Abstract
We describe the re-siting of ventriculoperitoneal shunts to the gallbladder in two children. The first child had a rare case of hydrocephalus associated with plasminogen deficiency. She had had multiple VP shunt revisions due to non-absorption of CSF from the peritoneum. The second had craniopharyngioma-related hydrocephalus with once again a non-absorbing peritoneum. We report no surgical complications in the revisions for both the cases, and there has been a subsequent follow-up of 46 and 28 months, respectively, without incident. A review of the relevant literature describing the use and the performance of ventriculocholecystic shunts in comparison with other ventricular shunts is considered.
Original language | English |
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Pages (from-to) | 505-508 |
Number of pages | 4 |
Journal | British Journal of Neurosurgery |
Volume | 27 |
Issue number | 4 |
DOIs | |
Publication status | Published - Aug 2013 |
Keywords
- hydrocephalus
- plasminogen deficiency
- ventriculocholecystic shunt
- ventriculobiliary shunt
- ventriculogallbladder shunt
- ventriculoperitoneal shunt
- VENTRICULO-GALLBLADDER SHUNT
- CHOLECYSTIC SHUNT
- HYDROCEPHALUS
- CHILDREN
- PERITONEAL