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Acquired Chiari type I malformation managed by supratentorial cranial enlargement
Concezio Di Rocco1, Francesco Velardi
1Institute of Neurosurgery, Section of Pediatric Neurosurgery, Catholic University Medical School, Policlinico "A. Gemelli", Largo Gemelli 8, 00168, Rome, Italy. cdirocco@rm.unicatt.it
Insights
Acquired Chiari type-I malformation in children with CSF shunts may stem from craniocephalic disproportion. Cranial expansion resolved symptoms, suggesting this disproportion is key.
Area of Science:
- Neurosurgery
- Pediatric Neurology
- Cerebrospinal Fluid Dynamics
Background:
- Acquired Chiari type-I malformation in hydrocephalic patients was linked to cerebrospinal fluid (CSF) shunts.
- Previous studies focused on lumbo-peritoneal shunts and cranio-spinal pressure differentials.
Observation:
- Two adolescents with symptomatic acquired Chiari type-I malformation were studied.
- One patient had a lumbo-peritoneal shunt for pseudotumor cerebri; the other had a cysto-ventriculo-peritoneal shunt for a suprasellar arachnoid cyst.
Findings:
- Both patients experienced regression of clinical manifestations and cerebellar tonsillar herniation after supratentorial cranial expansion.
- No shunt manipulation was required to achieve these positive outcomes.
Implications:
- Secondary craniocephalic disproportion is a significant factor in acquired Chiari type-I malformation in pediatric patients with extrathecal CSF shunts.
- Supratentorial cranial expansion may be an effective treatment modality for this condition.
Introduction:
Acquired Chiari type-I malformation in hydrocephalic patients who have undergone surgical treatment was initially thought to depend on a craniocephalic disproportion induced by the cerebrospinal (CSF) shunt. However, most of the reports in the literature deal with children with lumbo-peritoneal shunts and emphasize the pathogenic role of the cranio-spinal pressure differential across the foramen magnum brought about by this type of shunt.
Method:
In the present report, the authors describe two further cases of symptomatic acquired Chiari type-I malformation observed in two adolescents operated on for correction of pseudotumor cerebri in one (lumbo-peritoneal shunt) and of a suprasellar arachnoid cyst (cysto-ventriculo-peritoneal shunt) in the other.
Results:
In both subjects, both the clinical manifestations and the cerebellar tonsillar herniation regressed after supratentorial cranial expansion, without the need for any manipulation of the shunt devices implanted earlier.
Discussion:
These results, together with the observation of the concomitant upward and downward herniation of the cerebellum in both patients, indicate that secondary craniocephalic disproportion plays a relevant role in the genesis of acquired Chiari type-I malformation in children bearing extrathecal CSF shunts.
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