%0 Journal Article
%T The Role of Epilepsy Surgery in the Treatment of Childhood Epileptic Encephalopathy
%A Husam R. Kayyali
%A Ahmed Abdelmoity
%A Saleh Baeesa
%J Epilepsy Research and Treatment
%D 2013
%I Hindawi Publishing Corporation
%R 10.1155/2013/983049
%X Children with epileptic encephalopathy often have global impairment of brain function and frequent intractable seizures, which contribute further to their developmental disability. Many of these children have identifiable brain lesion on neurological imaging. In such cases, epilepsy surgery may be considered as a treatment option despite the lack of localized epileptic pattern on electroencephalogram (EEG). In this paper, we summarize the clinical features of epileptic encephalopathy syndromes and review the reported literature on the surgical approach to some of these disorders. 1. Introduction Epileptic encephalopathy is defined as a condition in which the epileptiform abnormalities themselves are believed to contribute to the progressive disturbance in cerebral function [1]. The report of the International League Against Epilepsy (ILAE) Task Force on Classification and Terminology includes eight syndromes under epileptic encephalopathies. One common feature among these epilepsy syndromes is the suboptimal response to treatment with antiepileptic medications. This invited the utilization of epilepsy surgery in selected patients who have structural brain lesion believed to be the cause of epilepsy. In this paper, we briefly review the clinical features of different epileptic encephalopathy syndromes and summarize the reported literature on the surgical approach and management of some of these disorders. 2. Classification of Epileptic Encephalopathies According to the age of onset, epileptic encephalopathy syndromes may be divided into two main groups. 2.1. Infantile Epileptic Encephalopathies 2.1.1. Ohtahara Syndrome First described in 1976 by Ohtahara, Ohtahara Syndrome is characterized by tonic seizures and burst suppression pattern on EEG [2]. Symptoms develop earlier than other forms of epileptic encephalopathies within the first 3 months of life, usually in the first 10 days. Etiology is unclear but it generally accompanies structural brain anomalies. Seventy-five percent of cases turn into West syndrome within 3 to 6 months, and some of these turn into Lennox-Gastaut syndrome. Seizures are resistant to treatment and generally have a poor prognosis. 2.1.2. Early Myoclonic Encephalopathy Has an early onset within the first few months of life in the form of erratic, fragmentary, or massive myoclonic seizures. Frequency varies from occasional to almost continuous myoclonus. Infants have severe delay in development, hypotonia, and disturbed alertness, sometimes with vegetative state. EEG is characterized by a burst-suppression pattern. Erratic
%U http://www.hindawi.com/journals/ert/2013/983049/