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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Klippel-Trenaunay Syndrome: a case report with brief review of literature</title><author><name sortKey="Zea, Mohammad Iqbal" sort="Zea, Mohammad Iqbal" uniqKey="Zea M" first="Mohammad Iqbal" last="Zea">Mohammad Iqbal Zea</name></author><author><name sortKey="Hanif, Mohammad" sort="Hanif, Mohammad" uniqKey="Hanif M" first="Mohammad" last="Hanif">Mohammad Hanif</name></author><author><name sortKey="Habib, Mohammad" sort="Habib, Mohammad" uniqKey="Habib M" first="Mohammad" last="Habib">Mohammad Habib</name></author><author><name sortKey="Ansari, Ahmed" sort="Ansari, Ahmed" uniqKey="Ansari A" first="Ahmed" last="Ansari">Ahmed Ansari</name></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">21886734</idno><idno type="pmc">3163347</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3163347</idno><idno type="RBID">PMC:3163347</idno><idno type="doi">10.3315/jdcr.2009.1038</idno><date when="2009">2009</date><idno type="wicri:Area/Pmc/Corpus">002064</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">002064</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Klippel-Trenaunay Syndrome: a case report with brief review of literature</title><author><name sortKey="Zea, Mohammad Iqbal" sort="Zea, Mohammad Iqbal" uniqKey="Zea M" first="Mohammad Iqbal" last="Zea">Mohammad Iqbal Zea</name></author><author><name sortKey="Hanif, Mohammad" sort="Hanif, Mohammad" uniqKey="Hanif M" first="Mohammad" last="Hanif">Mohammad Hanif</name></author><author><name sortKey="Habib, Mohammad" sort="Habib, Mohammad" uniqKey="Habib M" first="Mohammad" last="Habib">Mohammad Habib</name></author><author><name sortKey="Ansari, Ahmed" sort="Ansari, Ahmed" uniqKey="Ansari A" first="Ahmed" last="Ansari">Ahmed Ansari</name></author></analytic><series><title level="j">Journal of Dermatological Case Reports</title><idno type="eISSN">1898-7249</idno><imprint><date when="2009">2009</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><sec id="st1"><title>Background</title><p>Klippel-Tranuanay Syndrome is a rare sporadic disease characterized by clinical triad of capillary malformation; soft tissue and bony hypertrophy; and atypical varicosity. Although this syndrome was first described more than hundred years ago, exact incidence has not been estimated yet. Several theories have been postulated to describe its pathogenesis. Clinical presentation of this syndrome is protean ranging from minimal asymptomatic disease to life threatening bleeding and embolism. Management of this syndrome includes careful diagnosis, prevention and treatment of complications.</p></sec><sec id="st2"><title>Main observation</title><p>We are presenting a case of Klippel-Tranuanay Syndrome in a 19-year-old male patient presenting with varicosity in lateral aspect of right leg. On careful examination other components of the syndrome were found. Patient was kept on yearly follow up.</p></sec><sec id="st3"><title>Conclusion</title><p>Usually patients with Klippel-Tranuanay Syndrome present with complication. This case shows that there is also a need for medical solutions in patients who seek advise for cosmetic reasons.</p></sec></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">J Dermatol Case Rep</journal-id><journal-id journal-id-type="publisher-id">jdcr</journal-id><journal-title-group><journal-title>Journal of Dermatological Case Reports</journal-title></journal-title-group><issn pub-type="epub">1898-7249</issn><publisher><publisher-name>Specjalisci Dermatolodzy</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">21886734</article-id><article-id pub-id-type="pmc">3163347</article-id><article-id pub-id-type="doi">10.3315/jdcr.2009.1038</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>Klippel-Trenaunay Syndrome: a case report with brief review of literature</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Zea</surname><given-names>Mohammad Iqbal</given-names></name><xref ref-type="corresp" rid="COR1">*</xref></contrib><contrib contrib-type="author"><name><surname>Hanif</surname><given-names>Mohammad</given-names></name></contrib><contrib contrib-type="author"><name><surname>Habib</surname><given-names>Mohammad</given-names></name></contrib><contrib contrib-type="author"><name><surname>Ansari</surname><given-names>Ahmed</given-names></name></contrib></contrib-group><aff>Department of Surgery, Jawaharlal Nehru Medical College, Aligarh, U P, 202002, India</aff><author-notes><corresp id="COR1"><label>*</label><bold>Corresponding author:</bold> Mohammad Iqbal Zea, Department of Surgery, Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh, India. E-mail: <email>iqbal945@gmail.com</email>.
</corresp></author-notes><pub-date pub-type="collection"><day>30</day><month>12</month><year>2009</year></pub-date><pub-date pub-type="epub"><day>30</day><month>12</month><year>2009</year></pub-date><volume>3</volume><issue>4</issue><fpage>56</fpage><lpage>59</lpage><history><date date-type="received"><day>17</day><month>12</month><year>2009</year></date><date date-type="accepted"><day>20</day><month>12</month><year>2009</year></date></history><permissions><copyright-statement>Copyright: © 2009 Specjalisci Dermatolodzy</copyright-statement><copyright-year>2009</copyright-year></permissions><abstract abstract-type="executive-summary"><sec id="st1"><title>Background</title><p>Klippel-Tranuanay Syndrome is a rare sporadic disease characterized by clinical triad of capillary malformation; soft tissue and bony hypertrophy; and atypical varicosity. Although this syndrome was first described more than hundred years ago, exact incidence has not been estimated yet. Several theories have been postulated to describe its pathogenesis. Clinical presentation of this syndrome is protean ranging from minimal asymptomatic disease to life threatening bleeding and embolism. Management of this syndrome includes careful diagnosis, prevention and treatment of complications.</p></sec><sec id="st2"><title>Main observation</title><p>We are presenting a case of Klippel-Tranuanay Syndrome in a 19-year-old male patient presenting with varicosity in lateral aspect of right leg. On careful examination other components of the syndrome were found. Patient was kept on yearly follow up.</p></sec><sec id="st3"><title>Conclusion</title><p>Usually patients with Klippel-Tranuanay Syndrome present with complication. This case shows that there is also a need for medical solutions in patients who seek advise for cosmetic reasons.</p></sec></abstract><kwd-group kwd-group-type="author"><kwd>Brodie-Trendelenburg test</kwd><kwd>Klippel-Trenaunay Syndrome</kwd><kwd>Tendelenberg test</kwd><kwd>Varicose veins</kwd></kwd-group></article-meta></front></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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