Literature DB >> 26071177

[Oculomotor nerve schwannoma in a child: Case report and literature review].

A Jibia1, L Chenin2, M Lefranc2, J Peltier2.   

Abstract

An isolated schwannoma of the oculomotor nerve is rare in children without an associated neurofibromatosis. A 13-year-old girl, with a previous medical history of migraine, was admitted for disabling ophthalmic migraine with oblique diplopia. The clinical examination showed a right incomplete ophthalmoplegia with reduced ipsilateral visual acuity (8/10). There was no particular skin reaction. The MRI revealed a right (isosignal-T1 and isosignal-T2) nodular schwannoma located within the cisternal segment of the oculomotor nerve. The angio-CT performed later confirmed the absence of any vascular malformation. The treatment consisted of analgesics and corticotherapy, with complete regression of symptoms three weeks later and a normal MRI follow-up. Therefore, radiosurgery was not performed.
Copyright © 2015 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Childhood; Corticotherapy; Corticothérapie; Nerf oculomoteur; Oculomotor nerve; Pédiatrie; Schwannoma; Schwannome

Mesh:

Year:  2015        PMID: 26071177     DOI: 10.1016/j.neuchi.2015.03.007

Source DB:  PubMed          Journal:  Neurochirurgie        ISSN: 0028-3770            Impact factor:   1.553


  2 in total

1.  Recurrent painful ophthalmoplegic neuropathy revealing oculomotor nerve schwannoma.

Authors:  Saloua Mrabet; Amina Nasri; Nahed Kessentini; Mouna Ben Djebara; Amina Gargouri-Berrechid; Imen Kacem; Riadh Gouider
Journal:  Tunis Med       Date:  2021 Aout

Review 2.  Recurrent Painful Ophthalmoplegic Neuropathy and Oculomotor Nerve Schwannoma: A Pediatric Case Report with Long-Term MRI Follow-Up and Literature Review.

Authors:  Maria Giuseppina Petruzzelli; Mariella Margari; Flora Furente; Maria Carmela Costanza; Anna Rosi Legrottaglie; Franca Dicuonzo; Lucia Margari
Journal:  Pain Res Manag       Date:  2019-09-25       Impact factor: 3.037

  2 in total

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