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热性感染相关性癫痫综合征后出现惊吓诱发发作的成人起病癫痫:一例报告

Adult-onset epilepsy with startle-induced seizure after febrile infection-related epilepsy syndrome: A case report.

作者信息

Konomatsu Kazutoshi, Kakisaka Yosuke, Jin Kazutaka, Fujiwara Yu, Kubota Takafumi, Ogawa Maimi, Ishida Makoto, Ukishiro Kazushi, Ono Hirohiko, Kaneko Kimihiko, Sugeno Naoto, Aoki Masashi, Nakasato Nobukazu

机构信息

Department of Epileptology, Tohoku University Graduate School of Medicine, Sendai, Miyagi, Japan.

Department of Neurology, Tohoku University Graduate School of Medicine, Sendai, Miyagi, Japan.

出版信息

Epileptic Disord. 2025 Jun;27(3):451-456. doi: 10.1002/epd2.70026. Epub 2025 Apr 15.

Abstract

Startle-induced seizure is a rare type of reflex seizure triggered by unexpected sensory stimuli that often occurs in children with early acquired cerebral lesions or brain malformations. We report a unique case of adult-onset epilepsy with startle-induced seizures. A 24-year-old woman had suffered high fever and focal to bilateral tonic-clonic seizures. A diagnosis of febrile infection-related epilepsy syndrome (FIRES) was made based on the febrile infection occurring 7 days to 24 h before the onset of status epilepticus, which met all criteria for cryptogenic new-onset refractory status epilepticus (NORSE) according to the cryptogenic NORSE score. Immunotherapy and several antiseizure medications resulted in transient resolution of the seizures. Four months later, she experienced startle-induced seizures triggered by unexpected stimuli, such as auditory, visual, or unexpected events, and manifesting as initial tachycardia followed by right ear deafness, right hemifacial dysesthesia, eye deviation to the right, and tonic-clonic convulsions. Ictal electroencephalography revealed left temporal initial rhythmic delta activity, followed by rhythmic theta activity. The patient was diagnosed with startle epilepsy associated with FIRES and continued to receive anti-seizure medications. Claustrum-insular-operculum lesions may have been the epileptic focus in this case, in contrast to previous cases of epilepsy with startle-induced seizures originating in a frontoparietal network. This case indicates a new category of adult-onset post-FIRES epilepsy with startle-induced seizures.

摘要

惊吓诱发癫痫发作是一种罕见的反射性癫痫发作类型,由意外的感觉刺激触发,常见于早期获得性脑损伤或脑畸形的儿童。我们报告一例成人起病的伴有惊吓诱发癫痫发作的癫痫病例。一名24岁女性曾患高热及局灶性至双侧强直阵挛发作。根据癫痫持续状态发作前7天至24小时发生的发热感染,诊断为发热感染相关癫痫综合征(FIRES),根据隐源性新发性难治性癫痫持续状态(NORSE)评分,该病例符合所有隐源性NORSE标准。免疫治疗和几种抗癫痫药物使癫痫发作暂时缓解。四个月后,她经历了由意外刺激引发的惊吓诱发癫痫发作,如听觉、视觉或意外事件,表现为最初的心动过速,随后是右耳聋、右侧面部感觉异常、眼球向右偏斜和强直阵挛性惊厥。发作期脑电图显示左侧颞叶起始的节律性δ活动,随后是节律性θ活动。该患者被诊断为与FIRES相关的惊吓癫痫,并继续接受抗癫痫药物治疗。与之前起源于额顶叶网络的惊吓诱发癫痫发作的病例不同,岛叶-岛盖部病变可能是该病例的癫痫病灶。该病例表明了一种新的成人起病的FIRES后伴有惊吓诱发癫痫发作的癫痫类型。

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