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Bilateral oculomotor ocular neuromyotonia: a case report

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 innervat...

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Autores principales: Padungkiatsagul, Tanyatuth, Jindahra, Panitha, Poonyathalang, Anuchit, Samipak, Narong, Vanikieti, Kavin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120096/
https://www.ncbi.nlm.nih.gov/pubmed/30176815
http://dx.doi.org/10.1186/s12883-018-1142-0
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author Padungkiatsagul, Tanyatuth
Jindahra, Panitha
Poonyathalang, Anuchit
Samipak, Narong
Vanikieti, Kavin
author_facet Padungkiatsagul, Tanyatuth
Jindahra, Panitha
Poonyathalang, Anuchit
Samipak, Narong
Vanikieti, Kavin
author_sort Padungkiatsagul, Tanyatuth
collection PubMed
description 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 2 min. 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12883-018-1142-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-61200962018-09-05 Bilateral oculomotor ocular neuromyotonia: a case report Padungkiatsagul, Tanyatuth Jindahra, Panitha Poonyathalang, Anuchit Samipak, Narong Vanikieti, Kavin BMC Neurol Case Report 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 2 min. 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12883-018-1142-0) contains supplementary material, which is available to authorized users. BioMed Central 2018-09-03 /pmc/articles/PMC6120096/ /pubmed/30176815 http://dx.doi.org/10.1186/s12883-018-1142-0 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Padungkiatsagul, Tanyatuth
Jindahra, Panitha
Poonyathalang, Anuchit
Samipak, Narong
Vanikieti, Kavin
Bilateral oculomotor ocular neuromyotonia: a case report
title Bilateral oculomotor ocular neuromyotonia: a case report
title_full Bilateral oculomotor ocular neuromyotonia: a case report
title_fullStr Bilateral oculomotor ocular neuromyotonia: a case report
title_full_unstemmed Bilateral oculomotor ocular neuromyotonia: a case report
title_short Bilateral oculomotor ocular neuromyotonia: a case report
title_sort bilateral oculomotor ocular neuromyotonia: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120096/
https://www.ncbi.nlm.nih.gov/pubmed/30176815
http://dx.doi.org/10.1186/s12883-018-1142-0
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