A case of megalencephalic leukoencephalopathy with subcortical cysts.
10.3345/kjp.2008.51.12.1342
- Author:
Eun Young PARK
1
;
Young Ok KIM
;
Ji Youn KIM
;
Chae Young YEO
;
Hee Jo BAEK
;
Chan Jong KIM
;
Eun Young KIM
;
Young Jong WOO
Author Information
1. Department of Pediatrics, School of Medicine, Chonnam National University, Gwangju, Korea. ik052@unitel.co.kr
- Publication Type:Case Report
- Keywords:
Megalencephalic leukoencephalopathy with subcortical cysts;
Developmental disabilities
- MeSH:
Ataxia;
Basal Ganglia;
Brain;
Cerebellum;
Cysts;
Developmental Disabilities;
Follow-Up Studies;
Head;
Hereditary Central Nervous System Demyelinating Diseases;
Humans;
Leukoencephalopathies;
Macrocephaly;
Muscle Spasticity;
Parietal Lobe;
Seizures
- From:Korean Journal of Pediatrics
2008;51(12):1342-1345
- CountryRepublic of Korea
- Language:English
-
Abstract:
Megalencephalic leukoencephalopathy with subcortical cysts (MLC) is a rare white matter disorder, first described in the early 1990s. The brain in patients with MLC appears swollen on MRI, with diffuse white matter abnormalities; in addition, there is an invariable presence of subcortical cysts, primarily in the anterior temporal region sparing the deep white matter, basal ganglia, thalami, and cerebellum. Patients with MLC present with macrocephaly and neurological abnormalities such as motor deterioration, ataxia, spasticity, and cognitive deficits. We report a twenty-month-old boy who presented with seizures and macrocephaly, delay in development, and abnormal brain MRI findings compatible with the diagnosis of MLC. The brain MRI revealed bilateral hypersignal intense subcortical white matter regions in the frontal, temporal, and parietal lobes on T2-weighted images, which were not yet associated with cystic changes. During follow-up, the frequency of seizures decreased after anticonvulsant medication was started, but the head circumference remained above the 97th percentile, and the patient continued to have developmental delay.
