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一例对佐米曲坦反应敏感的丛集性头痛综合征。

A case of SUNCT syndrome responsive to zonisamide.

机构信息

Shizuoka-Shimizu Municipal Hospital, Japan.

出版信息

Cephalalgia. 2011 Mar;31(4):501-3. doi: 10.1177/0333102410387680. Epub 2010 Oct 29.

Abstract

Short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing (SUNCT) is a rare headache syndrome that represents a subtype of trigeminal autonomic cephalalgia thought to be highly refractory to treatment. More recently, numerous anticonvulsant agents including lamotrigine, topiramate, gabapentin, and carbamazepine have been reported to be partially or completely effective for treating SUNCT. We report the case of a patient with SUNCT in whom symptoms were completely relieved with carbamazepine at 600 mg/day. However, carbamazepine had to be discontinued due to severe rash. Zonisamide was selected for continued treatment, as a Na-channel blocker like carbamazepine but with lower risk of producing skin rashes as caused by carbamazepine. Attacks ceased completely with 300 mg/day of zonisamide achieving a blood serum level of 19 µg/ml. This is the first case report to describe zonisamide alone completely eliminating SUNCT symptoms. Zonisamide should be considered a viable candidate drug for the treatment of SUNCT.

摘要

短暂单侧神经痛样头痛发作伴结膜充血和流泪(SUNCT)是一种罕见的头痛综合征,属于三叉神经自主神经性头痛的一个亚型,被认为对治疗具有高度抗性。最近,许多抗惊厥药物,包括拉莫三嗪、托吡酯、加巴喷丁和卡马西平,已被报道对治疗 SUNCT 具有部分或完全疗效。我们报告了一例 SUNCT 患者,其症状在卡马西平 600mg/天的治疗下完全缓解。然而,由于严重皮疹,卡马西平不得不停药。由于佐尼沙胺是一种与卡马西平相似的钠离子通道阻滞剂,但引起皮疹的风险较低,因此选择佐尼沙胺继续治疗。每天 300mg 的佐尼沙胺使血清水平达到 19µg/ml,使发作完全停止。这是首例单独使用佐尼沙胺完全消除 SUNCT 症状的病例报告。佐尼沙胺应被视为治疗 SUNCT 的一种可行候选药物。

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