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Idiopathic intracranial hypertension presenting as bilateral spontaneous lateral intrasphenoidal and transethmoidal meningoceles: a case report and review of the literature

dc.contributor.authorRadonjic, Aleksandar
dc.contributor.authorKassab, Abdul M
dc.contributor.authorMoldovan, Ioana D
dc.contributor.authorKilty, Shaun
dc.contributor.authorAlkherayf, Fahad
dc.date.accessioned2019-03-11T17:02:19Z
dc.date.available2019-03-11T17:02:19Z
dc.date.issued2019-03-05
dc.date.updated2019-03-11T17:02:20Z
dc.description.abstractAbstract Background Basal meningoceles are rare herniations of the meninges that tend to present unilaterally with cerebrospinal fluid rhinorrhea. Growing evidence suggests that intracranial hypertension contributes considerably to the formation of spontaneous basal meningoceles. Case presentation A 50-year-old man of Middle East ethnicity presented with a 16-week history of cerebrospinal fluid rhinorrhea, short-term memory loss, and slight decline in cognitive function. We present a case of bilateral spontaneous meningoceles with bone defects in the left lateral sphenoid sinus and right anterior cribriform plate, as well as with a remodeled sella. A neuronavigation-assisted expanded endoscopic endonasal surgery was performed to resect the meningoceles. Postoperative imaging demonstrated complete resolution of the bilateral meningoceles. Conclusions This case reports the first bilateral basal spontaneous meningoceles in the literature. Furthermore, based on this case’s imaging results and the literature reviewed, elevated intracranial pressure may be a determining factor behind the development of spontaneous meningoceles.
dc.identifier.citationJournal of Medical Case Reports. 2019 Mar 05;13(1):62
dc.identifier.urihttps://doi.org/10.1186/s13256-018-1959-6
dc.identifier.urihttps://doi.org/10.20381/ruor-23138
dc.identifier.urihttp://hdl.handle.net/10393/38886
dc.language.rfc3066en
dc.rights.holderThe Author(s).
dc.titleIdiopathic intracranial hypertension presenting as bilateral spontaneous lateral intrasphenoidal and transethmoidal meningoceles: a case report and review of the literature
dc.typeJournal Article

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