Department of Pediatric Neurology, Tacuarembó Regional Hospital, Tacuarembó, Uruguay.
Pediatr Neurol. 2011 Jan;44(1):61-4. doi: 10.1016/j.pediatrneurol.2010.08.018.
We report on a previously healthy 11-year-old boy with unilateral periorbital mild headache and facial nerve palsy, followed during the next 5 months by recurrent unilateral headaches and subsequent extrinsic paresis of the third cranial nerve and paresis of the sixth cranial nerve, each of which improved with steroids. Cranial magnetic resonance imaging revealed increased thickening of the left cavernous sinus and adjacent structures, with marked gadolinium enhancement. Eight months after the initial signs, he developed left retro-orbital headache that lasted 16 days and was relieved 24 hours after resuming steroid treatment. Recurrent multiple cranial neuropathies, neuroimaging findings, and long-lasting headache that responded to steroids indicated Tolosa-Hunt syndrome, further confirmed by extensive investigation and a long follow-up to exclude other causes. This patient illustrates the complexity of disorders with multiple cranial nerve palsies, and adds to the sparse literature on Tolosa-Hunt syndrome in children, describing the first pediatric case preceded by facial palsy.
我们报告了一例此前健康的 11 岁男孩,他出现单侧眶周轻度头痛和面神经瘫痪,随后在接下来的 5 个月中反复发作单侧头痛,随后第三颅神经和第六颅神经外展神经麻痹,这些症状均用类固醇治疗后改善。颅脑磁共振成像显示左侧海绵窦及邻近结构增厚,钆增强明显。初始症状出现 8 个月后,他出现左侧眼眶后头痛,持续 16 天,在恢复类固醇治疗 24 小时后缓解。复发性多发性颅神经病变、神经影像学发现以及对类固醇治疗有反应的长期头痛提示托洛萨-亨特综合征,通过广泛的调查和长期随访排除其他原因进一步证实了这一点。本例患者说明了具有多种颅神经麻痹的疾病的复杂性,并增加了关于儿童托洛萨-亨特综合征的文献,描述了首例面神经瘫痪前的儿科病例。