Posterior cord syndrome is a rare type of incomplete spinal cord injury that affects the dorsal columns of the spinal cord (found in the posterior—or backside—region of the spinal cord), responsible for the perception of fine-touch, vibration, sense of self-movement, and body positioning (proprioception).
The spinal cord is an important part of the central nervous system that serves as a highway for information to travel between the brain and the rest of the body. This information is transmitted by highly specialized spinal tracts or columns that carry sensory and motor information up and down the spinal cord. Ascending tracts, such as the posterior or dorsal columns and spinothalamic tract, carry sensory information from different parts of the body to the brain. Specifically, the dorsal columns carry delicate sensations, such as vibration, fine-touch (also known as discriminative touch), and proprioception. The spinothalamic tract, on the other hand, carries sensory information about pain, temperature, and crude touch (also known as non-discriminative touch). Descending tracts, such as the corticospinal tract, carry motor information from the brain towards the muscles of the trunk (torso) and limbs.Individuals with posterior cord syndrome typically present with sensory ataxia, or impaired voluntary movement coordination caused by a lack of proprioception. Sensory ataxia can result in decreased balance, poor coordination, unsteady walking, and frequent falls. These symptoms typically worsen in dark environments or when a person closes their eyes, as the body can no longer rely on sight to maintain balance. In addition, some individuals may experience sensory losses including impaired sensation of vibration and fine-touch, while their sensation of pain and temperature is preserved.
In some cases, large spinal cord lesions can also affect surrounding spinal tracts, such as those responsible for motor function and involuntary body functions (e.g. blood pressure, digestion, breathing). Involvement of these tracts can subsequently lead to various clinical manifestations, including muscle weakness and spasticity, decreased tendon reflexes, urinary or bowel incontinence, or low blood pressure, depending on the severity of the lesion.Posterior cord syndrome can be diagnosed with clinical tests to assess neurological function. Sensory problems can be assessed by asking an individual to identify different sensations (e.g. temperature, pain, vibration) while touching the skin with specific tools (e.g. dull needle, tuning fork, cotton swabs, etc.).
Additionally, Romberg’s test can be used to demonstrate sensory ataxia. This test is performed by asking an individual to close their eyes and stand straight with their feet together while the examiner looks for signs of loss of balance. If the individual is not able to stand straight without opening their eyes or swaying to either side, the result is considered to be positive for sensory ataxia.
Once posterior cord syndrome has been diagnosed, further tests are often required to identify the cause of spinal injury. This may include performing blood tests to check for vitamin deficiencies or markers of syphilis infection, as well as performing imaging tests to look for signs of demyelination, external compression of the spinal cord, or degenerative disorders.Copyright © 2024 Elsevier, its licensors, and contributors. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
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