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Primary splenic angiosarcoma with fever and anemia: a case report and literature review

机译:伴发烧和贫血的原发性脾血管肉瘤1例并文献复习

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摘要

Primary splenic angiosarcoma is an extremely rare and aggressive neoplasm. The prognosis of this disease is dismal, and the mean survival is less than 6 months after the diagnosis. This neoplasm typically presents with abdominal pain, splenomegaly, weight loss, and spontaneous splenic rupture. Fever is a very rare presentation of splenic angiosarcoma. Here we report the case of a 64-year-old man who presented with fever and anemia. A laparoscopic splenectomy was performed and revealed splenic angiosarcoma. The postoperative course was uneventful and the patient received 5 cycles of adjuvant chemotherapy with ifosfamide plus epirubicin. He remained disease free at 9 months after surgery. This is the first case of splenic angiosarcoma with fever as the initial presentation that was treated with laparoscopic splenectomy to be reported in the English literature.
机译:原发性脾血管肉瘤是一种极为罕见的侵袭性肿瘤。该病的预后令人沮丧,诊断后的平均生存期不到6个月。这种肿瘤通常表现为腹痛,脾肿大,体重减轻和自发性脾破裂。发烧是脾血管肉瘤非常罕见的表现。在这里,我们报告一例出现发烧和贫血的64岁男性。进行腹腔镜脾切除术,发现脾血管肉瘤。术后过程平稳,患者接受了5个周期的异环磷酰胺联合表柔比星辅助化疗。手术后9个月,他仍然没有疾病。这是第一例发烧的脾血管肉瘤,最初的表现是用腹腔镜脾切除术治疗的,这在英国文献中有报道。

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