Early classification of childhood focal idiopathic epilepsies: Is it possible at the first seizure?

被引:3
|
作者
Gaggero, Roberto [1 ]
Pistorio, Angela [2 ]
Pignatelli, Sara [3 ]
Rossi, Alessandra [4 ]
Mancardi, Maria Margherita [5 ]
Baglietto, Maria Giuseppina [5 ]
Striano, Pasquale [6 ]
Verrotti, Alberto [7 ]
机构
[1] San Paolo Hosp, Pediat Unit, Savona, Italy
[2] Serv Epidemiol & Biostat, Genoa, Italy
[3] ASL 3 Genova, Genoa, Italy
[4] Univ G dAnnunzio, Dept Pediat, Chieti, Italy
[5] G Gaslini Inst Children, Dept Child Neuropsychiat, Genoa, Italy
[6] Univ Genoa, Dept Neurosci Rehabil Ophtalmol Genet Maternal &, Pediat Neurol & Muscolar Dis Unit, Genoa, Italy
[7] Univ Perugia, Dept Pediat, I-06100 Perugia, Italy
关键词
Partial epilepsy; First seizure; Idiopathic epilepsy; Childhood epilepsy; Classification; Unclassified cases; PANAYIOTOPOULOS-SYNDROME; MISDIAGNOSIS; TERMINOLOGY; UNCERTAINTY; AGREEMENT; DIAGNOSIS; CHILDREN; EVENTS; EEG;
D O I
10.1016/j.ejpn.2014.01.011
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purposes: To evaluate the possibility of early syndrome classification of idiopathic partial epilepsies in children at the first seizure. Patients and methods: 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. Results: 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. Conclusions: 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. (C) 2014 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:376 / 380
页数:5
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