Literature DB >> 31938449

Epithelioid angiosarcoma of the liver: report of two cases and review of the literature.

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. IJCEP
Copyright © 2018.

Entities:  

Keywords:  Angiosarcoma; epithelioid angiosarcoma; hepat; metastasis

Year:  2018        PMID: 31938449      PMCID: PMC6958078     

Source DB:  PubMed          Journal:  Int J Clin Exp Pathol        ISSN: 1936-2625


  1 in total

1.  Histopathological Features of Deep Soft Tissue Epithelioid Angiosarcoma in the Lower Extremity: A Rare Case Report.

Authors:  Pham Nguyen Cuong; Nguyen Thanh Xuan; Pham Nhu Huy; Tran Nhu Tung; Nguyen Huu Son
Journal:  Am J Case Rep       Date:  2020-07-26
  1 in total

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