Terada T, Nakanuma Y, Matsubara T, Suematsu T
Second Department of Pathology, Kanazawa University School of Medicine, Japan.
Acta Pathol Jpn. 1988 Oct;38(10):1345-51. doi: 10.1111/j.1440-1827.1988.tb02285.x.
The pathology of a rare case of primary diffuse angiosarcoma of the pericardium is reported. Grossly, the heart was entirely encased by the pericardial tumor, and the myocardium was only superficially invaded by the tumor. The tumor tissue extended directly to the mediastinum, where the great vessels were embedded in the tumor. A few minute distant metastases were found only in the bilateral lungs and pulmonary hilar lymph nodes. Microscopically, the tumor tissue was composed of malignant cells forming vascular channels admixed with solid areas. Histo- and immunohistochemically, no mesothelial characteristics were evident. Factor VIII-related antigen and Ulex europaeus I lectin were positive, implying that the tumor was of vascular origin. Grossly, and in part microscopically, this case resembled malignant diffuse mesothelioma, indicating that pericardial angiosarcoma may sometimes mimick malignant mesothelioma.
报告了一例罕见的心包原发性弥漫性血管肉瘤的病理学情况。大体上,心脏完全被心包肿瘤包裹,心肌仅被肿瘤浅表侵犯。肿瘤组织直接延伸至纵隔,大血管包埋于肿瘤之中。仅在双侧肺和肺门淋巴结发现了少数微小的远处转移灶。显微镜下,肿瘤组织由形成血管腔隙并伴有实性区域的恶性细胞组成。组织学和免疫组织化学检查显示,未发现明显的间皮特征。VIII因子相关抗原和荆豆凝集素I呈阳性,提示肿瘤起源于血管。大体和部分显微镜下表现,该病例类似于恶性弥漫性间皮瘤,表明心包血管肉瘤有时可能会模仿恶性间皮瘤。