<?xml version="1.0"?>
<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>2026</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2026</Year>
        <Month>08</Month>
        <Day>25</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Maxillary Osteoblastoma in a Child Mimicking Intraosseous  Hemangioma: A Case Report</title>
    <FirstPage>228</FirstPage>
    <LastPage>232</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Bahareh</FirstName>
        <LastName>Fattahi</LastName>
        <affiliation locale="en_US">Department of Oral and Maxillofacial Pathology, School of Dentistry, Kashan University of Medical Sciences, Kashan, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Arash</FirstName>
        <LastName>Esmaeili</LastName>
        <affiliation locale="en_US">Department of Oral and Maxillofacial Surgery, School of Dentistry, Isfahan University of Medical Sciences, Isfahan, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Hasti</FirstName>
        <LastName>Sarabi Kia</LastName>
        <affiliation locale="en_US">Department of Oral and Maxillofacial Surgery, School of Dentistry, Isfahan University of Medical Sciences, Isfahan, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2026</Year>
        <Month>05</Month>
        <Day>12</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2026</Year>
        <Month>07</Month>
        <Day>04</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Maxillary osteoblastoma in children is exceptionally rare, accounting for fewer than 5% of all craniofacial cases. This benign bone tumor can closely mimic intraosseous hemangioma both clinically and radiographically due to its highly vascular stroma, leading to diagnostic pitfalls. We report a 5-year-old girl whose maxillary lesion exhibited soft, fluctuant swelling, reddish discoloration, bleeding on touch, and post-extraction hemorrhage&#x2014;features strongly suggestive of hemangioma. A multidisciplinary approach involving maxillofacial surgery, radiology, and pathology was essential for definitive diagnosis. This case underscores that osteoblastoma must remain in the differential diagnosis of vascular-appearing pediatric maxillary masses, and multidisciplinary collaboration is critical to avoid misdiagnosis.&#xA0;
Keywords: Osteoblastoma; Maxilla; Hemangioma.</abstract>
    <web_url>https://jcr.tums.ac.ir/index.php/jcr/article/view/648</web_url>
    <pdf_url>https://jcr.tums.ac.ir/index.php/jcr/article/download/648/501</pdf_url>
  </Article>
</Articles>
