Reflex Seizures as Initial Manifestations of Systemic Lupus Erythematosus in Childhood

Reflex Seizures as Initial Manifestations of Systemic Lupus Erythematosus in Childhood
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DOI:
10.1177/096120339300200118
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发表时间:
1993-02
期刊:
影响因子:
2.6
通讯作者:
M. Brinciotti;G. Ferrucci;G. Trasatti;R. Priori;E. Squilloni;G. Valesini
M. Brinciotti;G. Ferrucci;G. Trasatti;R. Priori;E. Squilloni;G. Valesini
中科院分区:
医学4区
文献类型:
--
作者:
M. Brinciotti;G. Ferrucci;G. Trasatti;R. Priori;E. Squilloni;G. Valesini

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我们报告一位十岁女童,因视觉及听觉刺激而出现以幻视及幻听为特征的反射性癫痫发作。EEG显示左侧颞枕区的非典型棘波放电,明显激活的视觉和听觉刺激(间歇性光,模式反转刺激和单耳右纯音)。患者接受卡马西平治疗,癫痫发作在7个月内停止。从治疗开始10个月后,她出现了系统性红斑狼疮的体征。
We report a 10-year-old girl with reflex seizures characterized by visual and acoustic hallucinations, induced by visual and acoustic stimulations. The EEG showed atypical spike-wave discharges on the left temporo-occipital area, markedly activated by visual and acoustic stimuli (intermittent light, pattern-reversal stimulation and monoaural right pure tone). The patient was treated with carbamazepine and seizure stopped within 7 months. After 10 months from the start of the therapy she developed signs of systemic lupus erythematosus.