| Literature DB >> 29689240 |
Brianna E Balansay1, Xinyuan Zhang1, Patrick D Loftus2, Joy Aparicio Valenzuela1, Eduardo Zambrano3, Anson M Lee1.
Abstract
Epithelioid hemangioendothelioma (EHE) is a rare vascular tumor that commonly affects lung, liver, and bone. Among all known EHE cases, only 20% have a pulmonary origin, with metastases to the pericardium occurring in less than 1% of these. Because of its low prevalence, variable presentation, and unknown latency period, a thoracic EHE diagnosis can be easily missed. This case outlines the unique pathologic features of EHE in a patient with cardiovascular disease, provides further insight into diagnosing a rare tumor, and provides a better understanding of the pathophysiology and progression of thoracic EHE.Entities:
Mesh:
Year: 2018 PMID: 29689240 DOI: 10.1016/j.athoracsur.2018.03.045
Source DB: PubMed Journal: Ann Thorac Surg ISSN: 0003-4975 Impact factor: 4.330