Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2010-8-12
pubmed:abstractText
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.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1863-6713
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
58
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
431-3
pubmed:meshHeading
pubmed:year
2010
pubmed:articleTitle
Surgical resection of a primary pulmonary epithelioid hemangioendothelioma in bilateral lungs.
pubmed:affiliation
Department of Thoracic Surgery, Matsuyama Red Cross Hospital, 1-Banchi, Bunkyo-cho, Matsuyama, Ehime, 790-8524, Japan. evergreen_field_1633@matsuyama.jrc.or.jp
pubmed:publicationType
Journal Article, Case Reports