Angiosarcoma of common iliac vein
Küçük Resim Yok
Tarih
2015
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
BMJ Publishing Group
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
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. Copyright 2015 BMJ Publishing Group. All rights reserved.
Açıklama
Anahtar Kelimeler
(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; Warfarin
Kaynak
BMJ Case Reports
WoS Q Değeri
Scopus Q Değeri
Q3
Cilt
2015
