Publication: Pediatric primary optic nerve sheath meningioma
dc.contributor.author | Kavin Vanikieti | en_US |
dc.contributor.author | Pisit Preechawat | en_US |
dc.contributor.author | Anuchit Poonyathalang | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.date.accessioned | 2018-11-23T10:38:44Z | |
dc.date.available | 2018-11-23T10:38:44Z | |
dc.date.issued | 2015-08-04 | en_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.citation | International Medical Case Reports Journal. Vol.8, (2015), 159-163 | en_US |
dc.identifier.doi | 10.2147/IMCRJ.S82795 | en_US |
dc.identifier.issn | 1179142X | en_US |
dc.identifier.other | 2-s2.0-84940049683 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/36354 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84940049683&origin=inward | en_US |
dc.subject | Medicine | en_US |
dc.title | Pediatric primary optic nerve sheath meningioma | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84940049683&origin=inward | en_US |