant with existing theories of embryogenesis of cloacal exstrophy. The clinical presentation highlights the need for careful assessment, before and during surgery, to obtain a complete understanding of the anatomic defect before gender assignment and appropriate reconstructive efforts. A multispecialty approach and antenatal counseling are important, especially when only one fetus of twins has major birth defects.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>11377339</pmid><doi>10.1016/S0090-4295(01)01082-2</doi><tpages>1</tpages></addata></record> |
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subjects | Abnormalities, Multiple - diagnostic imaging Abnormalities, Multiple - surgery Anus, Imperforate - surgery Bladder Exstrophy - diagnostic imaging Bladder Exstrophy - embryology Bladder Exstrophy - surgery Diseases in Twins - embryology Fatal Outcome Humans Infant, Newborn Male Penis - abnormalities Penis - diagnostic imaging Penis - surgery Ultrasonography |
title | Antenatally diagnosed cloacal exstrophy variant with intravesical phallus in a twin pregnancy |
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