Description

Syringomyelia (sear-IN-go-my-EEL-ya) is a disorder in which a fluid-filled cyst forms within the spinal cord. Over time, this cyst, called a syrinx, expands and elongates, which can damage nerve and the spinal cord. Since the spinal cord connects the brain to nerves in the extremities, this damage may cause pain, weakness, and stiffness in the back, shoulders, arms, or legs.

Some people with a syrinx have no symptoms.  Symptoms vary among individuals but may include:

  • pain
  • progressive weakness in the arms and legs
  • headache
  • numbness or tingling
  • loss of sensitivity to pain or to hot and cold, especially in the hands
  • stiffness in the back, shoulders, neck, arms, or legs
  • problems with balance, as well as with bladder and bowel control.

Signs of the disorder tend to develop slowly. In most cases, the disorder is related to a congenital abnormality of the brain called a Chiari malformation, which causes brain tissue to protrude from its normal location in the back of the head and into the cervical or neck portion of the spinal canal. Syringomyelia may also occur as a complication of trauma, inflammation, spinal cord injury, hemorrhage, spinal cord tumors, or other conditions. Symptoms may appear months or even years after the initial injury, starting with pain, weakness, and sensory impairment originating at the site of trauma. Some cases of syringomyelia are seen in families, although this is rare.

Treatment

If there are no symptoms, syringomyelia is usually not treated and the person is monitored by a neurologist or neurosurgeon. Monitoring is also done in individuals of advanced age or in cases where there is no progression of symptoms. Surgery is usually recommended for individuals with symptomatic or progressive syringomyelia, with the type of surgery and its location dependent on the type of syrinx. Surgery is done to: provide more space at the bse of the skull and upper neck if there is a Chiari malformation prevent a syrinx from forming or expanding after an injury remove any obstruction that is blocking the flow of the crebrospinal fluid that bathes and protects the brain drain the syrinx, which can be accomplished using a catheter, drainage tubes, and valves. Syringomyelia can recur after surgery, making additional operations necessary.  Whether treated or not, many individuals with syringomyelia are told to avoid activities that involve straining.

Prognosis

Symptoms usually begin in young adulthood, with symptoms of one form usually beginning between the ages of 25 and 40 years. If not treated surgically (when needed), syringomyelia often leads to progressive weakness in the arms and legs, loss of hand sensation, and chronic, severe pain. Symptoms may worsen with straining or any activity that causes cerebrospinal fluid pressure to fluctuate. Some individuals may have long periods of stability. Surgery results in stabilization or modest improvement in symptoms for most individuals. Delay in treatment may result in irreversible spinal cord injury.

Research

Investigators at the National Institute of Neurological Disorders and Stroke (NINDS) are studying how syrinxes first form, as well as the mechanisms of the disorders. NINDS investigators have found that the normal flow of cerebrospinal fluid that occurs with each heartbeat is obstructed in people with syringomyelia. Surgical procedures that relieve this obstruction usually result in the syrinx becoming much smaller in size. Studies are also underway to better understand genetic factors that influence the development of Chiari I malformations and syringomyelia, as well as to identify the location of the gene(s) responsible for the malformation. Researchers hope to better understand the role of birth defects of the skull and brain malformations in the development of syringomyelia. Diagnostic technology is another area for continued research.   NINDS scientists are examining individuals who either have syringomyelia or are at risk of developing the disorder.  They are investigating the factors that influence its development, progression, and treatment by recording more than 5 years of symptoms, muscle strength, overall function, and magnetic resonance imaging (MRI) scan findings from individuals who receive standard treatment for syringomyelia.  Study results may allow scientists to provide more accurate recommendations to future individuals with syringomyelia regarding optimal surgical or non-surgical treatments. Information from the National Library of Medicine’s MedlinePlus Syringomyelia