<?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>42</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2004</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">"MULTIPLE GRANULAR CELL TUMOR IN A TEENAGER: REPORT OF A CASE AND REVIEW OF THE LITERATURE"</title>
    <FirstPage>228</FirstPage>
    <LastPage>231</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>J. Golchai</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>O. Zargari  MB. Paknejadi</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">Granular cell tumors are rare neoplasms of uncertain histogenesis but with a typical
histologic appearance composed of cells with characteristic granular cytoplasm. These tumors occur most often in adults as an asymptomatic solitary papule or nodule. Multiple granular cell tumors are rare, especially in children and teenagers. We represent a case of multiple granular cell tumors in a 19-year-old girl presented with multiple cutaneous and mucosal nodular lesions. The diagnosis was documented by histopathology and immunohistochemistry.</abstract>
    <web_url>https://acta.tums.ac.ir/index.php/acta/article/view/2725</web_url>
    <pdf_url>https://acta.tums.ac.ir/index.php/acta/article/download/2725/2707</pdf_url>
  </Article>
</Articles>
