Neuropediatrics 2019; 50(04): 264-265
DOI: 10.1055/s-0039-1683381
Images in Neuropediatrics
Georg Thieme Verlag KG Stuttgart · New York

Appearance of FCD Type II Changes with Brain Maturation in Early Childhood

Puneet Jain
1   Division of Neurology, Department of Pediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada
,
Robyn Whitney
1   Division of Neurology, Department of Pediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada
,
Elysa Widjaja
2   Department of Diagnostic Imaging, The Hospital for Sick Children, Toronto, Ontario, Canada
› Author Affiliations
Further Information

Publication History

01 November 2018

04 January 2019

Publication Date:
01 March 2019 (online)

Cases

Two infants with drug-refractory epilepsy ([Table 1]) underwent magnetic resonance imaging (MRI). Case 1 showed subtle lower T2 signal in the right parietal operculum focal cortical dysplasia (FCD) at 12 months which became more apparent at 19 months and 5 years of age ([Fig. 1A]–[C]). In case 2, the right frontal FCD showed pronounced lower T2 signal at 8 weeks, and became less apparent at 5 months of age ([Fig. 1], D-E). Both cases were seizure-free after surgical resection.

Zoom Image
Fig. 1 Serial MRI scans in the two reported cases. Case 1: axial T2 MRI at 12-months of age (A) (1.5-Tesla) showed accelerated myelination (T2 hypointensity of the subcortical white matter) adjacent to the right parietal operculum (white arrow), at 19 months of age (B) showed increased T2 signal in the subcortical white matter of the right parietal operculum (white arrow), in keeping with focal cortical dysplasia, and at 5 years of age (C) showed subtle increased T2 signal in subcortical white matter (3-Tesla). Case 2: axial T2 MRI at 8 weeks of age (D) showing low T2 signal in the subcortical white matter of the right frontal lobe (1.5-Tesla) (arrowhead), which partially normalized at 5 months of age (E) (3-Tesla).
Table 1

Clinical characteristics of the two cases

Case 1

Case 2

Age at seizure onset

4 mo

1 mo

Sex

Female

Male

Seizure types

Staring, bilateral eye flickering, left arm posturing

Behavioral arrest; left arm jerking

Seizure frequency

Multiple times per d

Daily to weekly

Antiepileptic drugs tried

Carbamazepine, lamotrigine, topiramate, clonazepam

Phenobarbital, levetiracetam, Topiramate

Neurodevelopment

Global developmental delay; mild left hand weakness

Mild global developmental delay

MRI brain

The FCD in the right parietal operculum showed subtle lower T2 signal at 12 mo, and became more obvious (high T2 signal) at 19 mo and 5 y of age ([Fig. 1A]–[C]).

The FCD in the right frontal lobe showed obvious lower T2 signal at 8 wk of life, and became less apparent on at 5 mo of age ([Fig. 1] day e).

Scalp EEG–ictal onset

Right hemisphere–parasagittal

Right central

MEG

Cluster of dipoles in the right inferior frontal, inferior rolandic and angular gyrus

Cluster of dipoles in the rolandic and parietal region around the lesion

Age at epilepsy surgery

5 y

5 mo

Form of Invasive EEG monitoring

Subdural grid electrodes and depth electrodes

Intraoperative electrocorticography

Nature of surgery performed

Tailored resection of the lesion

Lesionectomy

Pathology

FCD type IIB

FCD type IIA

Seizure outcome

Seizure free at 12 y of age

Seizure free at 4 y of age

Abbreviations: EEG, Electroencephalography; FCD, focal cortical dysplasia; MEG, magneto-encephalography; MRI, magnetic resonance imaging.


Ethics

Informed consent was obtained from the parents for publication of this report.


 
  • References

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