Surgical treatment of chylothorax caused by lymphangioleiomyomatosis
Identifieur interne : 002068 ( Pmc/Curation ); précédent : 002067; suivant : 002069Surgical treatment of chylothorax caused by lymphangioleiomyomatosis
Auteurs : Mingliang Liu ; Bingqun Wu ; Yong Cui ; Dong Chang ; Shuhong Zhang ; Min GongSource :
- Journal of Thoracic Disease [ 2072-1439 ] ; 2014.
Abstract
Lymphangioleiomyomatosis (LAM) is a rare progressive disease caused by infiltration of smooth muscle-like cells in lymph vessels as well as the lung. We report a case of pulmonary LAM in a 22-year-old female with shortness of breath, recurrent pneumothorax and chylous pleural effusions. Multiple ligation of thoracic in lower part of thoracic duct was performed and biopsy of thoracic duct confirmed the diagnosis of LAM. The operation was successful and the patient was discharged. Although the thoracic duct involvement is extensive, multiple ligation in lower part of thoracic duct may be a good choice.
Url:
DOI: 10.3978/j.issn.2072-1439.2014.01.15
PubMed: 24605238
PubMed Central: 3944183
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PMC:3944183Le document en format XML
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<author><name sortKey="Liu, Mingliang" sort="Liu, Mingliang" uniqKey="Liu M" first="Mingliang" last="Liu">Mingliang Liu</name>
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<author><name sortKey="Wu, Bingqun" sort="Wu, Bingqun" uniqKey="Wu B" first="Bingqun" last="Wu">Bingqun Wu</name>
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<author><name sortKey="Cui, Yong" sort="Cui, Yong" uniqKey="Cui Y" first="Yong" last="Cui">Yong Cui</name>
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<author><name sortKey="Chang, Dong" sort="Chang, Dong" uniqKey="Chang D" first="Dong" last="Chang">Dong Chang</name>
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<author><name sortKey="Zhang, Shuhong" sort="Zhang, Shuhong" uniqKey="Zhang S" first="Shuhong" last="Zhang">Shuhong Zhang</name>
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<author><name sortKey="Gong, Min" sort="Gong, Min" uniqKey="Gong M" first="Min" last="Gong">Min Gong</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Surgical treatment of chylothorax caused by lymphangioleiomyomatosis</title>
<author><name sortKey="Liu, Mingliang" sort="Liu, Mingliang" uniqKey="Liu M" first="Mingliang" last="Liu">Mingliang Liu</name>
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<author><name sortKey="Wu, Bingqun" sort="Wu, Bingqun" uniqKey="Wu B" first="Bingqun" last="Wu">Bingqun Wu</name>
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<author><name sortKey="Cui, Yong" sort="Cui, Yong" uniqKey="Cui Y" first="Yong" last="Cui">Yong Cui</name>
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<author><name sortKey="Chang, Dong" sort="Chang, Dong" uniqKey="Chang D" first="Dong" last="Chang">Dong Chang</name>
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<author><name sortKey="Zhang, Shuhong" sort="Zhang, Shuhong" uniqKey="Zhang S" first="Shuhong" last="Zhang">Shuhong Zhang</name>
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<author><name sortKey="Gong, Min" sort="Gong, Min" uniqKey="Gong M" first="Min" last="Gong">Min Gong</name>
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<series><title level="j">Journal of Thoracic Disease</title>
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<front><div type="abstract" xml:lang="en"><p>Lymphangioleiomyomatosis (LAM) is a rare progressive disease caused by infiltration of smooth muscle-like cells in lymph vessels as well as the lung. We report a case of pulmonary LAM in a 22-year-old female with shortness of breath, recurrent pneumothorax and chylous pleural effusions. Multiple ligation of thoracic in lower part of thoracic duct was performed and biopsy of thoracic duct confirmed the diagnosis of LAM. The operation was successful and the patient was discharged. Although the thoracic duct involvement is extensive, multiple ligation in lower part of thoracic duct may be a good choice.</p>
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<front><journal-meta><journal-id journal-id-type="nlm-ta">J Thorac Dis</journal-id>
<journal-id journal-id-type="iso-abbrev">J Thorac Dis</journal-id>
<journal-id journal-id-type="publisher-id">JTD</journal-id>
<journal-title-group><journal-title>Journal of Thoracic Disease</journal-title>
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<issn pub-type="ppub">2072-1439</issn>
<issn pub-type="epub">2077-6624</issn>
<publisher><publisher-name>Pioneer Bioscience Publishing Company</publisher-name>
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<article-id pub-id-type="publisher-id">jtd-06-02-E11</article-id>
<article-id pub-id-type="doi">10.3978/j.issn.2072-1439.2014.01.15</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Case Report</subject>
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<title-group><article-title>Surgical treatment of chylothorax caused by lymphangioleiomyomatosis</article-title>
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<contrib-group><contrib contrib-type="author"><name><surname>Liu</surname>
<given-names>Mingliang</given-names>
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<contrib contrib-type="author"><name><surname>Wu</surname>
<given-names>Bingqun</given-names>
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<contrib contrib-type="author" corresp="yes"><name><surname>Cui</surname>
<given-names>Yong</given-names>
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<contrib contrib-type="author"><name><surname>Chang</surname>
<given-names>Dong</given-names>
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<contrib contrib-type="author"><name><surname>Zhang</surname>
<given-names>Shuhong</given-names>
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<contrib contrib-type="author"><name><surname>Gong</surname>
<given-names>Min</given-names>
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<aff id="aff1">Department of Thoracic Surgery, Beijing Friendship Hospital, Capital Medical University, Beijing 100050,<country>China</country>
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<author-notes><corresp id="cor1"><italic>Corresponding to:</italic>
Yong Cui. Department of Thoracic Surgery, Beijing Friendship Hospital, Capital Medical University, 95 Yong An Road, Beijing 100050, China. E-mail: <email xlink:href="cywork1@sina.com">cywork1@sina.com</email>
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<pub-date pub-type="epub-ppub"><month>2</month>
<year>2014</year>
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<pmc-comment>Fake ppub date generated by PMC from publisher
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<pub-date pub-type="ppub"><month>2</month>
<year>2014</year>
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<volume>6</volume>
<issue>2</issue>
<fpage>E11</fpage>
<lpage>E14</lpage>
<history><date date-type="received"><day>08</day>
<month>10</month>
<year>2013</year>
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<date date-type="accepted"><day>25</day>
<month>12</month>
<year>2013</year>
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<permissions><copyright-statement>2014 Pioneer Bioscience Publishing Company. All rights reserved.</copyright-statement>
<copyright-year>2014</copyright-year>
<copyright-holder>Pioneer Bioscience Publishing Company.</copyright-holder>
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<abstract><p>Lymphangioleiomyomatosis (LAM) is a rare progressive disease caused by infiltration of smooth muscle-like cells in lymph vessels as well as the lung. We report a case of pulmonary LAM in a 22-year-old female with shortness of breath, recurrent pneumothorax and chylous pleural effusions. Multiple ligation of thoracic in lower part of thoracic duct was performed and biopsy of thoracic duct confirmed the diagnosis of LAM. The operation was successful and the patient was discharged. Although the thoracic duct involvement is extensive, multiple ligation in lower part of thoracic duct may be a good choice.</p>
</abstract>
<kwd-group kwd-group-type="author"><title>Keywords: </title>
<kwd>Lymphangioleiomyomatosis (LAM)</kwd>
<kwd>chylothorax</kwd>
<kwd>surgery</kwd>
<kwd>thoracic duct</kwd>
<kwd>biopsy</kwd>
</kwd-group>
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