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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Inguinal lymphadenopathy as the initial presentation of sarcoidosis</title>
<author><name sortKey="George, Jim" sort="George, Jim" uniqKey="George J" first="Jim" last="George">Jim George</name>
</author>
<author><name sortKey="Graves, Reese" sort="Graves, Reese" uniqKey="Graves R" first="Reese" last="Graves">Reese Graves</name>
</author>
<author><name sortKey="Meador, Robert" sort="Meador, Robert" uniqKey="Meador R" first="Robert" last="Meador">Robert Meador</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PMC</idno>
<idno type="pmid">23543976</idno>
<idno type="pmc">3603735</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3603735</idno>
<idno type="RBID">PMC:3603735</idno>
<date when="2013">2013</date>
<idno type="wicri:Area/Pmc/Corpus">002082</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">002082</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Inguinal lymphadenopathy as the initial presentation of sarcoidosis</title>
<author><name sortKey="George, Jim" sort="George, Jim" uniqKey="George J" first="Jim" last="George">Jim George</name>
</author>
<author><name sortKey="Graves, Reese" sort="Graves, Reese" uniqKey="Graves R" first="Reese" last="Graves">Reese Graves</name>
</author>
<author><name sortKey="Meador, Robert" sort="Meador, Robert" uniqKey="Meador R" first="Robert" last="Meador">Robert Meador</name>
</author>
</analytic>
<series><title level="j">Proceedings (Baylor University. Medical Center)</title>
<idno type="ISSN">0899-8280</idno>
<imprint><date when="2013">2013</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass></textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en"><p>Sarcoidosis is a multisystem disease of unknown etiology characterized by granuloma formation. Despite pulmonary involvement in most patients, sarcoidosis can have a varied presentation. Lymph node involvement is rarely found in isolation. Even rarer are cases of sarcoidosis presenting with peripheral edema. We describe a case of sarcoidosis presenting with isolated unilateral peripheral edema.</p>
</div>
</front>
</TEI>
<pmc article-type="case-report"><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">Proc (Bayl Univ Med Cent)</journal-id>
<journal-id journal-id-type="iso-abbrev">Proc (Bayl Univ Med Cent)</journal-id>
<journal-id journal-id-type="publisher-id">bumc</journal-id>
<journal-title-group><journal-title>Proceedings (Baylor University. Medical Center)</journal-title>
</journal-title-group>
<issn pub-type="ppub">0899-8280</issn>
<publisher><publisher-name>Baylor Health Care System</publisher-name>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">23543976</article-id>
<article-id pub-id-type="pmc">3603735</article-id>
<article-id pub-id-type="publisher-id">bumc0026-0161</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Case Studies</subject>
</subj-group>
</article-categories>
<title-group><article-title>Inguinal lymphadenopathy as the initial presentation of sarcoidosis</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" corresp="yes"><name><surname>George</surname>
<given-names>Jim</given-names>
</name>
<degrees>MD</degrees>
</contrib>
<contrib contrib-type="author"><name><surname>Graves</surname>
<given-names>Reese</given-names>
</name>
<degrees>MD</degrees>
</contrib>
<contrib contrib-type="author"><name><surname>Meador</surname>
<given-names>Robert</given-names>
<suffix>Jr.</suffix>
</name>
<degrees>MD</degrees>
</contrib>
</contrib-group>
<aff>From the Department of Family Medicine (George, Graves), and the Division of Rheumatology, Department of Internal Medicine (Meador), Baylor Medical Center at Garland, Garland, Texas.</aff>
<author-notes><corresp><bold>Corresponding author:</bold>
Corresponding author: Jim George, MD, 1009 East Grubb Drive, Mesquite, TX 75149 (e-mail: <email>Jim.george.dallas@gmail.com</email>
).</corresp>
</author-notes>
<pub-date pub-type="ppub"><month>4</month>
<year>2013</year>
</pub-date>
<volume>26</volume>
<issue>2</issue>
<fpage>161</fpage>
<lpage>162</lpage>
<ext-link ext-link-type="uri" xlink:href="http://www.BaylorHealth.com/Proceedings">http://www.BaylorHealth.com/Proceedings</ext-link>
<permissions><copyright-statement>Copyright © 2013, Baylor University Medical Center</copyright-statement>
<copyright-year>2013</copyright-year>
</permissions>
<abstract><p>Sarcoidosis is a multisystem disease of unknown etiology characterized by granuloma formation. Despite pulmonary involvement in most patients, sarcoidosis can have a varied presentation. Lymph node involvement is rarely found in isolation. Even rarer are cases of sarcoidosis presenting with peripheral edema. We describe a case of sarcoidosis presenting with isolated unilateral peripheral edema.</p>
</abstract>
</article-meta>
</front>
</pmc>
</record>
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