Rapidly Deteriorating Degenerative Cervical Myelopathy Following Ventricular Shunt Revision for Hydrocephalus: Case Report.

case cervical cervical myelopathy disk disk herniation gait ligament myelopathy neck ossification of posterior longitudinal ligament spinal spine spondylosis stenosis woman women

Journal

Interactive journal of medical research
ISSN: 1929-073X
Titre abrégé: Interact J Med Res
Pays: Canada
ID NLM: 101598421

Informations de publication

Date de publication:
28 Aug 2023
Historique:
received: 16 04 2023
accepted: 24 07 2023
revised: 06 07 2023
medline: 28 8 2023
pubmed: 28 8 2023
entrez: 28 8 2023
Statut: epublish

Résumé

A female patient in her early 40s presented with a several-month history of gait unsteadiness and dragging her left leg. She had a background of congenital hydrocephalus, treated with a ventriculoatrial shunt. On examination, she had increased tone and brisk reflexes in the lower limbs and a positive Hoffmann sign. A computed tomography (CT) scan and shunt series x-rays identified hydrocephalus secondary to a disconnected shunt. Magnetic resonance imaging (MRI) of her cervical spine was also performed as part of the workup for her presenting symptoms and demonstrated features compatible with degenerative cervical myelopathy (DCM). The patient subsequently underwent a shunt revision. Following the operation, her walking and hand function deteriorated over a period of several weeks. She consequently underwent an anterior cervical decompression and fusion for DCM, which partially improved her symptoms. The sequence of events suggests that the shunt surgery may have precipitated a worsening of the DCM. Possible explanations include spinal cord injury related to neck extension or hypoperfusion during intubation and general anesthesia or the loss of cerebrospinal fluid cushioning following the reinstitution of effective cerebrospinal fluid shunting. Surgeons should be alert to this possibility and offer prompt surgical intervention for DCM if required.

Identifiants

pubmed: 37639306
pii: v12i1e48222
doi: 10.2196/48222
pmc: PMC10495845
doi:

Types de publication

Case Reports

Langues

eng

Pagination

e48222

Informations de copyright

©Tanzil Rujeedawa, Oliver Mowforth, Mark Kotter, Benjamin Davies. Originally published in the Interactive Journal of Medical Research (https://www.i-jmr.org/), 28.08.2023.

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Auteurs

Tanzil Rujeedawa (T)

Division of Neurosurgery, Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom.

Oliver Mowforth (O)

Division of Neurosurgery, Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom.

Mark Kotter (M)

Division of Neurosurgery, Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom.

Benjamin Davies (B)

Division of Neurosurgery, Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom.

Classifications MeSH