Chiari I malformation: a rare cause of noncommunicating hydrocephalus treated by third ventriculostomy
- 1 November 2001
- journal article
- Published by Journal of Neurosurgery Publishing Group (JNSPG) in Journal of Neurosurgery
- Vol. 95 (5) , 783-790
- https://doi.org/10.3171/jns.2001.95.5.0783
Abstract
Hydrocephalus associated with Chiari I malformation is a rare entity related to an obstruction in the flow of cerebrospinal fluid (CSF) in the foramen of Magendie. Like all forms of noncommunicating hydrocephalus. it can be treated by endoscopic third ventriculostomy (ETV). The object of this study is to report a series of five cases of hydrocephalus associated with Chiari I malformation and to evaluate the use of ETV in the treatment of this anomaly. Five patients (four women and one man with a mean age of 29.6 years) underwent ETV for hydrocephalus associated with Chiari I malformation between April 1991 and February 1997. All patients had presented with paroxysmal headaches, which in two cases were associated with visual disorders. All patients had also presented with hydrocephalus (mean transverse diameter of the third ventricle 12.79 mm; mean sagittal diameter of the fourth ventricle 18.27 mm) with a mean herniation of the cerebellar tonsils at 13.75 mm below the basion-opisthion line. Surgery was performed in all patients by using a rigid endoscope. No complications occurred either during or after the procedure, except in one patient who experienced a wound infection that was treated by antibiotic medications. The mean duration of follow up in this study was 50.39 months. Four patients became completely asymptomatic and remained stable throughout the follow-up period. One patient required an additional third ventriculostomy after I year, due to secondary closure, and has remained stable since that time. Postoperative magnetic resonance images demonstrated a significant reduction in the extent of hydrocephalus in all patients (mean transverse diameter of the third ventricle 6.9 mm [p = 0.0035]; mean sagittal diameter of the fourth ventricle 10.32 mm [p = 0.007]), with a mean ascent of the cerebellar tonsils from 13.75 mm below the basion-opisthion line to 7.76 mm below it (p = 0.01). In addition, CSF flow was identified on either side of the orifice of the third ventriculostomy in all patients postoperatively. Results in this series confirm the efficacy of ETV in the treatment of hydrocephalus associated with Chiari I malformation. It is a reliable, minimally invasive technique that also provides a better understanding of the pathophysiology of this malformation.Keywords
This publication has 48 references indexed in Scilit:
- Arnold-Chiari malformation associated with sleep apnea and central dysregulation of arterial pressureActa Neurologica Scandinavica, 2009
- A new device for endoscopic third ventriculostomyJournal of Neurosurgery, 2000
- Audio-vestibular manifestations of Chiari malformation and outcome of surgical decompression: A case reportThe Journal of Laryngology & Otology, 1996
- Oscillopsia and horizontal nystagmus with accelerating slow phases following lumbar puncture in the Arnold‐chiari malformationAnnals of Neurology, 1993
- Endoscopic Third VentriculostomyNeurosurgery, 1990
- Documentation of fourth ventricle entrapment by metrizamide ventriculography with CT scanningJournal of Neurosurgery, 1981
- Percutaneous Third Ventriculostomy in the Management of Noncommunicating HydrocephalusNeurosurgery, 1980
- Size of posterior fossa in Chiari type 1 malformation in adultsActa Neurochirurgica, 1978
- Hydrocephalus due to membranous obstruction of the fourth ventricleJournal of Neurosurgery, 1971
- OBSERVATIONS ON THE FORAMEN OF MAGENDIE IN A SERIES OF HUMAN BRAINSBrain, 1948