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dc.contributor.authorSecchi, Thaís Leitept_BR
dc.contributor.authorBrondani, Rosanept_BR
dc.contributor.authorBragatti, José Augustopt_BR
dc.contributor.authorBizzi, Jorge Wladimir Junqueirapt_BR
dc.contributor.authorBianchin, Marino Muxfeldtpt_BR
dc.date.accessioned2022-10-26T04:47:08Zpt_BR
dc.date.issued2022pt_BR
dc.identifier.issn1664-2295pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/250299pt_BR
dc.description.abstractBackground: Neurocysticercosis (NCC) is a parasitic infection of the central nervous system that has been associated with mesial temporal lobe epilepsy with hippocampal sclerosis (MTLE-HS). However, this association has not been completely established. Objective: To evaluate the prevalence of calcified NCC (cNCC), its characteristics and a possible association between cNCC and MTLE-HS in a cohort of 731 patients with epilepsy. Methods: We review clinical, EEG and neuroimaging findings of 731 patients with epilepsy. From these, 659 had CT-scans and 441 patients had complete neuroimaging with CT-scans and MRI. In these patients, we review the prevalence and characteristic of epilepsy in cNCC and in MTLE-HS patients. Results: Forty-two (6.4%) of the 659 patients studied with CT-scans had cNCC. cNCC lesions were more frequent in women than in men (n = 33–78.6% vs. n = 09–21.4%, respectively; OR = 3.64;(95%CI = 1.71–7.69); p < 0.001). cNCC was more often in patients who developed epilepsy later in life, in older patients, in patients who had a longer history of epilepsy, and in those with a lower educational level. MTLE–HS was observed in 93 (21.1%) of 441 patients that had complete neuroimaging, and 25 (26.9%) of these 93 patients also had cNCC. Calcified NCC was observed in only 17 (4.9%) of the remaining 348 patients that had other types of epilepsy rather than MTLE-HS. Thus, in our cohort, cNCC was more frequently associated with MTLE-HS than with other forms of epilepsy, O.R. = 11.90;(95%CI = 6.10–23.26); p < 0.0001). Conclusions: As expected, in some patients the epilepsy was directly related to cNCC lesional zone, although this was observed in a surprisingly lower number of patients. Also, cNCC lesions were observed in other forms of epilepsy, a finding that could occur only by chance, with epilepsy probably being not related to cNCC at all. In this cohort, cNCC was very commonly associated with MTLE-HS, an observation in agreement with the hypothesis that NCC can contribute to or directly cause MTLE-HS in many patients. Given the broad world prevalence of NCC and the relatively few studies in this field, our findings add more data suggesting a possible and intriguing frequent interplay between NCC and MTLE-HS, two of the most common causes of focal epilepsy worldwide.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofFrontiers in neurology. [Lausanne]. Vol. 12 (Jan. 2022), 769356, 12 p.pt_BR
dc.rightsOpen Accessen
dc.subjectFatores desencadeantespt_BR
dc.subjectEpileptogenesisen
dc.subjectinitial precipitating injury (IPI)en
dc.subjectEsclerosept_BR
dc.subjectHippocampal sclerosisen
dc.subjectHipocampopt_BR
dc.subjectInflammation in epilepsyen
dc.subjectEpilepsiapt_BR
dc.subjectGender differences in epilepsyen
dc.subjectInflamaçãopt_BR
dc.subjectNeurocysticercosisen
dc.subjectDistribuição por sexopt_BR
dc.subjectNeurocisticercosept_BR
dc.titleEvaluating the association of calcified neurocysticercosis and mesial temporal lobe epilepsy with hippocampal sclerosis in a large cohort of patients with epilepsypt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001149836pt_BR
dc.type.originEstrangeiropt_BR


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