Cranial Migration of a VP Shunt—A Routine Procedure with a Rare Complication!

Author:

Singh Aman1,Yadav Awadhesh1,Yadav Pritesh1,Ojha Bal Krishna1ORCID

Affiliation:

1. Department of Neurosurgery, King George's Medical University, Lucknow, Uttar Pradesh, India

Abstract

AbstractVentriculoperitoneal shunt is one of the commonest neurosurgical procedures associated with a high-rate complication. Moreover, the variety of complications are nonetheless astonishing. Shunt malfunction is considered the most common complication of this procedure, but a cranial migration of shunt leading to malfunction is extremely rare. We present a case of a 6-month-old male child who was initially managed with a right-sided medium-pressure ventriculoperitoneal shunt for aqueductal stenosis with hydrocephalus at the age of 3 months and presented to us with features of shunt malfunction owing to a cranial migration of the shunt assembly. Cranial migration of a ventriculoperitoneal shunt is an extremely rare complication. Its possible mechanism includes a large subgaleal space for the chamber, larger size burr hole, inadequate anchorage of the shunt assembly, and excessive neck movements of the child in the postoperative procedure.

Publisher

Georg Thieme Verlag KG

Subject

Materials Chemistry

Reference4 articles.

1. Complete intracranial migration of ventriculoperitoneal shunt: a common procedure with a rare complication;H Mehtab;Egypt J Neurosurg,2021

2. Complete intracranial migration of a ventriculoperitoneal shunt: rare complication of a common procedure;R K Sharma;Neurol India,2015

3. Cranial migration of complete ventriculoperitoneal shunt assembly;R D Nadkarni;J Clin Neurosci,2007

4. “Missing tube” of peritoneal shunt: migration of the whole system into ventricle;K Mori;Surg Neurol,1975

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