Publication:
Bilateral oculomotor ocular neuromyotonia: A case report

dc.contributor.authorTanyatuth Padungkiatsagulen_US
dc.contributor.authorPanitha Jindahraen_US
dc.contributor.authorAnuchit Poonyathalangen_US
dc.contributor.authorNarong Samipaken_US
dc.contributor.authorKavin Vanikietien_US
dc.contributor.otherFaculty of Medicine, Ramathibodi Hospital, Mahidol Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2019-08-23T11:44:15Z
dc.date.available2019-08-23T11:44:15Z
dc.date.issued2018-09-03en_US
dc.description.abstract© 2018 The Author(s). Background: Ocular neuromyotonia (ONM) is characterized by episodic diplopia, which is usually triggered by prolonged eccentric gaze of the affected extraocular muscles. The spell is characterized by involuntary, occasionally painful, sustained contraction of one or more extraocular muscles innervated by the oculomotor, trochlear, or abducens nerve. ONM usually occurs as a late consequence of radiotherapy around the parasellar area, although idiopathic cases have been reported. Most cases are unilateral; however, bilateral ONM has occasionally been described. Case presentation: A 60-year-old woman presented with a 4-month history of episodic, painful, horizontal binocular diplopia. She underwent external beam radiotherapy to the skull base for treatment of nasopharyngeal carcinoma. The tumor was well controlled. General neurological examination findings were unremarkable. Neuro-ophthalmic examination revealed normal visual acuity, visual fields, pupils, and fundi. Ocular alignment showed orthotropia with normal ocular motility. Myasthenic eyelid signs were absent. However, she developed episodes of involuntary sustained contraction of the medial rectus muscle following prolonged eccentric gaze toward the affected medial rectus muscle, which resulted in esotropia upon returning to the primary position. The esotropic episodes spontaneously resolved after approximately 2min. These spells affected both medial rectus muscles. Both pupils remained normal throughout the examination. Magnetic resonance imaging revealed neither brain parenchyma/brain stem lesions nor tumor recurrence. Her symptoms were successfully treated with carbamazepine. Conclusions: Episodic esotropia in the adducting eye following prolonged horizontal eccentric gaze is a significant characteristic of ONM affecting the bilateral medial rectus muscles (i.e., bilateral oculomotor ONM). In spite of its extreme rarity, ONM should be considered as a differential diagnosis of episodic diplopia, especially in patients with a history of radiotherapy around the parasellar area. Careful examination with prolonged eccentric gaze should be performed to achieve a correct diagnosis and avoid an extensive unnecessary workup.en_US
dc.identifier.citationBMC Neurology. Vol.18, No.1 (2018)en_US
dc.identifier.doi10.1186/s12883-018-1142-0en_US
dc.identifier.issn14712377en_US
dc.identifier.other2-s2.0-85052714359en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/46331
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85052714359&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleBilateral oculomotor ocular neuromyotonia: A case reporten_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85052714359&origin=inwarden_US

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