Neuroscience Clerkship

 

 

CENTRAL CORD SYNDROME

 

 

The initial signs and symptoms caused by central cord lesion are often related to dysfunction of the fibers that pass through the anterior white commissure (i.e., the crossing spinothalamic tracts at that level). This results in a cape-like distribution of decreased sensation to pin and temperature at the level of the lesion.  Motor function as well as vibration is preserved in small lesions.

Further symptoms are caused if the lesion expands into additional cord regions. Lesions that include the anterior gray matter of the spinal cord may destroy the anterior horn cells, causing weakness and wasting of muscles (lower motor neuron signs) at the involved levels. Further enlargement of the area of the lesion may result in involvement of the spinothalamic tracts. Because spinothalamic tract fibers serving the sacral areas travel most superficially in the spinal cord, an expanding central cord lesions will cause increasing areas of anesthesia, but with a tendency spare the sacral area, as these fibers are most distant from the center of the cord. Thus, an expanding cervical central cord lesion may begin by causing an area of cape-like anesthesia involving the arms but with progressively descending sensory involvement to the point that only the saddle area is spared ("sacral sparing").

The most common causes of such central lesions are syringomyelia, intrinsic cord tumors, trauma, and demyelination.

Above: Cape-like sensory loss to pain and temperature that occurs in a small central cord lesion in the cervical and upper thoracic cord.