Pareja Juan A, Caminero Ana B, Sjaastad Ottar
Department of Neurology, Hospital Ruber Internacional, Madrid, Spain.
CNS Drugs. 2002;16(6):373-83. doi: 10.2165/00023210-200216060-00002.
Short-lasting Unilateral Neuralgiform headache attacks with Conjunctival injection and Tearing (SUNCT) is a syndrome predominant in males, with a mean age of onset around 50 years. The attacks are strictly unilateral, generally with the pain persistently confined to the ocular/periocular area. Most attacks are moderate to severe in intensity and burning, stabbing or electrical in character. The mean duration of paroxysms is 1 minute, with a usual range of 10 to 120 seconds (total range 5 to 250 seconds). Prominent, ipsilateral conjunctival injection and lacrimation regularly accompany the attacks. Nasal stuffiness/rhinorrhoea are frequently noted. In addition, there is subclinical forehead sweating. During attacks, there is increased intraocular pressure on the symptomatic side and swelling of the eyelids. No changes in pupil diameter have been observed. Attacks can be triggered mostly from trigeminally innervated areas, but also from the extratrigeminal territory. There are also spontaneous attacks. An irregular temporal pattern is the rule, with symptomatic periods alternating with remissions in an unpredictable fashion. During active periods, the frequency of attacks may vary from <1 attack/day to >30 attacks/hour. The attacks predominate during the daytime, nocturnal attacks being seldom reported. A SUNCT-like picture has been described in some patients with either intra-axial or extra-axial posterior fossa lesions, mostly vascular disturbances/ malformations. In the vast majority of patients, however, aetiology and pathogenesis are unknown. In SUNCT syndrome, there is a lack of persistent, convincingly beneficial effect of drugs or anaesthetic blockades that are generally effective in cluster headache, chronic paroxysmal hemicrania, trigeminal neuralgia, idiopathic stabbing headache ('jabs and jolts syndrome'), and other headaches more faintly resembling SUNCT syndrome. Single reports have claimed that carbamazepine, lamotrigine, gabapentin, corticosteroids or surgical procedures may be of help. However, caution is recommended when assessing any therapy in a disorder such as SUNCT syndrome, in which the rather chaotic and unpredictable temporal pattern makes the assessment of any drug/therapeutic effect per se a particularly difficult matter.
伴有结膜充血和流泪的短暂性单侧神经痛样头痛发作(SUNCT)是一种以男性为主的综合征,平均发病年龄约为50岁。发作严格单侧,疼痛通常持续局限于眼部/眼周区域。大多数发作强度为中度至重度,性质为烧灼样、刺痛样或电击样。发作的平均持续时间为1分钟,通常范围为10至120秒(总范围为5至250秒)。发作时常伴有明显的同侧结膜充血和流泪。常伴有鼻塞/流涕。此外,存在亚临床的前额出汗。发作期间,患侧眼压升高,眼睑肿胀。未观察到瞳孔直径变化。发作大多可由三叉神经支配区域触发,但也可由三叉神经外区域触发。也有自发发作。发作时间模式不规则,症状期与缓解期以不可预测的方式交替。在活动期,发作频率可从每天少于1次发作到每小时超过30次发作不等。发作多在白天,很少有夜间发作的报道。在一些患有轴内或轴外后颅窝病变(大多为血管紊乱/畸形)的患者中,曾描述过类似SUNCT的表现。然而,绝大多数患者的病因和发病机制尚不清楚。在SUNCT综合征中,药物或麻醉阻滞通常对丛集性头痛、慢性阵发性偏侧头痛、三叉神经痛、特发性刺痛性头痛(“刺痛和电击综合征”)以及其他与SUNCT综合征相似性较低的头痛有效,但在SUNCT综合征中却缺乏持续、令人信服的有益效果。有个别报道称卡马西平、拉莫三嗪、加巴喷丁、皮质类固醇或手术可能有帮助。然而,在评估SUNCT综合征等疾病的任何治疗方法时应谨慎,因为其发作时间模式相当紊乱且不可预测,这使得评估任何药物/治疗效果本身成为一件特别困难的事情。