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.
Abstract