Central cord syndrome

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Central cord syndrome is the most common type of incomplete spinal cord syndrome and a common form, usually the result of spinal cord injurytrauma, accounting for ~10% of all spinal cord injuries. As the name implies, this syndrome is the result of a damage to the central portion spinal cord and in the setting of trauma most commonly affects the cervical cord. 

Epidemiology

Most often central cord syndrome occurs in the setting of trauma, and most offed older individuals with underlying cervical spondylosis. However, it may also be seen in younger persons who sustain substantial trauma to the cervical spine, for example during forceful football tackling such as when a player "spears" another with their head. 

Central cord syndrome is also seen in spinal cord tumours and other non-traumatic conditions (see below), and the epidemiology will match that of the underlying condition. 

Clinical presentation

Patients presentThe pattern of neurological deficit in patients with upper limb weakness, urinary retention (due to bladder dysfunction)central cord syndrome depends on the size of the injury which in turn affects which parts of the spinal cord are involved.

In smaller central lesions the spinothalamic tract fibers that cross the anterior white mater commissure are interrupted resulting in bilateral pain and sensorytemperature loss at the affected levels 12. Below these levels, cord function is intact. As the cervical region is most commonly affected, the neurological defect described as affecting a "cape" distribution (both arms and shoulders and upper chest but sparing the rest of the body) 12

In larger lesions, other parts of the cord are involved, including the corticospinal tracts, spinothalamic tracts, dorsal columns and spinal grey matter. The result is upper motor neuron pattern of deficit below the level of injury (due to interruption of descending corticospinal tracts) - spastic paralysis and urinary retention - and lower motor neurone pattern of deficit at the levels of injury (due to damage to the anterior horn cells) 12. The The upper extremities are classically more affected than the lower extremities, (due to upper limb fibres being located more centrally) with motor function more severely impaired than sensory function12.

Pathology

Central cord syndrome by definition primarily affectsis most often the centreresult of thetrauma but can also be seen in a variety of non-traumatic cord pathologies including: 

These are discussed separately, in their respective articles. 

Mechanism

Trauma

A hyperextension cervical injury is in individuals with degenerative canal stenosis is the most common mechanism for central cord syndrome, howeverand in such cases, it can be seen with other mechanisms including flexion. Occasionally it may be associated more chronically with syrinx the cord is pinched between disc and/or intramedullary spinal cord tumoursosteophytes anteriorly and ligamentum flavum hypertrophy posteriorly 812.

Associations

.

Other mechanisms including flexion, fracture dislocation and acute disc herniation can also result in a central cord syndrome and these are seen more frequently in younger individuals 12

Radiographic features

Plain radiograph and CT

MayOsseous imaging may be normal, show spondylosis, acquired/congenital canal stenosis, or fracture. The

The presence of an extension teardrop fracture should be a warning sign.

MRI

Findings depend upon the severity of trauma and presence of pre-existing canal stenosis, following features can be seen 11:

SignalTypically the cord will demonstrate the following signal characteristics

  • T1:
    • the affected region is usually of isointense signal compared to rest of cord or slightly hypointense
    • haemorrhagic contusion may have areas of high T1 signal
  • T2
    • increased signal centrally within the cord at the affected level (oedema/contusion)
    • haemorrhagic contusions will have variable signal with areas of low T2 eventually becoming apparent
  • T2* - SWI/GE: will show low signal and blooming if blood product 

History and etymology

Central cord syndrome was first described by R C Schneider et al. in 1954 1.

  • -<p><strong>Central cord syndrome </strong>is the most common type of <a href="/articles/incomplete-cord-syndromes">incomplete spinal cord syndrome</a> and a common form of <a href="/articles/spinal-cord-injury">spinal cord injury</a>, accounting for ~10% of all spinal cord injuries. As the name implies, this syndrome is the result of a damage to the central portion <a href="/articles/spinal-cord">spinal cord</a> and in the setting of trauma most commonly affects the cervical cord. </p><p>Epidemiology</p><p>Most often central cord syndrome occurs in older individuals with underlying cervical spondylosis. However, it may also be seen in younger persons who sustain trauma to the cervical spine, for example during forceful football tackling such as when a player "spears" another with their head. </p><p>Clinical presentation</p><p>Patients present with upper limb weakness, urinary retention (due to bladder dysfunction) and sensory loss below the level of the injury. The upper extremities are classically more affected than the lower extremities, with motor function more severely impaired than sensory function.</p><p>Pathology</p><p>Central cord syndrome by definition primarily affects the centre of the spinal cord and is frequently haemorrhagic.</p><p>Mechanism</p><p>A <a href="/articles/hyperextension-cervical-injuries">hyperextension cervical injury</a> is the most common mechanism for central cord syndrome, however, it can be seen with other mechanisms including flexion. Occasionally it may be associated more chronically with <a href="/articles/syrinx-1">syrinx </a>and/or <a href="/articles/intreamedullary-spinal-cord-tumors">intramedullary spinal cord tumours</a> <sup>8</sup>.</p><p>Associations</p><ul><li>
  • -<a href="/articles/extension-teardrop-fracture-1">hyperextension teardrop fracture:</a> can have associated acute traumatic CCS (ATCCS) in ~80% of cases <sup>7</sup>
  • -</li></ul><p>Radiographic features</p><p>Plain radiograph and CT</p><p>May be normal, show spondylosis, acquired/congenital canal stenosis, or fracture. The presence of an <a href="/articles/extension-teardrop-fracture-1">extension teardrop fracture</a> should be a warning sign.</p><p>MRI</p><p>Findings depend upon the severity of trauma and presence of pre-existing canal stenosis, following features can be seen <sup>11</sup>:</p><ul>
  • +<p><strong>Central cord syndrome </strong>is the most common type of <a href="/articles/incomplete-cord-syndromes">incomplete spinal cord syndrome</a>, usually the result of trauma, accounting for ~10% of all <a href="/articles/spinal-cord-injuries">spinal cord injuries</a>. As the name implies, this syndrome is the result of a damage to the central portion <a href="/articles/spinal-cord">spinal cord</a> and in the setting of trauma most commonly affects the cervical cord. </p><h4>Epidemiology</h4><p>Most often central cord syndrome occurs in the setting of trauma, and most offed older individuals with underlying cervical spondylosis. However, it may also be seen in younger persons who sustain substantial trauma to the cervical spine, for example during forceful football tackling such as when a player "spears" another with their head. </p><p>Central cord syndrome is also seen in spinal cord tumours and other non-traumatic conditions (see below), and the epidemiology will match that of the underlying condition. </p><h4>Clinical presentation</h4><p>The pattern of neurological deficit in patients with central cord syndrome depends on the size of the injury which in turn affects which parts of the spinal cord are involved.</p><p>In smaller central lesions the <a href="/articles/spinothalamic-tracts">spinothalamic tract fibers</a> that cross the <a href="/articles/anterior-spinal-commissure">anterior white mater commissure</a> are interrupted resulting in bilateral pain and temperature loss at the affected levels <sup>12</sup>. Below these levels, cord function is intact. As the cervical region is most commonly affected, the neurological defect described as affecting a "cape" distribution (both arms and shoulders and upper chest but sparing the rest of the body) <sup>12</sup>. </p><p>In larger lesions, other parts of the cord are involved, including the <a href="/articles/corticospinal-tract">corticospinal tracts</a>, <a href="/articles/spinothalamic-tracts">spinothalamic tracts</a>, <a href="/articles/dorsal-columns">dorsal columns</a> and spinal grey matter. The result is upper motor neuron pattern of deficit below the level of injury (due to interruption of descending corticospinal tracts) - spastic paralysis and urinary retention - and lower motor neurone pattern of deficit at the levels of injury (due to damage to the anterior horn cells) <sup>12</sup>. The upper extremities are classically more affected than the lower extremities (due to upper limb fibres being located more centrally) with motor function more severely impaired than sensory function <sup>12</sup>.</p><h4>Pathology</h4><p>Central cord syndrome is most often the result of trauma but can also be seen in a variety of non-traumatic cord pathologies including: </p><ul>
  • +<li>
  • +<a title="Intramedullary spinal cord tumours" href="/articles/intramedullary-spinal-tumours">intramedullary spinal cord tumours</a> (e.g. <a title="Spinal ependymoma" href="/articles/spinal-ependymoma">spinal ependymoma</a>)</li>
  • +<li>
  • +<a title="Syringohydromyelia" href="/articles/syringomyelia">syringohydromyelia</a>  (e.g. <a title="Chiari I malformation" href="/articles/chiari-i-malformation">Chiari I malformation</a>)</li>
  • +</ul><p>These are discussed separately, in their respective articles. </p><h5>Trauma</h5><p>A <a href="/articles/hyperextension-cervical-injuries">hyperextension cervical injury</a> in individuals with degenerative canal stenosis is the most common mechanism for central cord syndrome, and in such cases, the cord is pinched between disc and/or osteophytes anteriorly and ligamentum flavum hypertrophy posteriorly <sup>12</sup>. <a href="/articles/extension-teardrop-fracture-1">Hyperextension teardrop fracture</a> have associated acute traumatic central cord syndrome in ~80% of cases <sup>7</sup>.</p><p>Other mechanisms including flexion, fracture dislocation and acute disc herniation can also result in a central cord syndrome and these are seen more frequently in younger individuals <sup>12</sup>. </p><h4>Radiographic features</h4><h5>Plain radiograph and CT</h5><p>Osseous imaging may be normal, show spondylosis, acquired/congenital canal stenosis, or fracture. </p><p>The presence of an <a href="/articles/extension-teardrop-fracture-1">extension teardrop fracture</a> should be a warning sign.</p><h5>MRI</h5><p>Findings depend upon the severity of trauma and presence of pre-existing canal stenosis, following features can be seen <sup>11</sup>:</p><ul>
  • -</ul><p>Signal characteristics</p><ul>
  • +</ul><p>Typically the cord will demonstrate the following signal characteristics: </p><ul>
  • +<li>
  • +<strong>T1</strong><ul>
  • +<li>the affected region is usually of isointense signal compared to rest of cord or slightly hypointense</li>
  • +<li>haemorrhagic contusion may have areas of high T1 signal</li>
  • +</ul>
  • +</li>
  • -<strong>T1:</strong>  the affected region is usually of isointense signal compared to rest of cord</li>
  • +<strong>T2 </strong><ul>
  • +<li>increased signal centrally within the cord at the affected level (oedema/contusion)</li>
  • +<li>haemorrhagic contusions will have variable signal with areas of low T2 eventually becoming apparent</li>
  • +</ul>
  • +</li>
  • -<strong>T2: </strong>increased signal centrally within the cord at the affected level (oedema/contusion)</li>
  • -</ul><p>History and etymology</p><p>Central cord syndrome was first described by <strong>R C </strong><strong>Schneider</strong> et al. in 1954 <sup>1</sup>.</p>
  • +<strong>T2* - SWI/GE:</strong> will show low signal and blooming if blood product </li>
  • +</ul><h4>History and etymology</h4><p>Central cord syndrome was first described by <strong>R C </strong><strong>Schneider</strong> et al. in 1954 <sup>1</sup>.</p>

References changed:

  • 12. Kunam VK, Velayudhan V, Chaudhry ZA, Bobinski M, Smoker WRK, Reede DL. Incomplete Cord Syndromes: Clinical and Imaging Review. (2018) Radiographics : a review publication of the Radiological Society of North America, Inc. 38 (4): 1201-1222. <a href="https://doi.org/10.1148/rg.2018170178">doi:10.1148/rg.2018170178</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/29995620">Pubmed</a> <span class="ref_v4"></span>
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