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Bilateral oculomotor ocular neuromyotonia: a case report.
Padungkiatsagul, Tanyatuth; Jindahra, Panitha; Poonyathalang, Anuchit; Samipak, Narong; Vanikieti, Kavin.
Afiliação
  • Padungkiatsagul T; Department of Ophthalmology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, 270 Rama VI Road, Bangkok, 10400, Thailand.
  • Jindahra P; Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, 270 Rama VI Road, Bangkok, 10400, Thailand.
  • Poonyathalang A; Department of Ophthalmology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, 270 Rama VI Road, Bangkok, 10400, Thailand.
  • Samipak N; Chakri Nareubodindra Medical Institute, Faculty of Medicine Ramathibodi Hospital, Mahidol University, National Highway 1011, Bang Phli district, Samutprakarn, 10540, Thailand.
  • Vanikieti K; Department of Ophthalmology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, 270 Rama VI Road, Bangkok, 10400, Thailand. Vanikieti.kavin@gmail.com.
BMC Neurol ; 18(1): 137, 2018 Sep 03.
Article em En | MEDLINE | ID: mdl-30176815
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Lesões por Radiação / Síndrome de Isaacs Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Middle aged Idioma: En Revista: BMC Neurol Assunto da revista: NEUROLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Tailândia

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Lesões por Radiação / Síndrome de Isaacs Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Middle aged Idioma: En Revista: BMC Neurol Assunto da revista: NEUROLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Tailândia