Publication:
Pediatric primary optic nerve sheath meningioma

dc.contributor.authorKavin Vanikietien_US
dc.contributor.authorPisit Preechawaten_US
dc.contributor.authorAnuchit Poonyathalangen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-11-23T10:38:44Z
dc.date.available2018-11-23T10:38:44Z
dc.date.issued2015-08-04en_US
dc.description.abstract© 2015 Vanikieti et al. Primary optic nerve sheath meningioma (PONSM) is extremely rare among children. We report two cases of pediatric PONSM. The first case was a 12-year-old boy who presented with gradual visual loss of his right eye and was found to be associated with neurofibromatosis type 2. The second case was a 10-year-old boy who presented with gradual proptosis of his left eye with normal visual acuity. Severe visual loss is a common clinical manifestation of pediatric PONSM. Although the visual acuity in the second case was normal, his vision rapidly deteriorated to 20/200. In both cases, the diagnosis of PONSM was confirmed by magnetic resonance imaging, and a successful tumor growth control was achieved after stereotactic radiotherapy was implemented.en_US
dc.identifier.citationInternational Medical Case Reports Journal. Vol.8, (2015), 159-163en_US
dc.identifier.doi10.2147/IMCRJ.S82795en_US
dc.identifier.issn1179142Xen_US
dc.identifier.other2-s2.0-84940049683en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/36354
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84940049683&origin=inwarden_US
dc.subjectMedicineen_US
dc.titlePediatric primary optic nerve sheath meningiomaen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84940049683&origin=inwarden_US

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