PDF(Pubmed)
Abstract：
Primary hepatic angiosarcoma (PHA) is an exceedingly rare and aggressive neoplasm of mesenchymal origin. PHA makes a very small portion of primary liver tumors and conveys a poor prognosis. Symptomatology can be vague and often mimics primary hepatocellular carcinoma upon presentation. Diagnosis requires careful immunohistopathologic confirmation. We present a case of PHA in a patient with abdominal pain and suspected underlying cryptogenic cirrhosis.
摘要：
原发性肝血管肉瘤（PHA）是一种极为罕见且侵袭性的间充质起源肿瘤。PHA占原发性肝肿瘤的很小一部分，预后较差。症状可能是模糊的，并且通常在出现时模仿原发性肝细胞癌。诊断需要仔细的免疫组织病理学确认。我们介绍了一名患有腹痛和怀疑潜在隐源性肝硬化的患者的PHA病例。
