Maier A, Bataille F, Krenz D, Anthuber M
Klinik und Poliklinik für Chirurgie, Universität Regensburg.
Chirurg. 2004 Jan;75(1):70-4. doi: 10.1007/s00104-003-0733-4.
A splenectomy was performed in a 37-year-old woman because of spontaneous rupture of the spleen. Primary angiosarcoma of the spleen was diagnosed postoperatively based on histology. Primary angiosarcoma of the spleen is a very rare neoplasm with disastrous prognosis. Immunohistochemical and ultrastructural examinations are necessary to verify the diagnosis because the histopathological picture of the tumor is variable. Due to the small number of reported cases, there are no guidelines for adjuvant or palliative therapy, and up to today all adjuvant means of radiotherapy and chemotherapy have not improved the prognosis of the patients.
一名37岁女性因脾脏自发性破裂接受了脾切除术。术后根据组织学诊断为脾脏原发性血管肉瘤。脾脏原发性血管肉瘤是一种非常罕见的肿瘤,预后很差。由于肿瘤的组织病理学表现多变,因此需要进行免疫组织化学和超微结构检查来确诊。由于报道的病例数量较少,目前尚无辅助或姑息治疗的指南,迄今为止,所有放疗和化疗等辅助手段均未改善患者的预后。