McGinley K, Googe P, Hanna W, Bell J
Department of Pathology, University of Tennessee Medical Center at Knoxville 37920, USA.
South Med J. 1995 Aug;88(8):873-5. doi: 10.1097/00007611-199508000-00020.
We describe a 47-year-old man with shoulder pain, multiple bony lesions, and a 1-cm lesion in the spleen. T-1 facetectomy revealed a poorly differentiated malignant neoplasm. Several months after chemotherapy, multiple splenic lesions were found by computed tomography and liver-spleen scan. A splenectomy showed a malignant spindle-cell neoplasm forming irregular vascular spaces. Tumor cells were positive for factor VIII-related antigen and vimentin. This patient died of extensive metastases from this primary angiosarcoma of the spleen. Splenic angiosarcoma is a rare neoplasm that often has a cryptic presentation and a dismal prognosis.
我们描述了一名47岁男性,有肩部疼痛、多处骨病变以及脾脏内一个1厘米的病变。T-1节段切除术显示为低分化恶性肿瘤。化疗数月后,计算机断层扫描和肝脾扫描发现脾脏有多处病变。脾切除术显示为恶性梭形细胞瘤,形成不规则血管腔隙。肿瘤细胞对因子VIII相关抗原和波形蛋白呈阳性。该患者死于脾脏原发性血管肉瘤的广泛转移。脾血管肉瘤是一种罕见肿瘤,通常表现隐匿,预后不佳。