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. 2016 Nov 9;10(11):e0005115. doi: 10.1371/journal.pntd.0005115

Table 1. –Clinical findings of the cohort of patients studied from 1995 to 2010.

Demographic data
    Age at diagnosis (mean, sd) 40 years, 9.8
    Sex 20 men (55.5%); 16 female (45.5%)
    Habitation 28 urban (78%); 8 rural (22%)
Initial clinical symptoms and signs
    Headache 28 (77.8%)
    Nausea/vomiting 21 (58.3%)
    Seizures 16 (44.4%)
    Fatigue 8 (22.2%)
    Papilledema 17 (47.2%)
    Motor deficits 8 (22.2%)
    Meningeal irritation 7 (19.4%)
    Cranial nerve deficits 5 (13.9%)
Cognitive impairment 4 (11.1%)
    Ataxia/dysmetria 2 (5.6%)
Initial clinical syndromes
    Raised intracranial pressures 21 (58.3%)
    Seizures 16 (44.4%)
    Headache (w/o raised intracranial pressure) 9 (25%)
Cysticercotic meningitis 7 (19.4%)
Clinical syndromes during all the follow-up period
    Raised intracranial pressure 27 (75%)
    Cysticercotic meningitis 26 (72.2%)
    Seizures 22 (61.1%)
    Headache (w/o raised intracranial pressure) 18 (50%)
Treatment modalities
    Anti-parasitic drugs 22 (61.1%)
    Corticosteroids 28 (77.8%)
    Ventriculoperitoneal shunt 23 (63.9%)
    Microsurgical removal of cysts 7 (19.4%)
    Endoscopic approaches 7 (19.4%)