Online ISSN: 2149-3189
2015
Monthly
Nicaea Medical Publishing
Türkiye

Renal angiosarcoma: a rare case report

Cemil Hocazade, Mutlu Dogan, Yakup Bozkaya, Fatma Markoc
  • Cemil Hocazade (Author) Ankara Numune Education and Research Hospital, Clinic of Oncology, Ankara
  • Mutlu Dogan (Author) Ankara Numune Education and Research Hospital, Clinic of Oncology, Ankara
  • Yakup Bozkaya (Author) Ankara Numune Education and Research Hospital, Clinic of Oncology, Ankara
  • Fatma Markoc (Author) Ankara Oncology Education and Research Hospital, Clinic of Pathology, Ankara, Turkey
DOI
https://doi.org/10.18621/eurj.2015.1.1.24
Abstract
Angiosarcomas constitute about 2% of all sarcomas and generally are worst prognostic subtype of soft tissue sarcomas. Angiosarcomas are very aggressive tumors and one year after diagnosis half of patients dies with metastasis of lung, lymph nodes, bone and soft tissue. Diagnosis can accurate with immunochemistry stain, such as factor 8 related antigen, CD 31, CD 34 and von Villebrand factor. Our patient was a 61-year-old women who died four months after symptoms appeared with extensive metastasis. She was able to receive chemotherapy for only one course and after that treatment was changed to palliative.
Keywords
Angiosarcoma, renal, metastasis
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How to Cite
1.
Hocazade C, Dogan M, Bozkaya Y, Markoc F. Renal angiosarcoma: a rare case report. Eur Res J. 2015;1(1):24-28. doi:10.18621/eurj.2015.1.1.24
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Article Information

  • Article Type Case Report
  • Submitted February 21, 2026
  • Published March 3, 2015
  • Issue Vol. 1 No. 1 (2015)
  • Section Case Report
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