Prenatal diagnosis and management of massive bilateral axillary cystic lymphangioma
Identifieur interne : 001C17 ( Istex/Corpus ); précédent : 001C16; suivant : 001C18Prenatal diagnosis and management of massive bilateral axillary cystic lymphangioma
Auteurs : M. Cathleen Mccoy ; Jeffrey A. Kuller ; Nancy C. Chescheir ; Carol C. Coulson ; Vern L. Katz ; Don K. NakayamaSource :
- Obstetrics & Gynecology [ 0029-7844 ] ; 1995.
Abstract
Background: Fetal lymphangiomas can occur in many different anatomic locations, including the most commonly seen nuchal cystic hygroma.Case: A fetus at 18 weeks' gestation was found to have a massive right axillary hygroma. The fetal karyotype was normal. Serial ultrasound examinations indicated progressive enlargement, but no hydrops. At 32 weeks' gestation, a left axillary hygroma was also diagnosed. The patient underwent cesarean delivery.Conclusion: Prenatal diagnosis of nuchal cystic hygromas has a high association with karyotypic abnormalities, hydrops, and fetal demise; however, this association may not apply to cystic lymphangiomas at other locations.
Url:
DOI: 10.1016/0029-7844(94)00312-2
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ISTEX:3D85BDD3B5E38607A381C7CA092A9CC92E096051Le document en format XML
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Kuller</name><affiliation><mods:affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</mods:affiliation></affiliation></author><author><name sortKey="Chescheir, Nancy C" sort="Chescheir, Nancy C" uniqKey="Chescheir N" first="Nancy C." last="Chescheir">Nancy C. Chescheir</name><affiliation><mods:affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</mods:affiliation></affiliation></author><author><name sortKey="Coulson, Carol C" sort="Coulson, Carol C" uniqKey="Coulson C" first="Carol C." last="Coulson">Carol C. Coulson</name><affiliation><mods:affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</mods:affiliation></affiliation></author><author><name sortKey="Katz, Vern L" sort="Katz, Vern L" uniqKey="Katz V" first="Vern L." last="Katz">Vern L. Katz</name><affiliation><mods:affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</mods:affiliation></affiliation></author><author><name sortKey="Nakayama, Don K" sort="Nakayama, Don K" uniqKey="Nakayama D" first="Don K." last="Nakayama">Don K. 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Cathleen" last="Mccoy">M. Cathleen Mccoy</name><affiliation><mods:affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</mods:affiliation></affiliation></author><author><name sortKey="Kuller, Jeffrey A" sort="Kuller, Jeffrey A" uniqKey="Kuller J" first="Jeffrey A." last="Kuller">Jeffrey A. Kuller</name><affiliation><mods:affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</mods:affiliation></affiliation></author><author><name sortKey="Chescheir, Nancy C" sort="Chescheir, Nancy C" uniqKey="Chescheir N" first="Nancy C." last="Chescheir">Nancy C. Chescheir</name><affiliation><mods:affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</mods:affiliation></affiliation></author><author><name sortKey="Coulson, Carol C" sort="Coulson, Carol C" uniqKey="Coulson C" first="Carol C." last="Coulson">Carol C. Coulson</name><affiliation><mods:affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</mods:affiliation></affiliation></author><author><name sortKey="Katz, Vern L" sort="Katz, Vern L" uniqKey="Katz V" first="Vern L." last="Katz">Vern L. Katz</name><affiliation><mods:affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</mods:affiliation></affiliation></author><author><name sortKey="Nakayama, Don K" sort="Nakayama, Don K" uniqKey="Nakayama D" first="Don K." last="Nakayama">Don K. Nakayama</name><affiliation><mods:affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Obstetrics & Gynecology</title><title level="j" type="abbrev">ONG</title><idno type="ISSN">0029-7844</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1995">1995</date><biblScope unit="volume">85</biblScope><biblScope unit="issue">5</biblScope><biblScope unit="supplement">P2</biblScope><biblScope unit="page" from="853">853</biblScope><biblScope unit="page" to="856">856</biblScope></imprint><idno type="ISSN">0029-7844</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0029-7844</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract">Background: Fetal lymphangiomas can occur in many different anatomic locations, including the most commonly seen nuchal cystic hygroma.Case: A fetus at 18 weeks' gestation was found to have a massive right axillary hygroma. The fetal karyotype was normal. Serial ultrasound examinations indicated progressive enlargement, but no hydrops. At 32 weeks' gestation, a left axillary hygroma was also diagnosed. The patient underwent cesarean delivery.Conclusion: Prenatal diagnosis of nuchal cystic hygromas has a high association with karyotypic abnormalities, hydrops, and fetal demise; however, this association may not apply to cystic lymphangiomas at other locations.</div></front></TEI><istex><corpusName>elsevier</corpusName><keywords><teeft><json:string>lymphangioma</json:string><json:string>axillary</json:string><json:string>hygroma</json:string><json:string>cystic</json:string><json:string>fetal</json:string><json:string>prenatal</json:string><json:string>ultrasound</json:string><json:string>gestation</json:string><json:string>cystic hygroma</json:string><json:string>nuchal</json:string><json:string>karyotype</json:string><json:string>lymphatic</json:string><json:string>obstetrics</json:string><json:string>prenatal diagnosis</json:string><json:string>hygromas</json:string><json:string>prenatally</json:string><json:string>gynecology</json:string><json:string>axilla</json:string><json:string>hydrops</json:string><json:string>mccoy</json:string><json:string>neonate</json:string><json:string>cystic lymphangiomas</json:string><json:string>obstet</json:string><json:string>cystic lymphangioma</json:string><json:string>axillary mass</json:string><json:string>ultrasound examination</json:string><json:string>cathleen mccoy</json:string><json:string>cesarean delivery</json:string><json:string>anatomic locations</json:string><json:string>chapel hill</json:string><json:string>surgical excision</json:string><json:string>chest wall</json:string><json:string>postoperative course</json:string><json:string>shoulder dystocia</json:string><json:string>american college</json:string><json:string>axillary lymphangiomas</json:string><json:string>prenat diagn</json:string></teeft></keywords><author><json:item><name>M. Cathleen McCoy MD</name><affiliations><json:string>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</json:string></affiliations></json:item><json:item><name>Jeffrey A. Kuller MD</name><affiliations><json:string>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</json:string></affiliations></json:item><json:item><name>Nancy C. Chescheir MD</name><affiliations><json:string>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</json:string></affiliations></json:item><json:item><name>Carol C. Coulson MD</name><affiliations><json:string>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</json:string></affiliations></json:item><json:item><name>Vern L. Katz MD</name><affiliations><json:string>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</json:string></affiliations></json:item><json:item><name>Don K. Nakayama MD</name><affiliations><json:string>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</json:string></affiliations></json:item></author><articleId><json:string>94003122</json:string></articleId><language><json:string>eng</json:string></language><originalGenre><json:string>Full-length article</json:string></originalGenre><abstract>Background: Fetal lymphangiomas can occur in many different anatomic locations, including the most commonly seen nuchal cystic hygroma.Case: A fetus at 18 weeks' gestation was found to have a massive right axillary hygroma. The fetal karyotype was normal. Serial ultrasound examinations indicated progressive enlargement, but no hydrops. At 32 weeks' gestation, a left axillary hygroma was also diagnosed. The patient underwent cesarean delivery.Conclusion: Prenatal diagnosis of nuchal cystic hygromas has a high association with karyotypic abnormalities, hydrops, and fetal demise; however, this association may not apply to cystic lymphangiomas at other locations.</abstract><qualityIndicators><score>3.641</score><pdfVersion>1.4</pdfVersion><pdfPageSize>576 x 792 pts</pdfPageSize><refBibsNative>true</refBibsNative><keywordCount>0</keywordCount><abstractCharCount>667</abstractCharCount><pdfWordCount>2037</pdfWordCount><pdfCharCount>12926</pdfCharCount><pdfPageCount>4</pdfPageCount><abstractWordCount>92</abstractWordCount></qualityIndicators><title>Prenatal diagnosis and management of massive bilateral axillary cystic lymphangioma</title><pii><json:string>0029-7844(94)00312-2</json:string></pii><genre><json:string>research-article</json:string></genre><serie><title>Human malformations and related anomalies</title><language><json:string>unknown</json:string></language><volume>vol. 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Cathleen</forename><surname>McCoy</surname></persName><roleName type="degree">MD</roleName><note type="biography">Address reprint requests to: M. Cathleen McCoy, MD, University of North Carolina School of Medicine, Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, CB# 7570, 214 MacNider Building, Chapel Hill, NC 27599-7570</note><affiliation>Address reprint requests to: M. Cathleen McCoy, MD, University of North Carolina School of Medicine, Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, CB# 7570, 214 MacNider Building, Chapel Hill, NC 27599-7570</affiliation><affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</affiliation></author><author xml:id="author-0001"><persName><forename type="first">Jeffrey A.</forename><surname>Kuller</surname></persName><roleName type="degree">MD</roleName><affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</affiliation></author><author xml:id="author-0002"><persName><forename type="first">Nancy C.</forename><surname>Chescheir</surname></persName><roleName type="degree">MD</roleName><affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</affiliation></author><author xml:id="author-0003"><persName><forename type="first">Carol C.</forename><surname>Coulson</surname></persName><roleName type="degree">MD</roleName><affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</affiliation></author><author xml:id="author-0004"><persName><forename type="first">Vern L.</forename><surname>Katz</surname></persName><roleName type="degree">MD</roleName><affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</affiliation></author><author xml:id="author-0005"><persName><forename type="first">Don K.</forename><surname>Nakayama</surname></persName><roleName type="degree">MD</roleName><affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</affiliation></author><idno type="istex">3D85BDD3B5E38607A381C7CA092A9CC92E096051</idno><idno type="DOI">10.1016/0029-7844(94)00312-2</idno><idno type="PII">0029-7844(94)00312-2</idno><idno type="ArticleID">94003122</idno></analytic><monogr><title level="j">Obstetrics & Gynecology</title><title level="j" type="abbrev">ONG</title><idno type="pISSN">0029-7844</idno><idno type="PII">S0029-7844(99)X0124-4</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1995"></date><biblScope unit="volume">85</biblScope><biblScope unit="issue">5</biblScope><biblScope unit="supplement">P2</biblScope><biblScope unit="page" from="853">853</biblScope><biblScope unit="page" to="856">856</biblScope></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>1995</date></creation><langUsage><language ident="en">en</language></langUsage><abstract><p>Background: Fetal lymphangiomas can occur in many different anatomic locations, including the most commonly seen nuchal cystic hygroma.Case: A fetus at 18 weeks' gestation was found to have a massive right axillary hygroma. The fetal karyotype was normal. Serial ultrasound examinations indicated progressive enlargement, but no hydrops. At 32 weeks' gestation, a left axillary hygroma was also diagnosed. The patient underwent cesarean delivery.Conclusion: Prenatal diagnosis of nuchal cystic hygromas has a high association with karyotypic abnormalities, hydrops, and fetal demise; however, this association may not apply to cystic lymphangiomas at other locations.</p></abstract></profileDesc><revisionDesc><change when="1994-08-01">Modified</change><change when="1995">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/3D85BDD3B5E38607A381C7CA092A9CC92E096051/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Elsevier doc found" wicri:toSee="Elsevier, no converted or simple article"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" </istex:xmlDeclaration><istex:docType PUBLIC="-//ES//DTD journal article DTD version 5.1.0//EN//XML" URI="art510.dtd" name="istex:docType"></istex:docType><istex:document><article version="5.1" xml:lang="en" docsubtype="fla"><item-info><jid>ONG</jid><aid>94003122</aid><ce:pii>0029-7844(94)00312-2</ce:pii><ce:doi>10.1016/0029-7844(94)00312-2</ce:doi><ce:copyright type="other" year="1995">The American College of Obstetricians and Gynecologists</ce:copyright></item-info><head><ce:title>Prenatal diagnosis and management of massive bilateral axillary cystic lymphangioma</ce:title><ce:author-group><ce:author><ce:given-name>M. Cathleen</ce:given-name><ce:surname>McCoy</ce:surname><ce:degrees>MD</ce:degrees><ce:cross-ref refid="cor1"><ce:sup>*</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>Jeffrey A.</ce:given-name><ce:surname>Kuller</ce:surname><ce:degrees>MD</ce:degrees></ce:author><ce:author><ce:given-name>Nancy C.</ce:given-name><ce:surname>Chescheir</ce:surname><ce:degrees>MD</ce:degrees></ce:author><ce:author><ce:given-name>Carol C.</ce:given-name><ce:surname>Coulson</ce:surname><ce:degrees>MD</ce:degrees></ce:author><ce:author><ce:given-name>Vern L.</ce:given-name><ce:surname>Katz</ce:surname><ce:degrees>MD</ce:degrees></ce:author><ce:author><ce:given-name>Don K.</ce:given-name><ce:surname>Nakayama</ce:surname><ce:degrees>MD</ce:degrees></ce:author><ce:affiliation id="aff1"><ce:label>a</ce:label><ce:textfn>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</ce:textfn></ce:affiliation><ce:affiliation id="aff2"><ce:label>b</ce:label><ce:textfn>Department of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</ce:textfn></ce:affiliation><ce:correspondence id="cor1"><ce:label>*</ce:label><ce:text>Address reprint requests to: <ce:italic>M. Cathleen McCoy, MD, University of North Carolina School of Medicine, Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, CB# 7570, 214 MacNider Building, Chapel Hill, NC 27599-7570</ce:italic></ce:text></ce:correspondence></ce:author-group><ce:date-received day="1" month="6" year="1994"></ce:date-received><ce:date-revised day="1" month="8" year="1994"></ce:date-revised><ce:date-accepted day="2" month="8" year="1994"></ce:date-accepted><ce:abstract id="ab1"><ce:abstract-sec><ce:simple-para id="SP0005"><ce:italic>Background</ce:italic>: Fetal lymphangiomas can occur in many different anatomic locations, including the most commonly seen nuchal cystic hygroma.</ce:simple-para><ce:simple-para id="SP0010"><ce:italic>Case</ce:italic>: A fetus at 18 weeks' gestation was found to have a massive right axillary hygroma. The fetal karyotype was normal. Serial ultrasound examinations indicated progressive enlargement, but no hydrops. At 32 weeks' gestation, a left axillary hygroma was also diagnosed. 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diagnosis and management of massive bilateral axillary cystic lymphangioma</title></titleInfo><name type="personal"><namePart type="given">M. Cathleen</namePart><namePart type="family">McCoy</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</affiliation><description>Address reprint requests to: M. Cathleen McCoy, MD, University of North Carolina School of Medicine, Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, CB# 7570, 214 MacNider Building, Chapel Hill, NC 27599-7570</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Jeffrey A.</namePart><namePart type="family">Kuller</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Nancy C.</namePart><namePart type="family">Chescheir</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Carol C.</namePart><namePart type="family">Coulson</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Vern L.</namePart><namePart type="family">Katz</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Don K.</namePart><namePart type="family">Nakayama</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="Full-length article"></genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1995</dateIssued><dateModified encoding="w3cdtf">1994-08-01</dateModified><copyrightDate encoding="w3cdtf">1995</copyrightDate></originInfo><language><languageTerm type="code" authority="iso639-2b">eng</languageTerm><languageTerm type="code" authority="rfc3066">en</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType></physicalDescription><abstract>Background: Fetal lymphangiomas can occur in many different anatomic locations, including the most commonly seen nuchal cystic hygroma.Case: A fetus at 18 weeks' gestation was found to have a massive right axillary hygroma. The fetal karyotype was normal. Serial ultrasound examinations indicated progressive enlargement, but no hydrops. At 32 weeks' gestation, a left axillary hygroma was also diagnosed. The patient underwent cesarean delivery.Conclusion: Prenatal diagnosis of nuchal cystic hygromas has a high association with karyotypic abnormalities, hydrops, and fetal demise; however, this association may not apply to cystic lymphangiomas at other locations.</abstract><relatedItem type="host"><titleInfo><title>Obstetrics & Gynecology</title></titleInfo><titleInfo type="abbreviated"><title>ONG</title></titleInfo><genre type="journal">journal</genre><originInfo><dateIssued encoding="w3cdtf">199505</dateIssued></originInfo><identifier type="ISSN">0029-7844</identifier><identifier type="PII">S0029-7844(99)X0124-4</identifier><part><date>199505</date><detail type="volume"><number>85</number><caption>vol.</caption></detail><detail type="issue"><number>5</number><caption>no.</caption></detail><detail type="supplement"><number>P2</number><caption>Suppl.</caption></detail><extent unit="issue pages"><start>806</start><end>908</end></extent><extent unit="pages"><start>853</start><end>856</end></extent></part></relatedItem><identifier type="istex">3D85BDD3B5E38607A381C7CA092A9CC92E096051</identifier><identifier type="DOI">10.1016/0029-7844(94)00312-2</identifier><identifier type="PII">0029-7844(94)00312-2</identifier><identifier type="ArticleID">94003122</identifier><accessCondition type="use and reproduction" contentType="copyright">©1995 The American College of Obstetricians and Gynecologists</accessCondition><recordInfo><recordContentSource>ELSEVIER</recordContentSource><recordOrigin>The American College of Obstetricians and Gynecologists, ©1995</recordOrigin></recordInfo></mods></metadata></istex></record>Pour manipuler ce document sous Unix (Dilib)
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