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[A pediatric case of ophthalmoplegic migraine with recurrent oculomotor nerve palsy]
H Ishikawa1, M Yoshihara, K Mizuki
1Department of Ophthalmology, Nihon University School of Medicine, Tokyo, Japan.
Insights
Ophthalmoplegic migraine can cause recurrent oculomotor nerve palsy in children. Timolol maleate eye drops effectively reduced migraine frequency and symptoms in a young patient.
Area of Science:
- Neurology
- Ophthalmology
Background:
- Ophthalmoplegic migraine is a rare disorder characterized by recurrent cranial nerve palsies, most commonly affecting the oculomotor nerve.
- Diagnosis can be challenging, especially in young children, due to overlapping symptoms with other neurological conditions.
Observation:
- A 4-year-old girl presented with recurrent episodes of left ptosis and double vision, accompanied by drowsiness and vomiting.
- Clinical examination revealed left oculomotor nerve palsy with internal ophthalmoplegia, which resolved spontaneously.
- Neuroimaging and electroencephalography showed no significant abnormalities.
Findings:
- The patient experienced two further episodes of isolated oculomotor nerve palsy and mydriasis.
- Topical timolol maleate (0.25% twice daily) significantly reduced the frequency and severity of migraine attacks and associated symptoms.
- This suggests a potential therapeutic role for beta-blockers in managing ophthalmoplegic migraine.
Implications:
- Ophthalmoplegic migraine should be considered in the differential diagnosis of isolated oculomotor nerve palsy in childhood.
- A thorough case history focusing on recurrent migraine symptoms is crucial for accurate diagnosis.
- This case highlights the importance of considering migraine as a cause of recurrent cranial nerve palsies in pediatric patients.
Purpose:
A young patient of ophthalmoplegic migraine with recurrent oculomotor nerve palsy is reported.
Case:
A 4-year-old girl came to our hospital complaining of recurrent left ptosis and double vision which completely resolved within a few days. She had a history of drowsiness after vomiting every two months. Left oculomotor nerve palsy with internal ophthalmoplegia was observed. Electroencephalography revealed mild changes, but computed tomography, single photon emission computed tomography, and cerebrovascular Doppler-ultrasound examination demonstrated no abnormalities. This oculomotor nerve palsy completely improved on the next day.
Results:
Thereafter, left episodic mydriasis and oculomotor nerve palsy occurred twice each. However, the frequency and symptoms of migraine were remarkably reduced by topical administration of 0.25% timolol maleate twice daily to both eyes.
Conclusion:
In isolated oculomotor nerve palsy in childhood, ophthalmoplegic migraine should be also considered. We emphasize that a detailed case history is very important to its diagnosis.
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