Rasmussen Encephalitis: longterm outcome after surgery

• Main Author: Terra, Vera Cristina
• Publication Date: 2010
• Other Authors: Machado, Helio Rubens, Oliveira, Ricardo dos Santos, Neder, Luciano, Souza-Oliveira, Cecília, Escorsi-Rosset, Sara, Yacubian, Elza Márcia Targas [UNIFESP], Naffah-Mazzacoratti, Maria da Graca [UNIFESP], Scorza, Carla Alessandra [UNIFESP], Cavalheiro, Esper Abrão [UNIFESP], Scorza, Fulvio Alexandre [UNIFESP], Sakamoto, Américo Ceiki [UNIFESP]
• Format: Article
• Language: eng
• Source: Repositório Institucional da UNIFESP
• Download full: http://dx.doi.org/10.1590/S1676-26492010000200004; http://repositorio.unifesp.br/handle/11600/5571
• topic: Rasmussen encephalitis; intractable epilepsy; pediatric population and epilepsy surgery; Encefalite de Rasmussen; epilepsia intratável; população pediátrica e cirurgia de epilepsia

BACKGROUND AND PURPOSE: Rasmussen Encephalitis (RE) is characterized by intractable epilepsy, progressive hemiparesis and unilateral hemispheric atrophy. The progression of the symptoms usually occurs within months to few years. Antiepileptic drugs are usually not effective to control disease progression and epilepsy surgery in the form of hemispheric disconnection has been considered the treatment of choice. This work describes the clinical and electrographic analyses, as well as the post-operative evolution of patients with RE. PATIENTS AND METHODS: This work includes all the patients with RE evaluated from January 1995 to January 2008 by the Ribeirão Preto Epilepsy Surgery Program (CIREP) considering demographic data, interictal and ictal electroencephalographic (EEG) findings; anatomo-pathological findings and clinical outcome. RESULTS: Twenty-five patients were evaluated, thirteen were female. Mean age of epilepsy onset was 4.4±2.0 years. There were no differences between patients with slow and fast evolution with respect to age of epilepsy onset (p=0.79), age at surgery (p=0.24), duration of epilepsy (0.06), and follow-up (p=0.40). There were no correlations between the presence of bilateral EEG abnormalities or the absence of spikes and post-operative seizure outcome (p=0.06). Twenty-three patients underwent surgery. The mean follow-up was 75.3 months. Eleven patients had total seizure control. Twelve individuals persisted with seizures consisting of mild facial jerks (6 patients), occasional hemigeneralized tonic-clonic seizures (3 patients), and frequent tonic-clonic seizures (3 patients). Mental and language impairment was observed in 15 and 12 patients, after surgery, respectively. CONCLUSIONS: This retrospective study reported the clinical and electrographic analysis, as well as the evolution of 23 patients with RE. Fourteen patients achieved satisfactory seizure control, three patients had partial response to surgery, and five patients had maintenance of the pre-operative condition. All patients with left side involvement presented with some language and cognitive disturbance.