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Follow-up study of macrocephalic children with enlargement of the subarachnoid space
J L Gherpelli1, V Scaramuzzi, M L Manreza
1Department of Neurology, Clinics Hospital, University of Sao Paulo Medical School, Brasil.
Insights
Enlargement of the subarachnoid space (ESAS) in macrocephalic children is often benign. Most children with ESAS and macrocephaly show long-term persistence of these findings.
Area of Science:
- Pediatric Neurology
- Neuroimaging
- Developmental Pediatrics
Background:
- Macrocephaly in infants can be associated with various neurological conditions.
- Enlargement of the subarachnoid space (ESAS) is a finding observed in some macrocephalic infants.
- The long-term neurodevelopmental outcomes for infants with ESAS are not well-established.
Purpose of the Study:
- To prospectively evaluate the neurodevelopmental outcomes and neuroimaging findings in macrocephalic children with ESAS.
- To determine the natural history and potential resolution of ESAS in this cohort.
Main Methods:
- Prospective follow-up of 18 macrocephalic children diagnosed with ESAS.
- Neurological examinations and occipitofrontal circumference (OFC) measurements were performed.
- Serial CT-scans were utilized to assess changes in subarachnoid space and ventricular size.
Main Results:
- 11% of children exhibited neurological abnormalities at follow-up.
- 45% of children had their OFC normalize during the follow-up period.
- CT-scans showed resolution in 3/11, improvement in 2/11, and stability in 6/11 cases of ESAS.
Conclusions:
- ESAS in macrocephalic children is frequently a benign condition.
- While ESAS and macrocephaly may persist, significant adverse neurodevelopmental outcomes are uncommon.
- No cases of intracranial hypertension were observed in this cohort.
Abstract:
Eighteen macrocephalic children with enlargement of the subarachnoid space (ESAS), with or without mild ventricular dilatation, were followed prospectively to a mean age of 56 months. All were born at term, with uneventful neonatal period and negative tests for congenital infections. There were 17 boys and 1 girl and the mean follow-up period was 46 months (8-58 months). The initial neurologic evaluation, between ages of 2 to 33 months, disclosed abnormalities in 2 cases. At the follow-up one was still abnormal and the other had a normal neurological examination. Another child, who had a normal neurological examination at the age of 5 months, at the age of 7 years and 7 months had an IQ of 77. Thus the abnormality rate at follow-up was 11%. The OFC returned to the normal range in 45% of the children at the follow-up period. There were no cases of intracranial hypertension. One infant had subdural taps performed at the age of 13 months that disclosed a fluid with the same characteristics as the CSF. All the children had a CT-scan performed at the beginning of the study that revealed a large subarachnoid space; in 77% it was associated with mild ventricular dilatation. Eleven had CT-scans repeated, during the study period, which showed resolution of the process in 3 cases, improvement in 2, and unchanged in 6. We conclude that enlargement of the subarachnoid space in macrocephalic children is often a benign entity. ESAS and macrocephaly will still be present in the majority of children in the long-term follow-up.
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