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儿童无头痛性偏头痛。

Acephalgic migraines of childhood.

作者信息

Shevell M I

机构信息

Department of Neurology/Neurosurgery, McGill University, Montreal, Quebec, Canada.

出版信息

Pediatr Neurol. 1996 Apr;14(3):211-5. doi: 10.1016/0887-8994(96)00019-7.

Abstract

Migraine aura without headache (acephalgic migraines) is a recognized subset of migrainous phenomena in the adult population. No reports of its prevalence or characteristics in a series of children exists. Using diagnostic criteria for migraine aura without headache established by the International Headache Society, a retrospective review of a computerized database of all patients referred over a 4-year period (July 1991 to June 1995 inclusive) to a single university-based pediatric neurologist was performed. Fourteen patients were identified, representing 2% of all patients with a primary diagnosis of migraine. Nine were females and 13 had a strong family history of migraines. Age of onset of symptoms ranged from 5 to 12 years with a mean of 8 years. Symptoms were episodic in all, varying in frequency from weekly to more typically monthly, lasting generally less than 10 min. In 9 patients the aura described was that of often colorful photopsias or scintillating scotomas. Two had micropsia, one had temporal distortion (time "speeded up"), one had hyperacusis, and the final patient had a vague sense of disconnection from her surroundings. Only 2 patients had a headache occasionally associated with the described aura. In addition to the acephalgic migraines, 9 patients had either common or classical migraines, the latter typically featuring aura distinct from those observed in these patients' acephalgic episodes. Neurologic examination, electrophysiologic investigation (EEG/evoked potentials), and neuroimaging were noncontributory in all instances. Migraine aura without headache is a recognizable benign migraine syndrome of late childhood.

摘要

无头痛性偏头痛先兆是成人偏头痛现象中已被认可的一个子集。目前尚无关于其在一系列儿童中的患病率或特征的报道。采用国际头痛协会制定的无头痛性偏头痛先兆的诊断标准,对一位大学儿科神经科医生在4年期间(1991年7月至1995年6月,含起止时间)接诊的所有患者的计算机化数据库进行了回顾性分析。共识别出14例患者,占所有初步诊断为偏头痛患者的2%。其中9例为女性,13例有偏头痛家族史。症状出现的年龄在5至12岁之间,平均为8岁。所有患者症状均为发作性,发作频率从每周一次到更常见的每月一次不等,通常持续时间少于10分钟。9例患者描述的先兆为常有彩色光幻视或闪烁暗点。2例有视物显小症,1例有颞部变形(时间“加速”),1例有听觉过敏,最后1例患者有一种与周围环境的模糊脱离感。只有2例患者偶尔会出现与所述先兆相关的头痛。除了无头痛性偏头痛,9例患者还患有普通偏头痛或典型偏头痛,后者的典型特征是先兆与这些患者无头痛发作时观察到的先兆不同。在所有病例中,神经学检查、电生理检查(脑电图/诱发电位)和神经影像学检查均无异常发现。无头痛性偏头痛先兆是儿童晚期一种可识别的良性偏头痛综合征。

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