Ibis K.Usta U.Cosar R.Ibis C.2024-06-122024-06-1220151757-790Xhttps://doi.org/10.1136/bcr-2014-206103https://hdl.handle.net/20.500.14551/16374Angiosarcoma 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. Copyright 2015 BMJ Publishing Group. All rights reserved.en10.1136/bcr-2014-206103info:eu-repo/semantics/openAccess(3 Iodobenzyl)Guanidine I 123; Blood Clotting Factor 8; Cd31 Antigen; Cd34 Antigen; Vimentin; Anticoagulant Agent; Warfarin; Abdominal Scintiscanning; Adult; Angiosarcoma; Article; Cancer Adjuvant Therapy; Cancer Radiotherapy; Cancer Surgery; Case Report; Computer Assisted Emission Tomography; Contrast Enhancement; External Beam Radiotherapy; Female; Follow Up; Histopathology; Human; Human Tissue; Iliac Vein; Immunohistochemistry; Middle Aged; Outcome Assessment; Tumor Localization; Vein Graft; Vein Reconstruction; Computer Assisted Tomography; Delayed Diagnosis; Fatality; Hemangiosarcoma; Iliac Vein; Male; Pathology; Prognosis; Anticoagulants; Delayed Diagnosis; Fatal Outcome; Hemangiosarcoma; Humans; Iliac Vein; Male; Middle Aged; Prognosis; Tomography, X-Ray Computed; WarfarinArticle20152-s2.0-8492166578925596292Q3