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Published on: August 22, 2012
Clinical aspects of neurocysticercosis in children
N M Morales1, S Agapejev, R R Morales
1Department of Neurology and Psychiatry, University of the State of São Paulo School of Medicine, Brazil.
Insights
Neurocysticercosis in children often presents with seizures and headaches. Many cases in this Brazilian study showed spontaneous resolution, suggesting cysticidal treatment may not always be necessary.
Area of Science:
- Neurology
- Infectious Diseases
- Pediatrics
Background:
- Neurocysticercosis is a significant public health concern, particularly in endemic regions.
- Pediatric neurocysticercosis presents unique clinical challenges and diagnostic considerations.
Purpose of the Study:
- To evaluate the clinical manifestations and outcomes of neurocysticercosis in children from a specific Brazilian region.
- To assess the efficacy of symptomatic versus cysticidal treatments in pediatric neurocysticercosis.
Main Methods:
- Retrospective analysis of 25 pediatric cases diagnosed with neurocysticercosis.
- Diagnosis confirmed through clinical evaluation, cerebrospinal fluid analysis, and neuroimaging.
- Review of treatment strategies, including symptomatic management and cysticidal drugs (praziquantel, albendazole).
Main Results:
- Predominantly male patients (72%) aged 1-11 years, residing in urban areas (68%).
- Common symptoms included epileptic seizures (72%), headache (60%), learning disability (24%), and behavioral changes (12%).
- High rates of remission (43.4%) and improvement (47.8%) were observed, with many cases showing spontaneous resolution without cysticidal drugs.
Conclusions:
- Neurocysticercosis should be considered in the differential diagnosis for children with neurological and developmental issues in endemic areas.
- Clinical presentation and outcomes in this cohort suggest a tendency towards spontaneous resolution, potentially reducing the need for aggressive cysticidal treatment.
- Further research is warranted to elucidate the natural history and optimal management strategies for pediatric neurocysticercosis.
Abstract:
The purpose of this report was to evaluate the clinical aspects of neurocysticercosis in children from a Brazilian region. A retrospective study of 25 children with this neuroparasitosis was performed. The diagnosis was based on clinical, cerebrospinal fluid, and neuroimaging findings. The patients were predominantly male (72%), were 1 to 11 years of age (average = 8 years, 6 months), and most resided in urban areas (68%). The more frequent manifestations were epileptic seizures (72%), headache (60%), learning disability (24%), behavioral changes (12%), psychomotor involution (8%), and intracranial hypertension (4%). The neurologic examination was normal in 80% of the patients. Twenty-two children received only symptomatic drugs. Three patients underwent treatment with cysticidal drugs, one with praziquantel and two with albendazole, with complete remission of the signs in one patient (33%) and improvement in two others (67%). Of the 25 patients, 43.4% had remission and 47.8% had improvement. We emphasize the need to consider neurocysticercosis as a differential diagnosis in children coming from endemic areas and presenting with learning disabilities, behavioral changes, and psychomotor involution. The clinical aspects in most of the children from the Botucatu region suggest a spontaneous resolution of neurocysticercosis without the need for cysticidal treatment.
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