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首页> 外文期刊>Journal of chemotherapy >Rapidly progressing primary splenic angiosarcoma with fatal hemorrhagic event
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Rapidly progressing primary splenic angiosarcoma with fatal hemorrhagic event

机译:快速进展的原发性脾血管肉瘤并伴有致命性出血事件

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摘要

Primary angiosarcoma of the spleen is an extremely rare malignancy. Splenic angiosarcoma is difficult to diagnose, and treatment is often challenging. The prognosis is dismal, with a mean survival of less than 1 year. Currently, no standard treatment methods have been established. Anecdotal reports suggest that early diagnosis and prompt splenectomy followed by cytotoxic chemotherapy can be effective treatment modalities. We report a case of rapidly progressing primary splenic angiosarcoma with multiple liver and bone metastases and a fatal hemorrhagic outcome.
机译:脾原发性血管肉瘤是一种极为罕见的恶性肿瘤。脾血管肉瘤难以诊断,治疗通常具有挑战性。预后不佳,平均生存期不到一年。当前,尚未建立标准的治疗方法。传闻表明,早期诊断和及时切除脾脏,然后进行细胞毒性化学疗法是有效的治疗方法。我们报告了一例快速进展的原发性脾血管肉瘤,并伴有多处肝脏和骨骼转移以及致命的出血结果。

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