Schizencephaly:Correlation of Clinical Outcome with Imaging Findings.
- Author:
Se Hyuck PARK
1
;
Yong Joon CHO
;
Kyu Ho LEE
;
Sae Moon OH
Author Information
1. Department of Neurosurgery, Hallym University College of Medicine, Seoul, Korea.
- Publication Type:Original Article
- Keywords:
Schizencephaly;
Neuronal migration;
Gray matter-lined cleft;
Polymicrogyria;
Gray matter heterotopia
- MeSH:
Brain;
Cerebrum;
Congenital, Hereditary, and Neonatal Diseases and Abnormalities;
Frontal Lobe;
Humans;
Lateral Ventricles;
Lip;
Malformations of Cortical Development;
Neurons;
Optic Nerve;
Paresis;
Retrospective Studies;
Seizures;
Septum Pellucidum;
Skull
- From:Journal of Korean Neurosurgical Society
1996;25(12):2465-2471
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Schizencephaly is an infrequent congenital disorder of neuronal migration characterized by gray matter-lined clefts that extent through the entire cerebral hemisphere, from the ependymal lining of the lateral ventricle to the pial covering of the cortex. We have studied seven patients with schizencephaly retrospectively to correlate clinical outcome with the type, Size, and location of the clefts and to find associated brain anomalies. Three patients had bilateral clefts(one with two open lip clefts and the other two with a left open lip cleft and a right closed lip cleft), another two patients had left unilateral open lip clefts, and the rest two patients had right closed lip clefts. Clinically, these patients presented motor dysfunction such as hemiparesis, seizures, and variable developmental delay. Patients with bilateral clefts, particularly open lip type, had worse motor and developmental impairment than those with unilateral clefts. Patient with unilateral medium open lip cleft had worse motor and inte llectual impairment than those with unilateral closed lip clefts or small open lip cleft. All patients with frontal lobe involvement had motor dysfunction. Absence of septum pellucidum, gray matter heterotopia, polymicrogyria, and hypoplasia of optic nerves were also frequently found to be associated with schizencephaly. Three patients with skull canges such as enlargement of the hemicranium or erosion of the inner table of the skull were shunted but only one patient improved in the imaging study. We conclude that the severity of patient's symptoms is related to the amount, type, and location of the involved brain.
