Verrotti Alberto, Spartà Maria Valentina, Monacelli Debora, Porto Rossella, Castagnino Miriam, Russo Raucci Annalisa, Compagno Francesca, Viglio Simona, Foiadelli Thomas, Nicita Francesco, Grosso Salvatore, Spalice Alberto, Chiarelli Francesco, Marseglia Gianluigi, Savasta Salvatore
Department of Pediatrics, Perugia University, Perugia, Italy.
Epilepsia. 2014 Aug;55(8):1213-9. doi: 10.1111/epi.12699. Epub 2014 Jun 25.
Epilepsy in Ehlers-Danlos syndrome (EDS) has been reported in the literature, but there are no studies that have investigated in detail clinical and electroencephalography (EEG) features in patients with EDS, and that have compared the outcome of epilepsy in subjects with or without brain lesions. We report a series of 42 patients with EDS and epilepsy, including data that concern clinical characteristics, EEG abnormalities, brain malformations at magnetic resonance imaging (MRI) and long-term outcome.
EEG, clinical information, and neuroimaging characteristics in 42 patients with EDS were analyzed at the onset of epilepsy and after long-term follow-up (at least 5 years). We subdivided the patients into two groups: group A, 26 patients without brain abnormalities; group B, 16 patients with brain lesions, often with periventricular heterotopia (PH).
Group A patients: Most cases (19 of 26) presented focal epilepsy, whereas 7 of 26 were affected by generalized epilepsy; interictal EEG showed temporal or temporoparietal spikes in most cases. Twenty-three patients received antiepileptic drug (AED) monotherapy; three patients were treated with polytherapy. During follow-up, all patients were seizure-free for at least 2 years, and only one continued to receive AEDs. Group B patients: the majority presented focal epilepsy (9 of 16), but many patients had generalized epilepsy (7 of 16); interictal EEG showed usually frontal or frontotemporal spikes and waves. Many patients (12 of 16) received AED polytherapy. During follow-up, 12 patients were seizure-free, and all patients continued pharmacologic treatment.
All patients without brain lesions showed a favorable response to AED monotherapy and were seizure-free after a few years of treatment. Patients with central nervous system abnormalities had a worse outcome, suggesting that the presence of brain lesions could influence the long-term evolution in these patients.
文献中已有关于埃勒斯-当洛综合征(EDS)合并癫痫的报道,但尚无研究详细调查EDS患者的临床及脑电图(EEG)特征,也未比较有或无脑部病变的患者癫痫的预后情况。我们报告了42例EDS合并癫痫的患者系列,包括临床特征、EEG异常、磁共振成像(MRI)显示的脑畸形及长期预后的数据。
对42例EDS合并癫痫患者在癫痫发作时及长期随访(至少5年)后进行EEG、临床信息及神经影像学特征分析。我们将患者分为两组:A组,26例无脑部异常的患者;B组,16例有脑部病变的患者,常伴有脑室周围异位(PH)。
A组患者:大多数病例(26例中的19例)表现为局灶性癫痫,而26例中的7例为全身性癫痫;发作间期EEG在大多数情况下显示颞叶或颞顶叶棘波。23例患者接受抗癫痫药物(AED)单药治疗;3例患者接受联合治疗。随访期间,所有患者至少2年无癫痫发作,只有1例继续接受AED治疗。B组患者:大多数表现为局灶性癫痫(16例中的9例),但许多患者为全身性癫痫(16例中的7例);发作间期EEG通常显示额叶或额颞叶棘波和慢波。许多患者(16例中的12例)接受AED联合治疗。随访期间,12例患者无癫痫发作,所有患者继续药物治疗。
所有无脑部病变的患者对AED单药治疗反应良好,治疗几年后无癫痫发作。中枢神经系统异常的患者预后较差,提示脑部病变的存在可能影响这些患者的长期病情演变。