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1.
Neuropediatrics ; 35(6): 360-3, 2004 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-15627944

RESUMEN

OBJECTIVE: Reports on bilateral epilepsy surgical interventions are anecdotal because of the possible neurological deficits caused by them. METHODS: We report on a four-year-old amaurotic child with catastrophic epilepsy due to bilateral occipital cortical dysplasia. After video-EEG monitoring and intraoperative electrocorticography he underwent a two-step bilateral occipital lobectomy. RESULTS: The first resection resulted in only temporary seizure cessation; however, he became seizure-free after the second operation (follow-up: 20 months). CONCLUSION: Patients with catastrophic epilepsy due to bilateral epileptogenic lesions but without a high risk of additional postsurgical deficit may be good candidates for epilepsy surgery.


Asunto(s)
Epilepsias Parciales/cirugía , Lóbulo Occipital/cirugía , Ceguera/complicaciones , Enfermedad Catastrófica/terapia , Preescolar , Epilepsias Parciales/complicaciones , Humanos , Masculino , Reoperación
2.
Neuroradiology ; 42(5): 339-45, 2000 May.
Artículo en Inglés | MEDLINE | ID: mdl-10872153

RESUMEN

Among 527 MRI examinations of patients with a suspicion of epilepsy in 5 years, we found 32 cases of hippocampal malrotation (HIMAL). The characteristic features are: incomplete inversion of the hippocampus with and abnormally round shape; unilateral involvement of the whole hippocampus; normal signal intensity and size; blurred internal structure; an abnormal angle of collateral sulcus; abnormal position and size of the fornix; normal size of the temporal lobe; enlargement and particular configuration of the temporal horn, typical of corpus callosum agenesis; and a normal corpus callosum. In 7 cases (22%) HIMAL occurred together with developmental disorders. It was predominantly seen in men. The clinical features were varied. Based on some MRI features, the presence of developmental disorders, the male predominance, the frequently positive family history, and a review of the literature, we think HIMAL may be the consequence of a mild hemisphere developmental disorder. It is probably not the basic cause of epilepsy in such varied clinical setting, but may be a sign of a developmental disorder and can help in selecting patients for more meticulous investigation. It also may give some new understanding of brain development.


Asunto(s)
Cuerpo Calloso/anatomía & histología , Epilepsia/etiología , Hipocampo/anomalías , Adulto , Femenino , Hipocampo/crecimiento & desarrollo , Hipocampo/patología , Humanos , Imagen por Resonancia Magnética , Masculino , Factores Sexuales
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