All issues > Volume 53(1); 2010
- Case Report
- Korean J Pediatr. 2010;53(1):106-110. Published online January 15, 2010.
- A case of hippocampal sclerosis diagnosed as cortical dysplasia due to preoperative brain MRI finding
- Jun Seok JS Lee1, Kyo Ryung KR Kim1, Jeong Tae JT Kim1, Min Jung MJ Choi1, Young Mock YM Lee1, Heung Dong HD Kim1, Joon Soo JS Lee1, Dong Seok DS Kim2, Tae Seong TS Kim3
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1Department of Pediatrics, Severance Children`s Hospital, Yonsei University College of Medicine, Seoul, Korea
2Department of Neurosurgery, Yonsei University College of Medicine, Seoul, Korea
3Department of Pathology, Yonsei University College of Medicine, Seoul, Korea - Correspondence Joon Soo JS Lee ,Tel: +82.2-2228-2063, Fax: +82.2-393-9118, Email: joonsl96@yuhs.ac
- Abstract
- Hippocampal sclerosis (HS) is one of the most common features of intractable temporal lobe epilepsy. Generally it can be identified through brain magnetic resonance imaging (MRI) with high degree of sensitivity and specificity. Typical brain MRI findings of HS are hippocampal atrophy with hyperintense signal confined to the lesion. On the other hand cortical dysplasia exhibits blurring of the gray-white matter junction and abnormal white matter signal intensity. We present a case where preoperative brain MRI strongly suggested the presence of diffuse cortical dysplasia in the left temporal lobe but postoperative pathology revealed the temporal lesion to be unremarkable except for hippocampal sclerosis.
Keywords :Hippocampus, Cortical dysplasia, Epilepsy, Surgery, MRI