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dc.contributor.authorKaynar, MY
dc.contributor.authorCiplak, N
dc.contributor.authorBozkus, H
dc.contributor.authorErdincler, P
dc.date.accessioned2021-03-06T09:02:52Z
dc.date.available2021-03-06T09:02:52Z
dc.date.issued1999
dc.identifier.citationErdincler P., Kaynar M., Bozkus H., Ciplak N., "Posterior fossa arachnoid cysts", BRITISH JOURNAL OF NEUROSURGERY, cilt.13, ss.10-17, 1999
dc.identifier.issn0268-8697
dc.identifier.otherav_e3e56ea1-d6fb-45c7-9fc5-edb686677274
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/149941
dc.identifier.urihttps://doi.org/10.1080/02688699944122
dc.description.abstractArachnoid cysts of the posterior fossa are rare lesions that are considered to be mostly congenital in origin. In this article, we retrospectively review 12 patients who underwent surgical treatment for their symptomatic posterior fossa arachnoid cysts. The most common presenting symptoms were gait disturbances and headache. The diagnosis was established on computed tomography or magnetic resonance imaging. Surgery consisted of cyst wall excision with fenestration in nine cases and shunting procedures in three cases. In all cases except one who died, the postsurgical follow-up neuroradiological investigations showed that the cysts had decreased in size, the cerebellum had re-expanded, and if there was preoperative hydrocephalus, the ventricular size was decreased. The follow-up period ranged from 1 to 11 years. All surviving cases are free of symptoms and no arachnoid cysts recurred. The classification, pathophysiology; differential diagnosis and surgical treatment of infratentorial arachnoid cysts are discussed and the relevant literature is reviewed.
dc.language.isoeng
dc.subjectCerrahi Tıp Bilimleri
dc.subjectTıp
dc.subjectNöroloji
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectCERRAHİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titlePosterior fossa arachnoid cysts
dc.typeMakale
dc.relation.journalBRITISH JOURNAL OF NEUROSURGERY
dc.contributor.department, ,
dc.identifier.volume13
dc.identifier.issue1
dc.identifier.startpage10
dc.identifier.endpage17
dc.contributor.firstauthorID122666


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