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Thick Corpus Callosum in Children
Aviv Schupper1,2, Osnat Konen2,3, Ayelet Halevy1,2
1Department of Pediatric Neurology and Epilepsy Center, Schneider Children's Medical Center of Israel, Petach Tikva, Israel.
Insights
A thick corpus callosum (TCC) is rare in children and often not linked to severe outcomes, unlike in fetuses. This study found TCC in 1.3% of pediatric MRIs, associated with conditions like NF-1 and epilepsy.
Area of Science:
- Neuroimaging
- Pediatric Neurology
- Radiology
Background:
- A thick corpus callosum (TCC) is a fetal brain malformation often linked to severe outcomes.
- However, the clinical presentation and prognosis of TCC in older children appear significantly different.
Purpose of the Study:
- To investigate the clinical presentation and associated conditions of TCC in children.
- To determine if TCC in children carries the same grave prognosis as observed in fetuses.
Main Methods:
- Retrospective review of pediatric brain MRI studies.
- Inclusion criteria: diagnosis of TCC based on imaging.
- Clinical data collection and corpus callosum measurement.
Main Results:
- 34 children (1.3% of 2,552 MRIs) diagnosed with TCC.
- Associated conditions included neurofibromatosis-1 (NF-1), epilepsy, macrocephaly capillary malformation (MCM) syndrome, and autistic spectrum disorder.
- Measured CC thickness was comparable to adult norms; findings were not necessarily indicative of life-threatening conditions.
Conclusions:
- TCC is a rare finding in children, associated with diverse neuropathologies.
- Unlike fetal TCC, pediatric TCC is often a relatively benign finding.
- The clinical significance of TCC differs markedly between fetal and pediatric populations.
Background And Purpose:
A thick corpus callosum (TCC) can be associated with a very grave outcome in fetuses, but its clinical presentation in older children seems to be markedly different.
Methods:
The corpus callosum (CC) was defined as thick based on observations and impressions. We reviewed cases of children who were diagnosed as TCC based on brain magnetic resonance imaging (MRI) studies. The pertinent clinical data of these children were collected, and their CCs were measured.
Results:
Out of 2,552 brain MRI images, those of 37 children were initially considered as showing a TCC. Those initial imaging were reviewed by an experienced neuroradiologist, who confirmed the diagnosis in 34 children (1.3%): 13 had neurofibromatosis-1 (NF-1), 9 had epilepsy, 3 had macrocephaly capillary malformation (MCM) syndrome, 3 had autistic spectrum disorder, 1 had a Chiari-1 malformation, and 1 had increased head circumference. No specific neurologic disorder could be defined in seven children. The measured thickness of the CC in these children was comparable to those published in the literature for adults.
Conclusions:
A TCC is a rare brain malformation that can be found in neuropathologies with apparently diverse pathognomonic mechanisms, such as NF-1 and MCM. It is not necessarily associated with life-threatening conditions, instead being a relatively benign finding, different in nature from that reported in fetuses.
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