Angiosarcoma of common iliac vein
Identifieur interne : 001F99 ( Pmc/Curation ); précédent : 001F98; suivant : 002000Angiosarcoma of common iliac vein
Auteurs : Kamuran Ibis [Turquie] ; Ufuk Usta [Turquie] ; Rusen Cosar [Turquie] ; Cem Ibis [Turquie]Source :
- BMJ Case Reports [ 1757-790X ] ; 2015.
Abstract
Angiosarcoma is a rare malignant tumour of endothelial cells. Primary angiosarcoma of venous origin is extremely rare, and has a very poor prognosis. A 63-year-old woman with retroperitoneal mass underwent en bloc resection on a part of iliac vein followed by adjuvant radiotherapy. No recurrence was detected during 3 years of follow-up.
Url:
DOI: 10.1136/bcr-2014-206103
PubMed: 25596292
PubMed Central: 4307071
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PMC:4307071Le document en format XML
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<author><name sortKey="Ibis, Kamuran" sort="Ibis, Kamuran" uniqKey="Ibis K" first="Kamuran" last="Ibis">Kamuran Ibis</name>
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,<institution>Trakya University Medical Faculty</institution>
,<addr-line>Istanbul</addr-line>
,<country>Turkey</country>
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<country xml:lang="fr">Turquie</country>
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<author><name sortKey="Usta, Ufuk" sort="Usta, Ufuk" uniqKey="Usta U" first="Ufuk" last="Usta">Ufuk Usta</name>
<affiliation wicri:level="1"><nlm:aff id="af2"><addr-line>Department of Pathology</addr-line>
,<institution>Trakya University Medical Faculty</institution>
,<addr-line>Edirne</addr-line>
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<country xml:lang="fr">Turquie</country>
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<author><name sortKey="Cosar, Rusen" sort="Cosar, Rusen" uniqKey="Cosar R" first="Rusen" last="Cosar">Rusen Cosar</name>
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,<institution>Trakya University Medical Faculty</institution>
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<country xml:lang="fr">Turquie</country>
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<author><name sortKey="Ibis, Cem" sort="Ibis, Cem" uniqKey="Ibis C" first="Cem" last="Ibis">Cem Ibis</name>
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,<institution>Istanbul University Istanbul Medical Faculty</institution>
,<addr-line>Istanbul</addr-line>
,<country>Turkey</country>
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<country xml:lang="fr">Turquie</country>
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<author><name sortKey="Usta, Ufuk" sort="Usta, Ufuk" uniqKey="Usta U" first="Ufuk" last="Usta">Ufuk Usta</name>
<affiliation wicri:level="1"><nlm:aff id="af2"><addr-line>Department of Pathology</addr-line>
,<institution>Trakya University Medical Faculty</institution>
,<addr-line>Edirne</addr-line>
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<author><name sortKey="Cosar, Rusen" sort="Cosar, Rusen" uniqKey="Cosar R" first="Rusen" last="Cosar">Rusen Cosar</name>
<affiliation wicri:level="1"><nlm:aff id="af3"><addr-line>Department of Radiation Oncology</addr-line>
,<institution>Trakya University Medical Faculty</institution>
,<addr-line>Edirne</addr-line>
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<country xml:lang="fr">Turquie</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
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<author><name sortKey="Ibis, Cem" sort="Ibis, Cem" uniqKey="Ibis C" first="Cem" last="Ibis">Cem Ibis</name>
<affiliation wicri:level="1"><nlm:aff id="af4"><addr-line>Department of Surgery</addr-line>
,<institution>Istanbul University Istanbul Medical Faculty</institution>
,<addr-line>Istanbul</addr-line>
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<series><title level="j">BMJ Case Reports</title>
<idno type="eISSN">1757-790X</idno>
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<front><div type="abstract" xml:lang="en"><p>Angiosarcoma is a rare malignant tumour of endothelial cells. Primary angiosarcoma of venous origin is extremely rare, and has a very poor prognosis. A 63-year-old woman with retroperitoneal mass underwent en bloc resection on a part of iliac vein followed by adjuvant radiotherapy. No recurrence was detected during 3 years of follow-up.</p>
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<pmc article-type="case-report"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front><journal-meta><journal-id journal-id-type="nlm-ta">BMJ Case Rep</journal-id>
<journal-id journal-id-type="iso-abbrev">BMJ Case Rep</journal-id>
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<issn pub-type="epub">1757-790X</issn>
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<publisher-loc>BMA House, Tavistock Square, London, WC1H 9JR</publisher-loc>
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<article-id pub-id-type="pmc">4307071</article-id>
<article-id pub-id-type="publisher-id">bcr-2014-206103</article-id>
<article-id pub-id-type="doi">10.1136/bcr-2014-206103</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Article</subject>
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<subj-group subj-group-type="case-report-type"><subject>Rare Disease</subject>
</subj-group>
<subj-group subj-group-type="hwp-journal-coll"><subject>1523</subject>
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<subj-group subj-group-type="search-fields"><subject>Female</subject>
<subject>51-70 years</subject>
<subject>White</subject>
<subject>Europe (East)</subject>
</subj-group>
<series-title>Case Report</series-title>
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<title-group><article-title>Angiosarcoma of common iliac vein</article-title>
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<contrib-group><contrib contrib-type="author"><name><surname>Ibis</surname>
<given-names>Kamuran</given-names>
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<xref ref-type="aff" rid="af1">1</xref>
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<contrib contrib-type="author"><name><surname>Usta</surname>
<given-names>Ufuk</given-names>
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<xref ref-type="aff" rid="af2">2</xref>
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<contrib contrib-type="author"><name><surname>Cosar</surname>
<given-names>Rusen</given-names>
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<xref ref-type="aff" rid="af3">3</xref>
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<contrib contrib-type="author"><name><surname>Ibis</surname>
<given-names>Cem</given-names>
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<xref ref-type="aff" rid="af4">4</xref>
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<aff id="af1"><label>1</label>
<addr-line>Department of Radiation Oncology</addr-line>
,<institution>Trakya University Medical Faculty</institution>
,<addr-line>Istanbul</addr-line>
,<country>Turkey</country>
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<aff id="af2"><label>2</label>
<addr-line>Department of Pathology</addr-line>
,<institution>Trakya University Medical Faculty</institution>
,<addr-line>Edirne</addr-line>
,<country>Turkey</country>
</aff>
<aff id="af3"><label>3</label>
<addr-line>Department of Radiation Oncology</addr-line>
,<institution>Trakya University Medical Faculty</institution>
,<addr-line>Edirne</addr-line>
,<country>Turkey</country>
</aff>
<aff id="af4"><label>4</label>
<addr-line>Department of Surgery</addr-line>
,<institution>Istanbul University Istanbul Medical Faculty</institution>
,<addr-line>Istanbul</addr-line>
,<country>Turkey</country>
</aff>
<author-notes><corresp><label>Correspondence to</label>
Dr Kamuran Ibis, <email>kamuranibis@gmail.com</email>
</corresp>
</author-notes>
<pub-date pub-type="collection"><year>2015</year>
</pub-date>
<pub-date pub-type="epub"><day>16</day>
<month>1</month>
<year>2015</year>
</pub-date>
<volume>2015</volume>
<elocation-id>bcr2014206103</elocation-id>
<history><date date-type="accepted"><day>30</day>
<month>12</month>
<year>2014</year>
</date>
</history>
<permissions><copyright-statement>2015 BMJ Publishing Group Ltd</copyright-statement>
<copyright-year>2015</copyright-year>
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<self-uri xlink:title="pdf" xlink:href="bcr-2014-206103.pdf"></self-uri>
<abstract><p>Angiosarcoma is a rare malignant tumour of endothelial cells. Primary angiosarcoma of venous origin is extremely rare, and has a very poor prognosis. A 63-year-old woman with retroperitoneal mass underwent en bloc resection on a part of iliac vein followed by adjuvant radiotherapy. No recurrence was detected during 3 years of follow-up.</p>
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