Publication:
Extravascular papillary endothelial hyperplasia of the larynx: A case report and review of the literature

dc.contributor.authorsSezgin S., Kotiloǧlu E., Kaya H., Inanli S.
dc.date.accessioned2022-03-15T08:23:19Z
dc.date.accessioned2026-01-10T18:34:19Z
dc.date.available2022-03-15T08:23:19Z
dc.date.issued2005-01
dc.description.abstractPapillary endothelial hyperplasia (PEH), a tumor that falls along the spectrum of reactive to neoplastic vascular lesions, must be diagnosed carefully because it can resemble an angiosarcoma. PEH is generally considered to be the result of an unusual form of thrombus organization, exhibiting excessive papillary endothelial proliferation that is usually confined to the lumen of preexisting vessels or vascular malformations. Most cases of PEH are of the intravascular type; extravascular PEH is rare. We describe what we believe is the first reported case of an extravascular PEH in the larynx.
dc.identifier.doi10.1177/014556130508400118
dc.identifier.issn1455613
dc.identifier.pubmed15742776
dc.identifier.urihttps://hdl.handle.net/11424/248363
dc.language.isoeng
dc.publisherMedquest Communications LLC
dc.relation.ispartofEar, Nose and Throat Journal
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleExtravascular papillary endothelial hyperplasia of the larynx: A case report and review of the literature
dc.typereview
dspace.entity.typePublication
oaire.citation.endPage53
oaire.citation.issue1
oaire.citation.startPage52
oaire.citation.titleEar, Nose and Throat Journal
oaire.citation.volume84

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