Chang Kenneth, Sio Terence T, Chandan Vishal S, Iott Matthew J, Hallemeier Christopher L
Department of Radiation Oncology, Mayo Clinic , Rochester, MN, USA.
Department of Anatomical Pathology, Mayo Clinic , Rochester, MN, USA.
Rare Tumors. 2014 Jan 29;6(1):5202. doi: 10.4081/rt.2014.5202. eCollection 2014 Jan 23.
Angiosarcoma of the seminal vesicle is an extremely rare malignancy, with few published case reports in the literature. We present a case of primary angiosarcoma of the seminal vesicle in a 45-year-old male who was treated with multimodality therapy, consisting of neoadjuvant chemotherapy and chemoradiation followed by surgical resection and intraoperative radiation therapy. He has been free of cancer recurrence for more than six years after completion of therapy. To our knowledge, this represents the longest reported survival of a patient with this rare tumor, and one of the few cases reported using a multimodality therapy approach.
精囊血管肉瘤是一种极为罕见的恶性肿瘤，文献中发表的病例报告很少。我们报告一例45岁男性原发性精囊血管肉瘤病例，该患者接受了多模式治疗，包括新辅助化疗和放化疗，随后进行手术切除和术中放射治疗。治疗完成后，他已无癌症复发超过六年。据我们所知，这是该罕见肿瘤患者报告的最长生存期，也是少数采用多模式治疗方法报告的病例之一。
