Ak. Baranwal et al., Seizure recurrence in children with focal seizures and single small enhancing computed tomographic lesions: Prognostic factors on long-term follow-up, J CHILD NEU, 16(6), 2001, pp. 443-445
Single small enhancing computed tomographic (CT) lesions are common in chil
dren with focal seizures. There is a paucity of information regarding their
long-term outcome and prognostic factors for seizure recurrence. The objec
tive of this work was to study the frequency of seizure recurrence in child
ren with single small enhancing computed tomographic lesions and to identif
y prognostic factors, if any, for seizure recurrence. A prospective long-te
rm follow-up was conducted at the Advanced Pediatric Center, Postgraduate I
nstitute of Medical Education and Research, an urban tertiary care teaching
hospital. Sixty-three children between 2 and 12 years of age with focal se
izures for less than 3 months and single small enhancing computed tomograph
ic lesions were enrolled in a randomized, double-blind, placebo-controlled
trial of albendazole therapy and followed up for 4 years. On long-term foll
owup, the albendazole and placebo groups were left with 29 and 28 children,
respectively. After several months of seizure-free period, antiepileptic d
rug was tapered off. Children with relapse underwent magnetic resonance ima
ging examination. All children were followed up for at least 18 months afte
r stopping of the antiepileptic drug. Seizure recurrence was seen in three
children each in both groups, after a mean interval of 6.4 weeks after stop
ping the antiepileptic drug. Magnetic resonance imaging revealed persistent
chronic granuloma in 2 and calcified granuloma in 4 children. Residual les
ions were significantly correlated with seizure recurrence. In children who
se lesions completely disappeared, no seizure recurrence was seen even duri
ng shorter periods of antiepileptic drug treatment. Seizure recurrence was
seen in a small number of children with focal seizures and single small enh
ancing computed tomographic lesions. It appears to be related to either a p
ersistent or a calcified lesion.