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<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.1 20151215//EN" "JATS-journalpublishing1.dtd">
<article xml:lang="KO" article-type="case-report">

<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Tuberc Respir Dis</journal-id>
<journal-id journal-id-type="publisher-id">TRD</journal-id>
<journal-title-group>
<journal-title>Tuberculosis and Respiratory Diseases</journal-title>
</journal-title-group>
<issn pub-type="ppub">0378-0066</issn>
<publisher>
<publisher-name>The Korean Academy of Tuberculosis and Respiratory Diseases</publisher-name>
</publisher>
</journal-meta>

<article-meta>
<article-id pub-id-type="doi">10.4046/trd.2003.55.1.107</article-id>
<article-categories>
<subj-group>
<subject>Case Report</subject>
</subj-group>
</article-categories>

<title-group>
<article-title>A Case of Congenital Cystic Adenomatoid Malformation(CCAM) of the Lung in Adult</article-title>
</title-group>

<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Cho</surname>
<given-names>Yongsoen</given-names>
</name>
<degrees>M.D.</degrees>
<xref ref-type="aff" rid="A1"></xref>
</contrib>

<contrib contrib-type="author">
<name>
<surname> Lee</surname>
<given-names>Yang Duk</given-names>
</name>
<degrees>M.D.</degrees>
<xref ref-type="aff" rid="A1"></xref>
</contrib>

<contrib contrib-type="author">
<name>
<surname>Han</surname>
<given-names>Minsoo</given-names>
</name>
<degrees>M.D.</degrees>
<xref ref-type="aff" rid="A1"></xref>
</contrib>

<contrib contrib-type="author">
<name>
<surname>Kang</surname>
<given-names>Tong Uk</given-names>
</name>
<degrees>M.D.</degrees>
<xref ref-type="aff" rid="A2">*</xref>
</contrib>

</contrib-group>

<aff id="A1">Department of Internal Medicine, School of Medicine, Eulji University, Daejeon, Korea.</aff>
<aff id="A2"><label>*</label>Department of Pathology, School of Medicine, Eulji University, Daejeon, Korea.</aff>

<author-notes>
<corresp>
Address for correspondence: Yongseon Cho, M.D. Department of Internal medicine, School of Medicine, Eulji University 24-14, Moek dong, Joong-gu, Daejeon, Korea. Phone: 042-259-1203, Fax: 042-259-1207, <email>casimirus@chollian.net</email>
</corresp>
</author-notes>

<pub-date pub-type="ppub">
<month>07</month>
<year>2003</year>
</pub-date>
<pub-date pub-type="epub">
<day>31</day>
<month>07</month>
<year>2003</year>
</pub-date>
<volume>55</volume>
<issue>1</issue>
<fpage>107</fpage>
<lpage>112</lpage>
<permissions>
<copyright-statement>Copyright&#x00A9;2003. The Korean Academy of Tuberculosis and Respiratory Diseases. All rights reserved.</copyright-statement>
<copyright-year>2003</copyright-year>
</permissions>

<abstract>
<p> A congenital cystic adenoid malformation of the lung(CCAM) is characterized by an anomalous fetal development of the terminal respiratory structures, resulting in the adenomatoid proliferation of the bronchiolar elements and cystic formation. CCAM has been detected on the fetus, premature babies and stillborn as well as infants and children. An adult presentation of CCAM is extremely rare. When cystic lesions occur with a repeated infection, an evaluation of the cystic lesions requires a differential diagnosis of CCAM, sequestration, a lung abscess, a pneumatocele and a bronchogenic cyst. The definite treatment of CCAM is the surgical removal of the involved lobe. We report a case of a CCAM in a 24-year-old female with a brief review of the relevant literature.</p>
</abstract>

<kwd-group>
<kwd>Congenital cystic adenoid malformation</kwd>
<kwd>Lung cysts</kwd>
<kwd>Lung anomalities</kwd>
</kwd-group>

</article-meta>
</front>
</article>


