<?xml version="1.0"?>
<Articles JournalTitle="Acta Medica Iranica">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Acta Medica Iranica</JournalTitle>
      <Issn>0044-6025</Issn>
      <Volume>28</Volume>
      <Issue>1-4</Issue>
      <PubDate PubStatus="epublish">
        <Year>1986</Year>
        <Month>12</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">KLIPPEL-TRENAUNAY SYNDEROME A CASE REPORT</title>
    <FirstPage>95</FirstPage>
    <LastPage>109</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>K. SHAMIMI</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>09</Month>
        <Day>28</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">The Klippel-Trenaunay syndrome, first reported in 1910, is a triad of cutaneous hemangioma, varicose veins, and soft tissue or bony hypertrophy. The varicosities are extensive involving the tributaries of the greater or lesser saphenous systems. Arteriogram are normal with no evidence of arteriovenous fistulas. Multiple ligation and stripping may worsen the condition, and treatment consists of wearing elastic supporting hose. A similar condition but associated with arteriovenous fistula is known as the Parkes Weber syndrome.</abstract>
    <web_url>https://acta.tums.ac.ir/index.php/acta/article/view/198</web_url>
    <pdf_url>https://acta.tums.ac.ir/index.php/acta/article/download/198/194</pdf_url>
  </Article>
</Articles>
