Perilesional brain oedema and seizure activity in patients with calcified neurocysticercosis: a prospective cohort and nested case-control study

Theodore E. Nash, E. Javier Pretell, Andres G. Lescano, Javier A. Bustos, Robert H. Gilman, Armando E. Gonzalez, Héctor H. Garcia

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

160 Citas (Scopus)

Resumen

Background: Cysticercosis due to Taenia solium is a cause of adult-acquired seizures and epilepsy even in patients with only calcified larval cysts. Transient perilesional brain oedema is seen around the calcified foci but its importance, association with seizures, incidence, and pathophysiology are unknown. Methods: 110 patients with only calcified lesions and a history of seizures or severe headaches were followed prospectively in a cohort design to assess the incidence of seizure relapse. In a nested case-control substudy, perilesional oedema was assessed by MRI at the time of seizure in symptomatic patients and in matched asymptomatic controls taken from the study population. Findings: Between November, 1999, and December, 2006, 29 patients had an incident seizure during a median follow up of 32·33 (SD 19·99) months, with an estimated 5-year seizure incidence of 36% (95% CI 25% to 49%). 24 of 29 (83%) patients with seizure relapse had an MRI evaluation within 5 days of the event; perilesional oedema was seen in 12 patients (50%) compared with two (9%) of 23 asymptomatic matched controls. Interpretation: Perilesional oedema is common and associated with episodic seizure activity in patients with calcified neurocysticercosis. Our findings are probably representative of symptomatic patients in regions where T solium neurocysticercosis is endemic and suggest a unique and possibly preventable cause of seizures in this population. Funding: US National Institute of Allergy and Infectious Diseases; US National Institutes of Health; Fogarty International Center.

Idioma originalInglés
Páginas (desde-hasta)1099-1105
Número de páginas7
PublicaciónThe Lancet Neurology
Volumen7
N.º12
DOI
EstadoPublicada - dic. 2008

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