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1.
Clin Infect Dis ; 43(12): 1565-77, 2006 Dec 15.
Artículo en Inglés | MEDLINE | ID: mdl-17109290

RESUMEN

BACKGROUND: Encephalitis is a complex syndrome, and its etiology is often not identified. The California Encephalitis Project was initiated in 1998 to identify the causes and further describe the clinical and epidemiologic characteristics of encephalitis. METHODS: A standardized report form was used to collect demographic and clinical data. Serum, cerebrospinal fluid, and respiratory specimens were obtained prospectively and were tested for the presence of herpesviruses, arboviruses, enteroviruses, measles, respiratory viruses, Chlamydia species, and Mycoplasma pneumoniae. The association between an identified infection and encephalitis was defined using predetermined, organism-specific criteria for confirmed, probable, or possible causes. RESULTS: From 1998 through 2005, a total of 1570 patients were enrolled. Given the large number of patients, subgroups of patients with similar clinical characteristics and laboratory findings were identified. Ten clinical profiles were described. A confirmed or probable etiologic agent was identified for 16% of cases of encephalitis: 69% of these agents were viral; 20%, bacterial; 7%, prion; 3%, parasitic; and 1%, fungal. An additional 13% of cases had a possible etiology identified. Many of the agents classified as possible causes are suspected but have not yet been definitively demonstrated to cause encephalitis; these agents include M. pneumoniae (n=96), influenza virus (n=22), adenovirus (n=14), Chlamydia species (n=10), and human metapneumovirus (n=4). A noninfectious etiology was identified for 8% of cases, and no etiology was found for 63% of cases. CONCLUSIONS: Although the etiology of encephalitis remains unknown in most cases, the recognition of discrete clinical profiles among patients with encephalitis should help focus our efforts toward understanding the etiology, pathogenesis, course, and management of this complex syndrome.


Asunto(s)
Encefalitis/fisiopatología , Proyectos de Investigación/normas , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Niño , Preescolar , Encefalitis/microbiología , Encefalitis/virología , Femenino , Humanos , Lactante , Masculino , Persona de Mediana Edad , Síndrome , Virus/aislamiento & purificación
2.
Neurology ; 63(8): 1489-93, 2004 Oct 26.
Artículo en Inglés | MEDLINE | ID: mdl-15505172

RESUMEN

The authors describe five cases of subacute sclerosing panencephalitis (SSPE) identified through the California Encephalitis Project that emphasize the importance of considering SSPE in the differential diagnosis of encephalitis, particularly among pediatric patients. SSPE was not suspected in the differential diagnosis of three of the cases until results of measles testing were known. The diagnosis of SSPE is often not considered by clinicians because of its rarity in the United States and the nonspecific clinical manifestations at onset.


Asunto(s)
Encefalitis/diagnóstico , Virus del Sarampión/inmunología , Panencefalitis Esclerosante Subaguda/diagnóstico , Adolescente , Biomarcadores/sangre , Biomarcadores/líquido cefalorraquídeo , Encéfalo/patología , Encéfalo/fisiopatología , Encéfalo/virología , Daño Encefálico Crónico/patología , Daño Encefálico Crónico/fisiopatología , Daño Encefálico Crónico/virología , Niño , Diagnóstico Diferencial , Errores Diagnósticos/prevención & control , Progresión de la Enfermedad , Electroencefalografía , Resultado Fatal , Femenino , Humanos , Inmunoglobulina G/líquido cefalorraquídeo , Masculino , Sarampión/sangre , Sarampión/líquido cefalorraquídeo , Sarampión/diagnóstico , Panencefalitis Esclerosante Subaguda/sangre , Panencefalitis Esclerosante Subaguda/líquido cefalorraquídeo
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