| Literature DB >> 28512503 |
Laura Donaldson1, Ryan Rebello2, Amadeo Rodriguez1,2,3.
Abstract
A 45-year-old man presented with a slowly progressive pupil-involving third nerve palsy. Magnetic resonance imaging (MRI) revealed a tubular lesion extending from the interpeduncular cistern through the cavernous sinus and into the left orbit where it branched into a superior and an inferior division, clearly outlining the anatomy of the third cranial nerve. Multiple other, less pronounced, enlarged cranial nerves were noted. The differential diagnosis included chronic inflammatory demyelinating polyneuropathy (CIDP), hereditary motor and sensory neuropathy (HMSN), neurofibromatosis (NF), and schwannomatosis. The absence of other muscle weakness and of sensory symptoms combined with normal peripheral nerve conduction studies effectively ruled out the hypertrophic polyneuropathies and pointed to a syndromic cause of multiple benign peripheral nerve sheath tumours (PNSTs). The authors are treating this case as presumed schwannomatosis, a syndrome similar to NF2 with much lower frequency of acoustic neuromas.Entities:
Keywords: MRI; Oculomotor nerve; schwannomatosis
Year: 2017 PMID: 28512503 PMCID: PMC5417081 DOI: 10.1080/01658107.2017.1285319
Source DB: PubMed Journal: Neuroophthalmology ISSN: 0165-8107