<?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>7</Issue>
<PubDate PubStatus="epublish">
<Year>2016</Year>
<Month>7</Month>
<Day>26</Day>
</PubDate>
</Journal>
<ArticleTitle>Myelofibrosis with Tuberculosis: A Case Report</ArticleTitle>
<FirstPage>240</FirstPage>
<LastPage>241</LastPage>
<Language>EN</Language>
<AuthorList>
<Author>
<FirstName>YK</FirstName>
<LastName>Jin</LastName>
</Author>
<Author>
<FirstName>QL</FirstName>
<LastName>Shi</LastName>
</Author>
<Author>
<FirstName>CH</FirstName>
<LastName>Peng</LastName>
</Author>
<Author>
<FirstName>H</FirstName>
<LastName>Yu</LastName>
</Author>
<Author>
<FirstName>XY</FirstName>
<LastName>Zhang</LastName>
</Author>
<Author>
<FirstName>XW</FirstName>
<LastName>Ye</LastName>
<Affiliation>Guizhou Provincial People's hospital, Guiyang, China</Affiliation>
</Author>

</AuthorList>
<ArticleIdList>
<ArticleId IdType="pii">AJMCR2016476</ArticleId>
<ArticleId IdType="doi">10.12691/ajmcr-4-7-6</ArticleId>
</ArticleIdList>
<History>
<PubDate PubStatus="received">
<Year>2016</Year>
<Month>4</Month>
<Day>8</Day>
</PubDate>
<PubDate PubStatus="revised">
<Year>2016</Year>
<Month>6</Month>
<Day>15</Day>
</PubDate>
<PubDate PubStatus="accepted">
<Year>2016</Year>
<Month>7</Month>
<Day>24</Day>
</PubDate>
</History>
<Abstract>Myelofibrosis (MF), or fibrosis of the bone marrow, is an uncommon condition. Most cases arise secondary to other disease processes. However, whether tuberculosis can stimulate a secondary fibrotic reaction or develop in patients who have preexisting myeloproliferative disorders is not clear. Here we present a case of a 54-year-old man whose myelofibrosis disappeared completely after administration of antituberculous treatment. The purpose of reporting this case is to reconsider the relationship between tuberculosis and secondary myelofibrosis.</Abstract>
</Article>
</ArticleSet>
