| Literature DB >> 25489268 |
I Yonezawa1, M Waki2, Y Tamura1, R Onoda1, M Narushima1, T Ishizuka1, S Tajima3.
Abstract
Angiosarcoma is a rare and aggressive type of sarcoma, and primary angiosarcoma of the ovary is extremely rare. We report the case of a 29-year-old woman who was diagnosed with ovarian angiosarcoma and possible bone metastases. We treated this patient with a gemcitabine-based regimen as postoperative adjuvant chemotherapy, after which she achieved at least 7 years of progression-free survival, an extremely long duration given the aggressive features of this tumour. We retrospectively performed immunohistochemical analyses and fluorescence in situ hybridization to make a pathology diagnosis and to investigate the tumour features. MYC amplification and c-Myc protein overexpression were positively detected. It might be possible to correlate the effectiveness of the gemcitabine-based chemotherapeutic regimen with MYC gene amplification and c-Myc protein overexpression.Entities:
Keywords: Angiosarcoma; MYC; chemotherapy; gemcitabine; mucinous cystadenoma; surgical resection
Year: 2014 PMID: 25489268 PMCID: PMC4257124 DOI: 10.3747/co.21.2144
Source DB: PubMed Journal: Curr Oncol ISSN: 1198-0052 Impact factor: 3.677