Wong V, Wong W C
Department of Pediatrics, The University of Hong Kong, Queen Mary Hospital.
Pediatr Neurol. 1997 Jul;17(1):70-3. doi: 10.1016/s0887-8994(97)80671-6.
The oculomotor nerve of a 6-year-old boy with recurrent headache and recurrent ophthalmoplegia was contrast-enhanced on a magnetic resonance imaging (MRI) scan during an episode. The boy exhibited dramatic response to steroid treatment. The clinical features of ophthalmoplegic migraine and Tolosa-Hunt syndrome overlapped in this patient. We suggest that a positive MRI finding can be included as one of the diagnostic criteria in the classification of ophthalmoplegic migraine and that a trial of steroid is worthwhile in the presence of enhancement of the oculomotor nerve since ophthalmoplegic migraine may be noninfectious but inflammatory in etiology.
一名患有复发性头痛和复发性眼肌麻痹的6岁男孩,在一次发作期间进行的磁共振成像(MRI)扫描显示其动眼神经有强化表现。该男孩对类固醇治疗有显著反应。此患者的眼肌麻痹性偏头痛和托洛萨-亨特综合征的临床特征相互重叠。我们建议,MRI检查阳性结果可纳入眼肌麻痹性偏头痛分类的诊断标准之一,并且在动眼神经出现强化表现时,进行类固醇试验是值得的,因为眼肌麻痹性偏头痛病因可能是非感染性的,而是炎症性的。