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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Chylous ascites, intestinal lymphangiectasia and the 'yellow-nail' syndrome.</title><author><name sortKey="Duhra, P M" sort="Duhra, P M" uniqKey="Duhra P" first="P M" last="Duhra">P M Duhra</name></author><author><name sortKey="Quigley, E M" sort="Quigley, E M" uniqKey="Quigley E" first="E M" last="Quigley">E M Quigley</name></author><author><name sortKey="Marsh, M N" sort="Marsh, M N" uniqKey="Marsh M" first="M N" last="Marsh">M N Marsh</name></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">4065700</idno><idno type="pmc">1432907</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1432907</idno><idno type="RBID">PMC:1432907</idno><date when="1985">1985</date><idno type="wicri:Area/Pmc/Corpus">001777</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001777</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Chylous ascites, intestinal lymphangiectasia and the 'yellow-nail' syndrome.</title><author><name sortKey="Duhra, P M" sort="Duhra, P M" uniqKey="Duhra P" first="P M" last="Duhra">P M Duhra</name></author><author><name sortKey="Quigley, E M" sort="Quigley, E M" uniqKey="Quigley E" first="E M" last="Quigley">E M Quigley</name></author><author><name sortKey="Marsh, M N" sort="Marsh, M N" uniqKey="Marsh M" first="M N" last="Marsh">M N Marsh</name></author></analytic><series><title level="j">Gut</title><idno type="ISSN">0017-5749</idno><idno type="eISSN">1458-3288</idno><imprint><date when="1985">1985</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>In 1964 Samman and White described 13 patients with lymphoedema of the lower extremities associated with an unusual dystrophy of the finger and toe nails: this they termed the 'yellow-nail' syndrome. Affected nails were thickened, excessively curved along both axes, very slow growing and of yellowish-grey hue; cuticle and lunula were usually absent and onycholysis was frequently evident. Lower limb lymphangiography in most individuals revealed hypoplasia, or aplasia of the lymphatics, similar to that occurring in primary lymphoedema: other patients also developed pleural effusions of high protein content or ascites suggestive of a more generalised disorder of the lymphatic system. Here we describe a patient in whom the classical 'yellow-nail' syndrome was associated with intestinal and chylous ascites.</p><sec sec-type="scanned-figures"><title>Images</title><fig id="F1"><label>Fig. 1</label><graphic xlink:href="gut00384-0127-a" xlink:role="1267"></graphic></fig><fig id="F2"><label>Fig. 2</label><graphic xlink:href="gut00384-0128-a" xlink:role="1268"></graphic></fig><fig id="F3"><label>Fig. 3</label><graphic xlink:href="gut00384-0129-a" xlink:role="1269"></graphic></fig></sec></div></front></TEI><pmc article-type="research-article"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Gut</journal-id><journal-title>Gut</journal-title><issn pub-type="ppub">0017-5749</issn><issn pub-type="epub">1458-3288</issn></journal-meta><article-meta><article-id pub-id-type="pmid">4065700</article-id><article-id pub-id-type="pmc">1432907</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title>Chylous ascites, intestinal lymphangiectasia and the 'yellow-nail' syndrome.</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Duhra</surname><given-names>P M</given-names></name></contrib><contrib contrib-type="author"><name><surname>Quigley</surname><given-names>E M</given-names></name></contrib><contrib contrib-type="author"><name><surname>Marsh</surname><given-names>M N</given-names></name></contrib></contrib-group><pub-date pub-type="ppub"><month>11</month><year>1985</year></pub-date><volume>26</volume><issue>11</issue><fpage>1266</fpage><lpage>1269</lpage><abstract><p>In 1964 Samman and White described 13 patients with lymphoedema of the lower extremities associated with an unusual dystrophy of the finger and toe nails: this they termed the 'yellow-nail' syndrome. Affected nails were thickened, excessively curved along both axes, very slow growing and of yellowish-grey hue; cuticle and lunula were usually absent and onycholysis was frequently evident. Lower limb lymphangiography in most individuals revealed hypoplasia, or aplasia of the lymphatics, similar to that occurring in primary lymphoedema: other patients also developed pleural effusions of high protein content or ascites suggestive of a more generalised disorder of the lymphatic system. Here we describe a patient in whom the classical 'yellow-nail' syndrome was associated with intestinal and chylous ascites.</p><sec sec-type="scanned-figures"><title>Images</title><fig id="F1"><label>Fig. 1</label><graphic xlink:href="gut00384-0127-a" xlink:role="1267"></graphic></fig><fig id="F2"><label>Fig. 2</label><graphic xlink:href="gut00384-0128-a" xlink:role="1268"></graphic></fig><fig id="F3"><label>Fig. 3</label><graphic xlink:href="gut00384-0129-a" xlink:role="1269"></graphic></fig></sec></abstract></article-meta></front></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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