Otani K, Tagawa T, Futagi Y, Okamoto N, Yabuuchi H
Division of Pediatric Neurology, Osaka Medical Center, Research Institute for Maternal and Child Health, Japan.
Brain Dev. 1991 May;13(3):196-9. doi: 10.1016/s0387-7604(12)80031-3.
Induced microseizures (IMS) were observed in a 5-month-old girl with symptomatic West syndrome. The seizures occurred following the suppression of infantile spasms with adrenocorticotropic hormone therapy and disappeared following the cessation of clonazepam administration. The ictal manifestations consisted of periods of irregular respiration, and respiratory arrest lasting for several seconds which often involved opening of the eyes and mild extension of the neck corresponding with the diffuse fast wave bursts in EEG activity observed during sleep. These seizures were thought to be equivalent to the IMS in Lennox-Gastaut syndrome, which have never been reported before in patients with West syndrome.
在一名患有症状性韦斯特综合征的5个月大女孩中观察到诱发性微发作(IMS)。这些发作在促肾上腺皮质激素治疗抑制婴儿痉挛后出现,并在停用氯硝西泮后消失。发作期表现为呼吸不规则,呼吸暂停持续数秒,常伴有睁眼和颈部轻度伸展,与睡眠期间脑电图活动中观察到的弥漫性快波爆发相对应。这些发作被认为等同于 Lennox-Gastaut 综合征中的 IMS,此前在韦斯特综合征患者中从未有过报道。