| Literature DB >> 28104995 |
Jun-Wu Yang1, Yong Li1, Kai Xie1, Wei Dong1, Xian-Tong Cao1, Wei-Dong Xiao1.
Abstract
Hepatic epithelioid hemangioendothelioma (HEH) is a rare tumor of vascular endothelial origin. Spontaneous rupture of HEH is a life-threatening complication and is extremely rare. HEH has variable malignant potential, and the clinical diagnosis remains challenging. Here we report a case of HEH with spontaneous rupture. A 44-year-old man presented with constant cutting pains over the right upper abdomen after eating. He had hemoptysis 11 d previously. Diagnostic abdominal puncture demonstrated active bleeding. Chest and abdominal computer tomography scan showed multiple ground-glass nodules over the lungs, multiple low-density intrahepatic nodules and massive hemorrhage. Transcatheter arterial embolization and exploratory laparotomy were performed and subsequent immunohistochemical examination confirmed a diagnosis of HEH.Entities:
Keywords: Hepatic epithelioid hemangioendothelioma; Spontaneous rupture
Mesh:
Substances:
Year: 2017 PMID: 28104995 PMCID: PMC5221283 DOI: 10.3748/wjg.v23.i1.185
Source DB: PubMed Journal: World J Gastroenterol ISSN: 1007-9327 Impact factor: 5.742