An update on Neurocysticercosis-related epilepsy

被引:6
|
作者
Espino, P. H. [1 ]
Couper, R. G. [2 ]
Burneo, J. G. [1 ,2 ]
机构
[1] Western Univ, Dept Clin Neurol Sci, Epilepsy Program, 339 Windermere Rd, London, ON N6A 5A5, Canada
[2] Western Univ, Schulich Sch Med & Dent, Neuroepidemiol Unit, London, ON, Canada
关键词
Neurocysticercosis; Seizures; Epilepsy; Taenia solium; Epileptogenesis; TEMPORAL-LOBE EPILEPSY; SOLITARY CYSTICERCUS GRANULOMA; SEIZURE RECURRENCE; DOUBLE-BLIND; CALCIFIED NEUROCYSTICERCOSIS; HIPPOCAMPAL SCLEROSIS; PERILESIONAL GLIOSIS; ALBENDAZOLE THERAPY; ANTIPARASITIC THERAPY; TOMOGRAPHIC LESIONS;
D O I
10.1016/j.clineuro.2022.107139
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Neurocysticercosis (NCC) is considered a public health problem in various parts of the world and is one of the preventable causes of epilepsy in developing countries. Epileptic seizures are the most common manifestation of NCC and can occur in any stage of the disease. The development of neurocysticercosis-related epilepsy continues to be poorly understood. Some potential explanations include a direct causal relationship, a result of an initial precipitating injury or linked to an external factor, and the remote possibility of coincidence. Various factors contributing to epileptogenesis have been proposed, including calcified lesions, residual gliosis, inflammatory immune response (influenced by genetic factors) and a potential association with hippocampal sclerosis. Treating NCC with antihelminthics, corticosteroids or antiseizure medications have ensured a large percentage of patients can adequately control their epileptic seizures. Cases of refractory epilepsy are rare. Finally, more prospective studies are still needed to have a better understanding of this disease.
引用
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页数:7
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