﻿<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.0//EN" "http://www.ncbi.nlm.nih.gov:80/entrez/query/static/PubMed.dtd"[]>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Science and Education Publishing</PublisherName>
      <JournalTitle>American Journal of Medical Case Reports</JournalTitle>
      <Issn>2374-216X</Issn>
      <Volume>4</Volume>
      <Issue>6</Issue>
      <PubDate PubStatus="epublish">
        <Year>2016</Year>
        <Month>6</Month>
        <Day>25</Day>
      </PubDate>
    </Journal>
    <ArticleTitle>Chondroblastoma of Diaphysis of Tibia; Case Report</ArticleTitle>
    <FirstPage>215</FirstPage>
    <LastPage>217</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Heidarali</FirstName>
        <LastName>Esmaeili</LastName>
      </Author>
      <Author>
        <FirstName>Haniyeh</FirstName>
        <LastName>Amidfar</LastName>
        <Affiliation>Assissstant of Pathology, Iran</Affiliation>
      </Author>
      <Author>
        <FirstName>Mehrdad</FirstName>
        <LastName>Yavarikia</LastName>
      </Author>
      <Author>
        <FirstName>Atiyeh</FirstName>
        <LastName>Amidfar</LastName>
      </Author>
    </AuthorList>
    <ArticleIdList>
      <ArticleId IdType="pii">AJMCR2016468</ArticleId>
      <ArticleId IdType="doi">10.12691/ajmcr-4-6-8</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2016</Year>
        <Month>2</Month>
        <Day>28</Day>
      </PubDate>
      <PubDate PubStatus="revised">
        <Year>2016</Year>
        <Month>4</Month>
        <Day>19</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2016</Year>
        <Month>6</Month>
        <Day>23</Day>
      </PubDate>
    </History>
    <Abstract>Background: Chondroblastoma is a rare benign cartilaginous neoplasm that considered for approximately 1% of all bone tumors and characteristically emerges in the epiphysis of a long bone, especially the hummeros, femurand tibia.Only rare cases have been reported in the diaphyseal region. Case Report: We report a case of diaphyseal one in a 13 years old girl that admitted ith brief pain and deformities in left leg. Radiographic examinations disclosed a multiloculated osteolytic lesion in left tibia. Conclusion: Histologicak findings revealed proliferation of polygonal cells in the cartigenous background with few Giant cells.</Abstract>
  </Article>
</ArticleSet>