Agenesis of the Corpus Callosum and Aicardi Syndrome: A Neuroimaging and Clinical Comparison

• Published in: Pediatric neurology Vol. 68; pp. 44 - 48.e2
• Main Authors: Govil-Dalela, T., MD, Kumar, A., MD, PhD, DNB, Agarwal, R., MD, Chugani, H.T., MD
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.03.2017
• Subjects: Age of Onset; agenesis of corpus callosum; Agenesis of Corpus Callosum - diagnostic imaging; Agenesis of Corpus Callosum - physiopathology; Agenesis of Corpus Callosum - surgery; Aicardi syndrome; Aicardi Syndrome - diagnostic imaging; Aicardi Syndrome - physiopathology; Aicardi Syndrome - surgery; Brain - diagnostic imaging; Brain - physiopathology; Brain - surgery; Child, Preschool; Electroencephalography; epilepsy; Epilepsy - diagnostic imaging; Epilepsy - physiopathology; Epilepsy - surgery; Female; Follow-Up Studies; Glucose - metabolism; Humans; Infant; Infant, Newborn; Magnetic Resonance Imaging; Male; Neuroimaging; Neurology; Pediatrics; Positron-Emission Tomography; Retrospective Studies; Seizures - diagnostic imaging; Seizures - physiopathology; Seizures - surgery; epilepsy; agenesis of corpus callosum; positron emission tomography; Aicardi syndrome
• ISSN: 0887-8994; 1873-5150
• DOI: 10.1016/j.pediatrneurol.2016.12.002

Abstract Background Agenesis of the corpus callosum can occur in individuals with epilepsy, either in isolation or as part of various neurological conditions, such as Aicardi syndrome. In this study, we evaluated the clinical and neuroradiological differences between children with nonsyndromic agenesis of the corpus callosum and those with Aicardi syndrome. Methods We evaluated 31 children with epilepsy and agenesis of the corpus callosum (11 males, 20 females), 14 of whom had Aicardi syndrome (all females). We compared their clinical evaluations, radiological and electrophysiological findings, treatments, and their outcome. Results Median age at seizure onset was lower in the Aicardi syndrome group compared with nonsyndromic agenesis of the corpus callosum (two versus five months, P  = 0.006). The developmental impairment in terms of verbalization and ambulation was significantly worse in patients with Aicardi syndrome. The severity of magnetic resonance imaging (MRI) and glucose metabolism positron emission tomography (PET) involvement was more extensive in children with Aicardi syndrome than in nonsyndromic agenesis of the corpus callosum. In both groups, the PET scan showed a much more extensive area of involvement than suggested by the MRI scan. Four children underwent epilepsy surgery with significant improvement, but were not seizure free. Outcome was worse in those with PET showing abnormalities in the nonsurgical hemisphere despite normal appearance on MRI. All children who did not undergo surgery also continued to have seizures at last follow-up. Conclusions Children with Aicardi syndrome have earlier seizure onset, worse developmental outcome, and larger areas of brain abnormalities on neuroimaging compared with nonsyndromic agenesis of the corpus callosum patients. PET reveals larger area of abnormalities, compared with MRI. Although epilepsy surgery in agenesis of the corpus callosum may offer some palliative benefit in seizure frequency, none of our patients became seizure free.