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Cystic Dilatation of the Fourth Ventricle : Case Report Kazutoshi Hida 1 , Yoshinobu Iwasaki 1 , Hiroshi Abe 1 1Department of Neurosurgery, Hokkaido University Keyword: Arnold-Chiari malformation , MRI , IVth ventricle , ventricular diverticulum pp.1169-1173
Published Date 1991/12/1
DOI https://doi.org/10.11477/mf.1406900288
  • Abstract
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The patient, a 25-year-old male, was admitted with a 2-year history of double vision and recurrent suboccipital headache. Neurological findings on admission revealed nystagmus, double vision in the far field, bilateral abducense palsy, weakness in the bilateral legs, hypalgesia and hypesthesia under the L5 level, gait disturbance and hypotonia of the anal sphincter. Plain skull X-ray showed marked digitalimpression and disappearance of the posterior clinoid process and the dorsum sella. Myelography disclosed a filling defect dorsal to upper and midcer-vical cord. Intraventricular injection of metrizamide outlined cystic dilatation and caudal migration of the fourth ventricle. Occipital craniectomy and laminectomy from Cl to C6 was performed. Opera-tive findings showed thickened arachnoid mem-branes and cystic expansion of the fourth ventricle lying dorsal to the cervical cord. Caudal portion of the ventricle was removed, and V-P shunt was placed into the fourth ventricle to maintain decom-pression of the cystic part of the fourth ventricle. This patient is considered to represent a case of cystic dilatation (or ventricular diverticulum) of the fourth ventricle in Arnold-Chiari malformation. We stress that posterior decompression with V-P shunting procedure is recommended as the treat-ment of choice for such Arnold-Chiari type II malformation.


Copyright © 1991, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 2185-405X 印刷版ISSN 0006-8969 医学書院

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