﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Tabriz University of Medical Sciences</PublisherName>
      <JournalTitle>Medical Journal of Tabriz University of Medical Sciences</JournalTitle>
      <Issn>2783-2031</Issn>
      <Volume>40</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2018</Year>
        <Month>04</Month>
        <DAY>05</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Plexiform angiomyxoid myofibroblastic tumor in a 38 years old man</ArticleTitle>
    <FirstPage>97</FirstPage>
    <LastPage>100</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Akbar</FirstName>
        <LastName>Safaei</LastName>
      </Author>
      <Author>
        <FirstName>Amir</FirstName>
        <LastName>Vahedi</LastName>
      </Author>
      <Author>
        <FirstName>Leila</FirstName>
        <LastName>Vahedi</LastName>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">
      </ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>02</Month>
        <Day>05</Day>
      </PubDate>
    </History>
    <Abstract>Plexiform angiomyxoid myofibroblastic tumor is a very rare mesenchymal tumor of stomach which is diagnosed based on morphologic findings such as plexiform growth pattern, spindle cell proliferation in a myxoid background, by aiding immunohistochemistry staining and ruling out of other mesenchymal gastric tumors. We report this tumor with about 4cm size in antrum of a 38 years old man which endoscopic and CT scan results fit with Gastrointestinal stromal tumor and diagnoses is performed according to specific morphologic and immunohistochemistry findings.</Abstract>
  </Article>
</ArticleSet>