Syringomyelia is damage to the spinal cord due to a fluid-filled hole that forms in the cord.
Causes, incidence, and risk factors
The fluid buildup in syringomyelia may be caused by:
- Birth defects (especially "chiari malformation," in which part of the brain pushes down onto the spinal cord at the base of the skull).
- Spinal cord trauma
- Tumors of the spinal cord
The fluid-filled cavity usually begins in the neck area. It expands slowly, putting pressure on the spinal cord and slowly causing damage.
There may be no symptoms, or symptoms may include:
- Loss of muscle mass (wasting , atrophy)
- , loss of ability to use arms or legsMuscle function loss
- or decreased feeling
- Pain down the arms, neck, or into the middle back or legs
- (decreased muscle strength) in the arms or legsWeakness
Other symptoms that may occur with this disease:
Signs and tests
A nervous system (neurologic) examination may show a loss of feeling or movement caused by pressure on the spinal cord.
Other tests that may be done include:
The goals of treatment are to stop the spinal cord damage from getting worse and to improve function.
Surgery to relieve pressure in the spinal cord may be needed. Physical therapy may be needed to improve muscle function.
The health care provider may need to drain the fluid buildup. See: Ventriculoperitoneal shunting
Without treatment, the disorder gets worse very slowly. Over time it will cause severe disability.
Surgery usually stops the condition from getting worse. About 50% of people will have improvements in nervous system function after surgery.
Without treatment, the condition will lead to:
- Loss of nervous system function
- Permanent disability
Possible complications of surgery include:
- Other complications of surgery
Calling your health care provider
Call your health care provider if you have symptoms of syringomyelia.
There is no known way to prevent this condition, other than avoiding injuries to the spinal cord. Getting treated right away slows the disorder from getting worse.
Rekate HL. Spinal cord disorders. In: Kliegman RM, Stanton BF, St. Geme J, Schor N, Behrman RE, eds. . 19th ed. Philadelphia, Pa: Saunders Elsevier; 2011:chap 598.