| Literature DB >> 20703867 |
Hiromitsu Baba1, Makiko Tomiyasu, Hideki Makino, Akihiko Yamamoto, Hideki Yokoyama, Yumi Oshiro.
Abstract
Pulmonary epithelioid hemangioendothelioma (PEH) is a rare pulmonary neoplasm that was initially described in 1975 as an intravascular bronchioloalveolar tumor. This report presents the case of a patient with multifocal primary pulmonary PEH (11 tumors) in the bilateral lungs. All of the tumors detected in the preoperative computed tomography scan were surgically resected. The patient has been doing well for 9 years after surgery. No tumor recurred for 8 years after surgery until a single recurrent nodule appeared and was thoracoscopically resected.Entities:
Mesh:
Year: 2010 PMID: 20703867 DOI: 10.1007/s11748-009-0546-6
Source DB: PubMed Journal: Gen Thorac Cardiovasc Surg ISSN: 1863-6705