Deng Rui, Chang Weilong, Wu Xiuli, Chen Junhua, Tao Kaixiong, Zhang Peng
Department of Gastrointestinal Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan, China.
Department of Pathology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan, China.
Int J Clin Exp Pathol. 2015 Nov 1;8(11):14040-4. eCollection 2015.
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.
原发性脾血管肉瘤是一种极其罕见且侵袭性强的肿瘤。这种疾病的预后很差,诊断后的平均生存期不到6个月。该肿瘤通常表现为腹痛、脾肿大、体重减轻和自发性脾破裂。发热是脾血管肉瘤非常罕见的表现。在此我们报告一例64岁男性患者,其以发热和贫血就诊。行腹腔镜脾切除术,术后病理显示为脾血管肉瘤。术后过程顺利,患者接受了5个周期的异环磷酰胺加表柔比星辅助化疗。术后9个月时他仍无疾病复发。这是英文文献中报道的首例以发热为首发表现并接受腹腔镜脾切除术治疗的脾血管肉瘤病例。