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<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>5</Issue>
      <PubDate PubStatus="epublish">
        <Year>2016</Year>
        <Month>5</Month>
        <Day>30</Day>
      </PubDate>
    </Journal>
    <ArticleTitle>Tension Pneumothorax as the Presentation of Pulmonary Langerhans Histiocytosis</ArticleTitle>
    <FirstPage>173</FirstPage>
    <LastPage>174</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Conor</FirstName>
        <LastName>McCartney</LastName>
        <Affiliation>Department Internal Medicine, St. Louis University, United States</Affiliation>
      </Author>
      <Author>
        <FirstName>Andrew</FirstName>
        <LastName>Freeman</LastName>
      </Author>
      <Author>
        <FirstName>Ravi</FirstName>
        <LastName>Nayak</LastName>
        <Affiliation>Internal Medicine, Program Director Division of Pulmonary, Critical Care and Sleep Medicine, St. Louis University, United States</Affiliation>
      </Author>
    </AuthorList>
    <ArticleIdList>
      <ArticleId IdType="pii">AJMCR2016458</ArticleId>
      <ArticleId IdType="doi">10.12691/ajmcr-4-5-8</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>12</Month>
        <Day>29</Day>
      </PubDate>
      <PubDate PubStatus="revised">
        <Year>2016</Year>
        <Month>4</Month>
        <Day>5</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2016</Year>
        <Month>5</Month>
        <Day>28</Day>
      </PubDate>
    </History>
    <Abstract>A 36 year old male smoker presented to the emergency department with shortness of breath. A chest x-ray showed a tension pneumothorax. Chest tube was placed urgently. CT scan showed upper lobe predominant cystic lung lesions. Biopsy confirmed the diagnosis of pulmonary Langerhans Histiocytosis.</Abstract>
  </Article>
</ArticleSet>