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1.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;39(10): 1365-1372, Oct. 2006. tab
Artigo em Inglês | LILACS | ID: lil-437819

RESUMO

We describe the relative frequency, clinical features, neuroimaging and pathological results, and outcome after pharmacological or surgical intervention for a series of pediatric patients with temporal lobe epilepsy (TLE) from an epilepsy center in Brazil. The medical records of children younger than 12 years with features strongly suggestive of TLE were reviewed from January 1999 to June 1999. Selected children were evaluated regarding clinical, EEG, and magnetic resonance imaging (MRI) investigation and divided into three groups according to MRI: group 1 (G1, N = 9), patients with hippocampal atrophy; group 2 (G2, N = 10), patients with normal MRI, and group 3 (G3, N = 12), patients with other specific temporal lesions. A review of 1732 records of children with epilepsy revealed 31 cases with TLE (relative frequency of 1.79 percent). However, when the investigation was narrowed to cases with intractable seizures that needed video-EEG monitoring (N = 68) or epilepsy surgery (N = 32), the relative frequency of TLE increased to 19.11 (13/68) and 31.25 percent (10/32), respectively. At the beginning of the study, 25 of 31 patients had a high seizure frequency (80.6 percent), which declined to 11 of 31 (35.5 percent) at the conclusion of the study, as a consequence of pharmacological and/or surgical therapy. This improvement in seizure control was significant in G1 (P < 0.05) and G3 (P < 0.01) mainly due to good postsurgical outcome, and was not significant in G2 (P > 0.1, McNemar's test). These results indicate that the relative frequency of TLE in children was low, but increased considerably among cases with pharmacoresistant seizures. Patients with specific lesions were likely to undergo surgery, with good postoperative outcomes.


Assuntos
Humanos , Masculino , Feminino , Pré-Escolar , Criança , Epilepsia do Lobo Temporal/cirurgia , Hipocampo/patologia , Lobo Temporal/patologia , Atrofia , Eletroencefalografia/métodos , Imageamento por Ressonância Magnética , Período Pós-Operatório , Estudos Retrospectivos , Resultado do Tratamento , Gravação em Vídeo
2.
Braz J Med Biol Res ; 39(10): 1365-72, 2006 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-16906314

RESUMO

We describe the relative frequency, clinical features, neuroimaging and pathological results, and outcome after pharmacological or surgical intervention for a series of pediatric patients with temporal lobe epilepsy (TLE) from an epilepsy center in Brazil. The medical records of children younger than 12 years with features strongly suggestive of TLE were reviewed from January 1999 to June 1999. Selected children were evaluated regarding clinical, EEG, and magnetic resonance imaging (MRI) investigation and divided into three groups according to MRI: group 1 (G1, N = 9), patients with hippocampal atrophy; group 2 (G2, N = 10), patients with normal MRI, and group 3 (G3, N = 12), patients with other specific temporal lesions. A review of 1732 records of children with epilepsy revealed 31 cases with TLE (relative frequency of 1.79%). However, when the investigation was narrowed to cases with intractable seizures that needed video-EEG monitoring (N = 68) or epilepsy surgery (N = 32), the relative frequency of TLE increased to 19.11 (13/68) and 31.25% (10/32), respectively. At the beginning of the study, 25 of 31 patients had a high seizure frequency (80.6%), which declined to 11 of 31 (35.5%) at the conclusion of the study, as a consequence of pharmacological and/or surgical therapy. This improvement in seizure control was significant in G1 (P < 0.05) and G3 (P < 0.01) mainly due to good postsurgical outcome, and was not significant in G2 (P > 0.1, McNemar's test). These results indicate that the relative frequency of TLE in children was low, but increased considerably among cases with pharmacoresistant seizures. Patients with specific lesions were likely to undergo surgery, with good postoperative outcomes.


Assuntos
Epilepsia do Lobo Temporal/patologia , Hipocampo/patologia , Lobo Temporal/patologia , Atrofia , Criança , Pré-Escolar , Eletroencefalografia/métodos , Epilepsia do Lobo Temporal/cirurgia , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino , Período Pós-Operatório , Estudos Retrospectivos , Resultado do Tratamento , Gravação em Vídeo
3.
Neuroradiology ; 46(10): 830-3, 2004 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-15300344

RESUMO

Castleman's disease is an atypical lymphoproliferative disorder that may present as a localized or multicentric form. The involvement of the central nervous system is rare. We describe here a case of Castleman's disease with involvement of the hypothalamus and meninges, presenting as hypopituitarism. Radiological and clinical pathological features are emphasized and a review of the literature is presented.


Assuntos
Encéfalo/diagnóstico por imagem , Encéfalo/patologia , Hiperplasia do Linfonodo Gigante/complicações , Hipopituitarismo/etiologia , Adulto , Hiperplasia do Linfonodo Gigante/diagnóstico por imagem , Hiperplasia do Linfonodo Gigante/patologia , Feminino , Humanos , Hipopituitarismo/diagnóstico por imagem , Hipopituitarismo/patologia , Radiografia
4.
Hippocampus ; 10(2): 169-80, 2000.
Artigo em Inglês | MEDLINE | ID: mdl-10791839

RESUMO

Dentate granule cells are generally considered to be relatively resistant to excitotoxicity and have been associated with robust synaptogenesis after neuronal damage. Synaptic reorganization of dentate granule cell axons, the mossy fibers, has been suggested to be relevant for hyperexcitability in human temporal lobe epilepsy and animal models. A recent hypothesis suggested that mossy-fiber sprouting is dependent on newly formed dentate granule cells. However, we recently demonstrated that cycloheximide (CHX) can block the mossy-fiber sprouting that would otherwise be induced by different epileptogenic agents and does not interfere with epileptogenesis in those models. Here, we investigated cell damage and neurogenesis in the dentate gyrus of pilocarpine- or kainate-treated animals with or without coadministration of CHX. Dentate granule cells were highly vulnerable to pilocarpine induced-status epilepticus (SE), but were hardly damaged by kainate-induced SE. CHX pretreatment markedly reduced the number of injured neurons after pilocarpine-induced SE. Induction of SE dramatically increased the mitotic rate of KA- and KA + CHX-treated animals. Induction of SE in animals injected with pilocarpine alone led to 2-7-fold increases in the mitotic rate of dentate granule cells as compared to 5- and 30-fold increases for pilocarpine + CHX animals. We suggest that such increased mitotic rates might be associated with a protection of a vulnerable precursor cell population that would otherwise degenerate after pilocarpine-induced SE. We further suggest that mossy-fiber sprouting and neurogenesis of granule cells are not necessarily linked to one another.


Assuntos
Fibras Musgosas Hipocampais/patologia , Estado Epiléptico/patologia , Animais , Antimetabólitos/análise , Bromodesoxiuridina/análise , Cicloeximida/farmacologia , Agonistas de Aminoácidos Excitatórios , Ácido Caínico , Masculino , Mitose/efeitos dos fármacos , Fibras Musgosas Hipocampais/química , Agonistas Muscarínicos , Pilocarpina , Inibidores da Síntese de Proteínas/farmacologia , Ratos , Ratos Wistar , Coloração e Rotulagem , Estado Epiléptico/induzido quimicamente
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