Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2005-10-13
pubmed:abstractText
We report the identification of a kaposiform hemangioendothelioma (KH) in the oropharynx of a 3-year-old boy. This is a rare endothelial-derived spindle cell neoplasm affecting children and early adolescents with features common to capillary hemangioma and Kaposi sarcoma. Nine cases of head and neck KH have been reported, this being the first in the otolaryngology literature. Our patient underwent wide local excision and has remained tumor free for over 1 year. KH should be considered in the differential diagnosis of a vascular lesion demonstrating unexpected behavior from that of a hemangioma.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0023-852X
pubmed:author
pubmed:issnType
Print
pubmed:volume
115
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1789-92
pubmed:meshHeading
pubmed:year
2005
pubmed:articleTitle
Kaposiform hemangioendothelioma: case report and literature review.
pubmed:affiliation
Department of Otolaryngology--Head and Neck Surgery, University of Texas Southwestern Medical Center, Children's Medical Center, Dallas, 75390, USA. rdefat@parknet.pmh.org
pubmed:publicationType
Journal Article, Review, Case Reports