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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/36354
Title: Pediatric primary optic nerve sheath meningioma
Authors: Kavin Vanikieti
Pisit Preechawat
Anuchit Poonyathalang
Mahidol University
Keywords: Medicine
Issue Date: 4-Aug-2015
Citation: International Medical Case Reports Journal. Vol.8, (2015), 159-163
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.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84940049683&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/36354
ISSN: 1179142X
Appears in Collections:Scopus 2011-2015

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