Literature DB >> 22295922

Pediatric orbital schwannoma originating from the oculomotor nerve.

Hiroaki Nagashima1, Kazuki Yamamoto, Atsufumi Kawamura, Tatsuya Nagashima, Koji Nomura, Makiko Yoshida.   

Abstract

Intraorbital schwannoma is a rare tumor that constitutes approximately 1%-8% of all orbital tumors. The authors report a case of orbital schwannoma in a 5-year-old boy who was admitted to their institute with exophthalmos and ptosis of the right eye. Computed tomography scanning and MR imaging revealed a retroocular mass in the right orbit. The tumor was successfully removed via a transcranial approach. The pathological diagnosis was schwannoma that appeared to originate from the superior branch of the oculomotor nerve. Despite the rarity of these intraorbital extraocular tumors in children, schwannomas should be differentiated from other intraorbital tumors.

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Year:  2012        PMID: 22295922     DOI: 10.3171/2011.11.PEDS1192

Source DB:  PubMed          Journal:  J Neurosurg Pediatr        ISSN: 1933-0707            Impact factor:   2.375


  3 in total

1.  Clinicopathological features of peripheral nerve sheath tumors involving the eye and ocular adnexa.

Authors:  Mingjuan L Zhang; Maria J Suarez; Thomas M Bosley; Fausto J Rodriguez
Journal:  Hum Pathol       Date:  2017-02-22       Impact factor: 3.466

2.  Recurrent orbital schwannomas: clinical course and histopathologic correlation.

Authors:  Michelle Kron; Brenda L Bohnsack; Steven M Archer; Jonathan B McHugh; Alon Kahana
Journal:  BMC Ophthalmol       Date:  2012-08-31       Impact factor: 2.209

3.  Pure Intra-optic Canal Schwannoma: Report of Two Cases.

Authors:  Sayuru Miyamura; Satoshi Yamaguchi; Masaaki Takeda; Takafumi Mitsuhara; Masahiro Hosogai; Kazuhiko Sugiyama; Kaoru Kurisu
Journal:  Asian J Neurosurg       Date:  2017 Oct-Dec
  3 in total

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