Giant Diaphragmatic Angiosarcoma of Adult: A Case Report and Review of Literature
Identifieur interne : 002136 ( Pmc/Curation ); précédent : 002135; suivant : 002137Giant Diaphragmatic Angiosarcoma of Adult: A Case Report and Review of Literature
Auteurs : Tao Ren ; Xue-Qian Chen [République populaire de Chine]Source :
- Case Reports in Medicine [ 1687-9627 ] ; 2012.
Abstract
Angiosarcoma is a rare vascular malignant soft tissue tumor, with highly malignant, invasive, and multifocal characteristics of biology, which is prone to local recurrence and distant metastasis, so the prognosis is extremely poor. It rarely involves the diaphragm. We present the case of an adult patient who had a primary giant angiosarcoma of the left-sided diaphragm.
Url:
DOI: 10.1155/2012/950856
PubMed: 22431944
PubMed Central: 3295565
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<author><name sortKey="Chen, Xue Qian" sort="Chen, Xue Qian" uniqKey="Chen X" first="Xue-Qian" last="Chen">Xue-Qian Chen</name>
<affiliation wicri:level="1"><nlm:aff id="I3">Department of Clinical Medicine, North Sichuan Medical College, Nanchong 637000, China</nlm:aff>
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<front><div type="abstract" xml:lang="en"><p>Angiosarcoma is a rare vascular malignant soft tissue tumor, with highly malignant, invasive, and multifocal characteristics of biology, which is prone to local recurrence and distant metastasis, so the prognosis is extremely poor. It rarely involves the diaphragm. We present the case of an adult patient who had a primary giant angiosarcoma of the left-sided diaphragm.</p>
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<front><journal-meta><journal-id journal-id-type="nlm-ta">Case Rep Med</journal-id>
<journal-id journal-id-type="iso-abbrev">Case Rep Med</journal-id>
<journal-id journal-id-type="publisher-id">CRIM</journal-id>
<journal-title-group><journal-title>Case Reports in Medicine</journal-title>
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<issn pub-type="ppub">1687-9627</issn>
<issn pub-type="epub">1687-9635</issn>
<publisher><publisher-name>Hindawi Publishing Corporation</publisher-name>
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<article-meta><article-id pub-id-type="pmid">22431944</article-id>
<article-id pub-id-type="pmc">3295565</article-id>
<article-id pub-id-type="doi">10.1155/2012/950856</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Case Report</subject>
</subj-group>
</article-categories>
<title-group><article-title>Giant Diaphragmatic Angiosarcoma of Adult: A Case Report and Review of Literature</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Ren</surname>
<given-names>Tao</given-names>
</name>
<xref ref-type="aff" rid="I1"><sup>1, 2</sup>
</xref>
<xref ref-type="aff" rid="I2"></xref>
<xref ref-type="corresp" rid="cor1">*</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Chen</surname>
<given-names>Xue-qian</given-names>
</name>
<xref ref-type="aff" rid="I3"><sup>3</sup>
</xref>
</contrib>
</contrib-group>
<aff id="I1"><sup>1</sup>
Department of Oncology, The Affiliated Hospital, North Sichuan Medical College, Nanchong 637000, China</aff>
<aff id="I2"><sup>2</sup>
Key Disciplines of Oncology in Sichuan Province, The Affiliated Hospital, North Sichuan Medical College, Nanchong 637000, China</aff>
<aff id="I3"><sup>3</sup>
Department of Clinical Medicine, North Sichuan Medical College, Nanchong 637000, China</aff>
<author-notes><corresp id="cor1">*Tao Ren: <email>584239854@qq.com</email>
</corresp>
<fn fn-type="other"><p>Academic Editor: Lothar Bergmann</p>
</fn>
</author-notes>
<pub-date pub-type="ppub"><year>2012</year>
</pub-date>
<pub-date pub-type="epub"><day>1</day>
<month>2</month>
<year>2012</year>
</pub-date>
<volume>2012</volume>
<elocation-id>950856</elocation-id>
<history><date date-type="received"><day>3</day>
<month>9</month>
<year>2011</year>
</date>
<date date-type="accepted"><day>28</day>
<month>10</month>
<year>2011</year>
</date>
</history>
<permissions><copyright-statement>Copyright © 2012 T. Ren and X.-q. Chen.</copyright-statement>
<copyright-year>2012</copyright-year>
<license xlink:href="https://creativecommons.org/licenses/by/3.0/"><license-p>This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<abstract><p>Angiosarcoma is a rare vascular malignant soft tissue tumor, with highly malignant, invasive, and multifocal characteristics of biology, which is prone to local recurrence and distant metastasis, so the prognosis is extremely poor. It rarely involves the diaphragm. We present the case of an adult patient who had a primary giant angiosarcoma of the left-sided diaphragm.</p>
</abstract>
</article-meta>
</front>
<floats-group><fig id="fig1" position="float"><label>Figure 1</label>
<caption><p>CT findings of angiosarcoma of the diaphragm (tumors were located under the chest, a huge volume, heterogeneous enhancement, No mediastinal lymph nodes).</p>
</caption>
<graphic xlink:href="CRIM2012-950856.001"></graphic>
</fig>
<fig id="fig2" position="float"><label>Figure 2</label>
<caption><p>Histopathological microscopic structure of diaphragm angiosarcoma (tumor cell atypia, abnormal vessel-like cavities structure).</p>
</caption>
<graphic xlink:href="CRIM2012-950856.002"></graphic>
</fig>
<fig id="fig3" position="float"><label>Figure 3</label>
<caption><p>Epithelioid cells strongly positive with CD34 (×200).</p>
</caption>
<graphic xlink:href="CRIM2012-950856.003"></graphic>
</fig>
</floats-group>
</pmc>
</record>
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