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From the Neurology Department, Hospital Privado de Comunidad, Mar del Plata, Argentina.
Address correspondence and reprint requests to Dr. Lucas Martín Romano, Córdoba 4545, Neurology Department, Hospital Privado de Comunidad, Mar del Plata, ZC 7600, Argentina lromano{at}sna.org.ar
A 13-year-old girl presented with left-sided periorbital headache and homolateral ptosis with normal ocular motility and pupillary response (video segment 1 on the Neurology® Web site at www.neurology.org). She had a similar episode 1 year before. Brain MRI showed enhancement of the left oculomotor nerve (figure). She recovered completely within 7 days (video segment 2). Two months later, MRI was normal.
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Ophthalmoplegic migraine is very rare. One similar report was identified in the literature.1
Differential diagnoses include neoplasm, aneurysm, carotid dissection, temporal arteritis, sarcoidosis, Tolosa-Hunt syndrome, and infectious etiologies.
Response to steroids and the reversible MRI contrast enhancement of the affected cranial nerve both point to an inflammatory mechanism rather than a migrainous condition, and introduce the possibility of reclassifying ophthalmoplegic migraine as a recurrent neuritis.2
Supplemental data at www.neurology.org
Disclosure: The authors report no disclosures.
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