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A Case of Cerebral Tuberculoma who has been Suffered from Recurrent Idiopathic Pleural Effusion / 대한소아신경학회지
Journal of the Korean Child Neurology Society ; (4): 172-176, 2002.
Artigo em Coreano | WPRIM | ID: wpr-196798
ABSTRACT
Central nervous system(CNS) involvement by tuberculosis is uncommon in comparison to the involvement of other systems. Untreated tuberculous meningitis is characterized by progressive stupor and a fatal outcome within 4 to 8 weeks of the onset of symptoms. So rapid detection of Mycobacterium tuberculosis is of vital importance for these patients. In almost all patients with tuberculous meningitis, acid-fast bacteria are undetectable in the CSF. Culture techniques that permit the identification of the isolated mycobacterial species require several weeks. We report a case of tuberculous meningitis with intracranial tuberculoma in 8-year old male who experienced pleural effusion, repeatedly. CSF findings did not reveal diagnosis tuberculous meningitis. In MRI study, multiple intracranial tuberculomas were located at the cerebellum. Prolonged treatment with anti- tuberculous chemotherapy and high-dose corticosteroids led to complete recovery.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Derrame Pleural / Bactérias / Tuberculoma / Tuberculose / Tuberculose Meníngea / Imageamento por Ressonância Magnética / Cerebelo / Tuberculoma Intracraniano / Corticosteroides / Evolução Fatal Tipo de estudo: Estudo diagnóstico Limite: Criança / Humanos / Masculino Idioma: Coreano Revista: Journal of the Korean Child Neurology Society Ano de publicação: 2002 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Derrame Pleural / Bactérias / Tuberculoma / Tuberculose / Tuberculose Meníngea / Imageamento por Ressonância Magnética / Cerebelo / Tuberculoma Intracraniano / Corticosteroides / Evolução Fatal Tipo de estudo: Estudo diagnóstico Limite: Criança / Humanos / Masculino Idioma: Coreano Revista: Journal of the Korean Child Neurology Society Ano de publicação: 2002 Tipo de documento: Artigo