Evidence-based commentary on the diagnosis, management, and further research of degenerative cervical spinal cord compression in the absence of clinical symptoms of myelopathy

Tomas Horak, Magda Horakova, Milos Kerkovsky, Marek Dostal, Petr Hlustik, Jan Valosek, Alena Svatkova, Petr Bednařík, Eva Vlckova, Josef Bednarik

Abstract

Degenerative cervical myelopathy (DCM) represents the final consequence of a series of degenerative changes in the cervical spine, resulting in cervical spinal canal stenosis and mechanical stress on the cervical spinal cord. This process leads to subsequent pathophysiological processes in the spinal cord tissues. The primary mechanism of injury is degenerative compression of the cervical spinal cord, detectable by magnetic resonance imaging (MRI), serving as a hallmark for diagnosing DCM. However, the relative resilience of the cervical spinal cord to mechanical compression leads to clinical-radiological discordance, i.e., some individuals may exhibit MRI findings of DCC without the clinical signs and symptoms of myelopathy. This degenerative compression of the cervical spinal cord without clinical signs of myelopathy, potentially serving as a precursor to the development of DCM, remains a somewhat controversial topic. In this review article, we elaborate on and provide commentary on the terminology, epidemiology, natural course, diagnosis, predictive value, risks, and practical management of this condition-all of which are subjects of ongoing debate.

Original languageEnglish
Article number1341371
JournalFrontiers in Neurology
Volume15
Pages (from-to)1-9
Number of pages9
ISSN1664-2295
DOIs
Publication statusPublished - May 2024

Keywords

  • cervical spinal canal stenosis
  • degenerative cervical cord compression
  • degenerative cervical myelopathy
  • magnetic resonance imaging
  • subclinical myelopathy

Fingerprint

Dive into the research topics of 'Evidence-based commentary on the diagnosis, management, and further research of degenerative cervical spinal cord compression in the absence of clinical symptoms of myelopathy'. Together they form a unique fingerprint.

Cite this