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Erdheim-Chester disease presented with bilateral carotid artery occlusion: Case report

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dc.contributor.authorsÇelik Y., Balci K., Asil T., Tüzün E., Hamamcioǧlu M.K., Temizöz O., Albayram S., Sav A.
dc.date.accessioned2022-03-28T14:57:49Z
dc.date.accessioned2026-01-11T15:27:21Z
dc.date.available2022-03-28T14:57:49Z
dc.date.issued2010
dc.description.abstractErdheim-Chester disease is a rare, non-Langerhans form of systemic histiocytosis of unknown etiology. The disease affects multiple organ systems, including musculoskeletal, cardiac, pulmonary, gastrointestinal, and central nervous systems, producing protean manifestations. Neurological manifestations are less frequent. We present a 44-year-old patient with Erdheim-Chester disease who had bilateral carotid artery occlusion and cavernous sinus infiltration.
dc.identifier.issn1301062X
dc.identifier.urihttps://hdl.handle.net/11424/256489
dc.language.isoeng
dc.relation.ispartofTurk Noroloji Dergisi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectCarotid arteries
dc.subjectErdheim-Chester disease
dc.subjectOphthalmoplegia
dc.titleErdheim-Chester disease presented with bilateral carotid artery occlusion: Case report
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage113
oaire.citation.issue2
oaire.citation.startPage110
oaire.citation.titleTurk Noroloji Dergisi
oaire.citation.volume16

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