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<Articles JournalTitle="Journal of Craniomaxillofacial Research">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Journal of Craniomaxillofacial Research</JournalTitle>
      <Issn>2345-5489</Issn>
      <Volume>10</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="epublish">
        <Year>2024</Year>
        <Month>03</Month>
        <Day>03</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Solitary Intraosseous Neurofibroma Of Mandible: A Case Report</title>
    <FirstPage>208</FirstPage>
    <LastPage>211</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Amir</FirstName>
        <LastName>Abbasi</LastName>
        <affiliation locale="en_US">Department of Oral and Maxillofacial Surgery, Sina Hospital, Tehran University Of Medical Sciences, Tehran, Iran; Craniomaxillofacial Research Center, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Pouyan</FirstName>
        <LastName>Aminishakib</LastName>
        <affiliation locale="en_US">Department of Oral and Maxillofacial Pathology, School of Dentistry, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mani</FirstName>
        <LastName>Arashrad</LastName>
        <affiliation locale="en_US">Craniomaxillofacial Research Center, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2024</Year>
        <Month>02</Month>
        <Day>13</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2024</Year>
        <Month>02</Month>
        <Day>13</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Neurofibroma is a benign tumor derived from the peripheral nerve. Most of these can be multifocal as a component of neurofibromatosis or present as a solitary tumor. Although the solitary neurofibroma is not an uncommon lesion, its intraosseous occurrence is rare, and less than 50 cases have been reported. We report a rare case of central neurofibroma, arising in the mandibular bone of 57-year-old edentulous female patient on the left side. Hemi mandibulectomy was performed and reconstructed with a reconstruction plate without any bone graft. Microscopic evaluation showed neoplastic tissue with haphazardly arranged and interlacing fascicular patterns composed of point-ended spindle-shaped tumoral cells. Immunohistochemical examination of the tumor showed positive staining for S-100 protein antibodies.
Keywords: Intraosseous neurofibroma; Mandible.</abstract>
    <web_url>https://jcr.tums.ac.ir/index.php/jcr/article/view/490</web_url>
    <pdf_url>https://jcr.tums.ac.ir/index.php/jcr/article/download/490/399</pdf_url>
  </Article>
</Articles>
