| Literature DB >> 31938449 |
Manmei Long1, Wumairehan Shali2, Qiongyi Huang3, Yongyang Bao1, Ying Chen1, Yaming Rao1, Henghua Zhou1, Qiang Liu4, Qiao He4, Chuyi Zheng4, Wenyong Liu2, Yanbo Zhu1.
Abstract
Angiosarcoma is a malignant tumor of endothelial origin. Epithelioid angiosarcoma is a subtype of angiosarcoma, in which the malignant endothelial cells have a predominantly epithelioid appearance. So far, few cases of primary hepatic epithelioid andiosarcoma (PHEA) have been described. In this case report, we describe two rare cases of PHEA. Microscopically, the tumors were consistently composed of atypical epithelioid cells with vesicular nuclei, prominent nucleoli, and eosinophilic cytoplasm. One patient had metastatic disease and underwent palliative hepatic surgery following radiotherapy and chemotherapy, and had a postoperative survival time of 12 months, while the other patient is still alive after tumor resection. PHEA is an aggressive malignant tumor with a high rate of metastasis. IJCEPEntities:
Keywords: Angiosarcoma; epithelioid angiosarcoma; hepat; metastasis
Year: 2018 PMID: 31938449 PMCID: PMC6958078
Source DB: PubMed Journal: Int J Clin Exp Pathol ISSN: 1936-2625