All issues > Volume 51(11); 2008

Original Article

Korean J Pediatr. 2008;51(11):1205-1210. Published online November 15, 2008.

The significance of corpus callosal size in the estimation of neurologically abnormal infants

Seung Taek ST Yu¹, Chang Woo CW Lee¹

¹Department of Pediatrics, Wonkwang University College of Medicine, Iksan, Korea

Correspondence Chang Woo CW Lee ,Email: chan33@wonkwang.ac.kr

Abstract

Purpose
: The development of the corpus callosum occupies the entire period of cerebral formation. The myelination pattern on magnetic resonance imaging (MRI) is very useful to evaluate neurologic development and to predict neurologic outcome in high risk infants. The thickness of the corpus callosum is believed to depend on the myelination process. It is possible to calculate the length and thickness of the corpus callosum on MRI. Thus, we can quantitatively evaluate the development of the corpus callosum. We investigated the clinical significance of measuring various portions of the corpus callosum in neonate with neurologic disorders such as hypoxic brain damage and seizure disorder.
Methods
: Forty-two neonates were evaluated by brain MRI. We measured the size of the genu, body, transitional zone, splenium, and length of the corpus callosum. Each measurement was divided by the total length of the corpus callosum to obtain its corrected size. The ratio of corpus callosal length and the anteroposterior diameter of the brain was also measured.
Results
: There was no statistical significance in the sample size of each part of the corpus callosum. However, the corrected size or the ratio of body of the corpus callosum correlated with periventricular leukomalacia and hypoxic ischemic encephalopathy.
Conclusion
: The abnormal size of the corpus callosum showed a good correlation with periventricular leukomalacia and hypoxic ischemic encephalopathy in neonates. We can predict clinical neurological problems by estimation of the corpus callosum in the neonatal period.

Keywords :Corpus callosum, Hypoxia-ischemia, Brain, Leukomalacia, Periventricular