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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Fetal axillary cystic hygroma detected by prenatal ultrasonography: a case report.</title><author><name sortKey="Song, Tae Bok" sort="Song, Tae Bok" uniqKey="Song T" first="Tae-Bok" last="Song">Tae-Bok Song</name></author><author><name sortKey="Kim, Cheol Hong" sort="Kim, Cheol Hong" uniqKey="Kim C" first="Cheol-Hong" last="Kim">Cheol-Hong Kim</name></author><author><name sortKey="Kim, Seok Mo" sort="Kim, Seok Mo" uniqKey="Kim S" first="Seok-Mo" last="Kim">Seok-Mo Kim</name></author><author><name sortKey="Kim, Yoon Ha" sort="Kim, Yoon Ha" uniqKey="Kim Y" first="Yoon-Ha" last="Kim">Yoon-Ha Kim</name></author><author><name sortKey="Byun, Ji Soo" sort="Byun, Ji Soo" uniqKey="Byun J" first="Ji-Soo" last="Byun">Ji-Soo Byun</name></author><author><name sortKey="Kim, Eun Kyung" sort="Kim, Eun Kyung" uniqKey="Kim E" first="Eun-Kyung" last="Kim">Eun-Kyung Kim</name></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">12068147</idno><idno type="pmc">3054879</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054879</idno><idno type="RBID">PMC:3054879</idno><date when="2002">2002</date><idno type="wicri:Area/Pmc/Corpus">001D12</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001D12</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Fetal axillary cystic hygroma detected by prenatal ultrasonography: a case report.</title><author><name sortKey="Song, Tae Bok" sort="Song, Tae Bok" uniqKey="Song T" first="Tae-Bok" last="Song">Tae-Bok Song</name></author><author><name sortKey="Kim, Cheol Hong" sort="Kim, Cheol Hong" uniqKey="Kim C" first="Cheol-Hong" last="Kim">Cheol-Hong Kim</name></author><author><name sortKey="Kim, Seok Mo" sort="Kim, Seok Mo" uniqKey="Kim S" first="Seok-Mo" last="Kim">Seok-Mo Kim</name></author><author><name sortKey="Kim, Yoon Ha" sort="Kim, Yoon Ha" uniqKey="Kim Y" first="Yoon-Ha" last="Kim">Yoon-Ha Kim</name></author><author><name sortKey="Byun, Ji Soo" sort="Byun, Ji Soo" uniqKey="Byun J" first="Ji-Soo" last="Byun">Ji-Soo Byun</name></author><author><name sortKey="Kim, Eun Kyung" sort="Kim, Eun Kyung" uniqKey="Kim E" first="Eun-Kyung" last="Kim">Eun-Kyung Kim</name></author></analytic><series><title level="j">Journal of Korean Medical Science</title><idno type="ISSN">1011-8934</idno><idno type="eISSN">1598-6357</idno><imprint><date when="2002">2002</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Fetal cystic hygroma is a rare developmental congenital anomaly of the lymphatic system, characterized by the formation of a multilocular, variable sized cystic mass. Most of cystic hygromas are found in the neck and other rare locations include axilla, mediastinum, and limbs. There are many papers about cystic hygroma colli, but there are only a few papers about fetal axillary cystic hygroma and no domestic papers. We present a case of fetal axillary cystic hygroma diagnosed antenatally followed by full-term delivery in a 30-yr-old woman. Operation was performed on the 8th day after birth and the mass was excised and confirmed as cystic hygroma.</p></div></front></TEI><pmc article-type="review-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">J Korean Med Sci</journal-id><journal-id journal-id-type="pmc">jkms</journal-id><journal-title>Journal of Korean Medical Science</journal-title><issn pub-type="ppub">1011-8934</issn><issn pub-type="epub">1598-6357</issn><publisher><publisher-name>Korean Academy of Medical Sciences</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">12068147</article-id><article-id pub-id-type="pmc">3054879</article-id><article-id pub-id-type="pii">200206400</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title>Fetal axillary cystic hygroma detected by prenatal ultrasonography: a case report.</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Song</surname><given-names>Tae-Bok</given-names></name><email>tbsong@chonnam.chonnam.ac.kr</email></contrib><contrib contrib-type="author"><name><surname>Kim</surname><given-names>Cheol-Hong</given-names></name></contrib><contrib contrib-type="author"><name><surname>Kim</surname><given-names>Seok-Mo</given-names></name></contrib><contrib contrib-type="author"><name><surname>Kim</surname><given-names>Yoon-Ha</given-names></name></contrib><contrib contrib-type="author"><name><surname>Byun</surname><given-names>Ji-Soo</given-names></name></contrib><contrib contrib-type="author"><name><surname>Kim</surname><given-names>Eun-Kyung</given-names></name></contrib></contrib-group><aff>Department of Obstetrics and Gynecology, Chonnam National University Medical School and Research Institute of Medical Sciences, Chonnam National University, Korea.</aff><pub-date pub-type="ppub"><month>6</month><year>2002</year></pub-date><volume>17</volume><issue>3</issue><fpage>400</fpage><lpage>402</lpage><abstract><p>Fetal cystic hygroma is a rare developmental congenital anomaly of the lymphatic system, characterized by the formation of a multilocular, variable sized cystic mass. Most of cystic hygromas are found in the neck and other rare locations include axilla, mediastinum, and limbs. There are many papers about cystic hygroma colli, but there are only a few papers about fetal axillary cystic hygroma and no domestic papers. We present a case of fetal axillary cystic hygroma diagnosed antenatally followed by full-term delivery in a 30-yr-old woman. Operation was performed on the 8th day after birth and the mass was excised and confirmed as cystic hygroma.</p></abstract></article-meta></front></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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