Gaggero Roberto, Pistorio Angela, Pignatelli Sara, Rossi Alessandra, Mancardi Maria Margherita, Baglietto Maria Giuseppina, Striano Pasquale, Verrotti Alberto
Pediatric Unit, San Paolo Hospital, Savona, Italy.
Servizio Epidemiologia e Biostatistica, Italy.
Eur J Paediatr Neurol. 2014 May;18(3):376-80. doi: 10.1016/j.ejpn.2014.01.011. Epub 2014 Feb 16.
To evaluate the possibility of early syndrome classification of idiopathic partial epilepsies in children at the first seizure.
In this observational study we prospectively evaluated 298 patients, aged between 1 month and 17 years and consecutively referred for the first unprovoked focal seizure. The whole cohort included 133 patients; the final analysis was carried out on 107 (59 males) individuals. Age at the first seizure ranged between 2.3 and 13.0 years. Clinical and EEG data of all patients were independently reviewed by two medical doctors. Patients were followed-up for at least 5 years, with a mean period of follow-up of 6.9 years.
After the first seizure, a specific syndrome could be diagnosed in eighty (74.7%) children. In particular, Childhood Epilepsy with Centro-Temporal Spikes (CECTS) 42.9% of cases, Panayiotopoulos Syndrome (PS) 28.9%, idiopathic childhood occipital epilepsy of Gastaut (ICOE-G) 2.8%. Unclassified cases were 25.4%. At the end of the follow-up, the diagnosis was confirmed in 72 of 80 children (90%): BCECTS 89% of patients, PS 90% and ICOE-G 100%: among the unclassified cases, in 11 patients (40.7%) the diagnosis did not change, whereas 16 patients (59.3%) evolved into other syndromes or into atypical forms.
At the onset an initial diagnosis is possible in the majority of cases; epilepsy syndromes can be identified at the time of the initial diagnosis and at follow up this diagnosis has not to be revised in 90% of the cases.
评估儿童首次发作时特发性部分性癫痫早期综合征分类的可能性。
在这项观察性研究中,我们前瞻性地评估了298例年龄在1个月至17岁之间、因首次无诱因局灶性发作而连续转诊的患者。整个队列包括133例患者;最终分析是对107例(59例男性)个体进行的。首次发作时的年龄在2.3岁至13.0岁之间。所有患者的临床和脑电图数据由两名医生独立审查。对患者进行了至少5年的随访,平均随访期为6.9年。
首次发作后,80例(74.7%)儿童可诊断出特定综合征。具体而言,伴有中央颞区棘波的儿童癫痫(CECTS)占42.9%的病例,帕纳约托普洛斯综合征(PS)占28.9%,加斯东特发性儿童枕叶癫痫(ICOE-G)占2.8%。未分类病例占25.4%。随访结束时,80例儿童中有72例(90%)的诊断得到确认:BCECTS患者为89%,PS为90%,ICOE-G为100%;在未分类病例中,11例(40.7%)的诊断未改变,而16例(59.3%)发展为其他综合征或非典型形式。
在发病时,大多数病例可以做出初步诊断;癫痫综合征可以在初次诊断时确定,并且在随访中90%的病例无需修订该诊断。