Angiosarcoma of common iliac vein
Identifieur interne : 002148 ( Main/Merge ); précédent : 002147; suivant : 002149Angiosarcoma 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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,<country>Turkey</country>
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<country xml:lang="fr">Turquie</country>
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<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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<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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