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1.
Eur J Neurol ; 17(4): 589-93, 2010 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-20039938

RESUMO

BACKGROUND: Non-ketotic hyperglycemic chorea-ballism (NKHCB) had special reversible hyperintense on T1-weighted imaging (T1WI) lesion in comparsion to gray matter. However, the mechanism accounts for these lesions is still unclear. METHODS: Patients diagnosed with NKHCB were recruited from 2002 to 2004. The demographic, clinical, magnetic resonance imaging (MRI), and spectroscopy (MRS) features were recorded at acute and remission phase. RESULTS: In 18 patients with NKHCB, the blood sugar level at onset was significantly higher than that after being free from chorea-ballism (419.50 +/- 257.33 vs. 198.22 +/- 53.97 mg/dl, P = 0.001). The serum osmolality dropped from 318.33 +/- 15.21 mOsm/kg at onset to 292.50 +/- 7.85 mOsm/kg after recovery (P < 0.001). All patients displayed T1 hyperintense lesions at contralateral basal ganglia at acute phase. Eight patients receiving follow-up MRI at remission phase, all T1 hyperintense lesions at the basal ganglia regressed. The ratios between choline-containing compounds and creatine at acute and remission phases were significant higher in lesion than in normal side, respectively (acute phase: 1.12 +/- 0.23 vs. 0.72 +/- 0.28, P = 0.038; remission phase: 1.23 +/- 0.47 vs. 0.68 +/- 0.15, P = 0.013). The lactate peaks present at 1.3 ppm on the lesion side either in acute or in remission phase of most case. CONCLUSIONS: The clinical, MRI, and MRS findings suggest that the mechanisms responsible for NKHCB may be a reversible ischaemia insult potentiated by hyperglycemia.


Assuntos
Gânglios da Base/patologia , Coreia/metabolismo , Coreia/patologia , Hiperglicemia/metabolismo , Hiperglicemia/patologia , Doença Aguda , Idoso , Gânglios da Base/metabolismo , Colina/metabolismo , Coreia/sangue , Creatina/metabolismo , Feminino , Seguimentos , Lateralidade Funcional , Humanos , Hiperglicemia/sangue , Ácido Láctico/metabolismo , Imageamento por Ressonância Magnética , Espectroscopia de Ressonância Magnética , Masculino , Concentração Osmolar , Fatores de Tempo
2.
AJNR Am J Neuroradiol ; 31(8): 1506-7, 2010 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-20019108

RESUMO

MBD is a rare disorder strongly associated with alcoholism. It is characterized pathologically by demyelination and necrosis of the corpus callosum. MBD presents with severe neurologic deficits and significant sequelae developing in most survivors. We report a patient with total clinical recovery. Serial MR imaging demonstrated typical lesions with restricted diffusion in the acute stage and total resolution without atrophy or cystic change.


Assuntos
Alcoolismo/patologia , Imageamento por Ressonância Magnética , Doença de Marchiafava-Bignami/patologia , Recuperação de Função Fisiológica , Cerebelo/patologia , Corpo Caloso/patologia , Humanos , Cápsula Interna/patologia , Masculino , Pessoa de Meia-Idade , Remissão Espontânea
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