Otitis complicated by Jacod’s syndrome with unusal facial nerve involvement: Case report and review of literature

dc.contributor.authorAbdulkadir, Kocer
dc.contributor.authorBuket, Sanlisoy
dc.contributor.authorDilek, Agircan
dc.contributor.authorMünevver, Okay
dc.contributor.authorAyse, Aralasmak
dc.date.accessioned2025-05-10T15:24:17Z
dc.date.issued2015
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractOtitis media is a well-known condition and its infratemporal and intracranial complications are extremely rare because of the widespread usage of antibiotic treatment. We report a case of 63-year-old female with complaints of right-sided facial pain and diplopia. She had a history of acute otitis media before 4 months of admission to our neurology unit. Neurological examination showed that total ophthalmoplegia with ptosis, mydriasis, decreased vision and loss of pupil reflex on the right side. In addition, there was involvement of 5th and 7th cranial nerves. Neurological and radiological follow-up examinations demonstrated Jacod's Syndrome with unusual facial nerve damage and infection in aetiology. Sinusitis is the most common aetiology, but there are a few cases reported Jacod's Syndrome originating from otitis media. © 2015 Pakistan Medical Association. All rights reserved.
dc.identifier.endpage431
dc.identifier.issn0030-9982
dc.identifier.issue4
dc.identifier.pmid25976583
dc.identifier.scopus2-s2.0-84964284416
dc.identifier.scopusqualityQ3
dc.identifier.startpage429
dc.identifier.urihttps://hdl.handle.net/20.500.14730/6691
dc.identifier.volume65
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherPakistan Medical Association
dc.relation.ispartofJournal of the Pakistan Medical Association
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_Scopus_20250302
dc.subjectCranial nerve; Facial nerve; Infection; Orbital apex; Otitis; Petrous apex
dc.titleOtitis complicated by Jacod’s syndrome with unusal facial nerve involvement: Case report and review of literature
dc.typeArticle

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