Symptoms of Cord Compression Syndrome
The primary symptoms of cord compression syndrome include pain (local and/or radicular) in 90% of patients, weakness, sensory disturbance, and sphincter dysfunction, with up to 50% of patients being unable to walk at presentation. 1
Clinical Presentation
Pain Characteristics
- Back pain (local or radicular) occurs in 88-90% of patients 1
- Pain may be:
- Dull and aching
- Sharp, lancinating, or electrical
- Dysesthetic in character
- Pain may be aggravated by flexion and extension of the spine or by walking/running
- In older teenagers and adults, pain may radiate into the groin, genitals, and/or perianal region 1
Motor Symptoms
- Progressive weakness, typically worse in upper extremities than lower extremities in central cord syndrome 2
- Difficulty walking or running
- Muscle atrophy (thinning of calf muscles)
- Decreased athletic performance
- Progressive difficulty with ambulation 1
Sensory Abnormalities
- Sensory deficits typically start distally in the leg and become more proximal over time
- "Suspended" sensory loss may occur with preserved sensation both above and below the affected area 1
- Prominent sensory complaints in the hands (especially in central cord syndrome) 2
- Paresthesias and dysesthesias
Autonomic Dysfunction
- Bladder dysfunction (44% of patients) 3
- Urinary urgency and/or incontinence
- Urinary tract infections
- Dribbling urinary stream
- Incomplete emptying
- Inability to void
- Bowel dysfunction
- Fecal urgency and/or incontinence
- Constipation (34% of patients) 3
Other Signs and Symptoms
- Orthopedic deformities:
- Progressive scoliosis
- Exaggerated lumbosacral lordosis
- Foot deformities
- In long-standing cases:
- Thin, shiny, hairless skin on legs and feet due to autonomic changes
- Areas of skin breakdown and chronic discoloration 1
Progression and Warning Signs
- Symptoms typically progress if untreated, leading to relentless and progressive neurological deterioration 1
- Sudden appearance of new pain and/or neurologic deficits after back stretching (e.g., during childbirth, falls onto buttocks, vigorous sports) may indicate acute cord compression 1
- Patients with paralysis either at presentation or after treatment have a much shorter life expectancy than ambulatory patients 1
Diagnostic Considerations
- MRI with contrast enhancement is the gold standard for diagnosis with sensitivity ranging from 0.44 to 0.93 and specificity from 0.90 to 0.98 4
- CT myelography may be used as an alternative when MRI is contraindicated 4
- Back pain alone is not predictive of spinal cord compression, but progressive neurological symptoms warrant urgent imaging 4
Clinical Pitfalls
- Delayed diagnosis can lead to irreversible neurological deficits 4
- Symptoms may be misdiagnosed as other conditions (e.g., Charcot-Marie-Tooth syndrome) 1
- In children and teenagers, subtle abnormalities may be present from early childhood before more severe symptoms develop 1
- Patients with a history of cancer who develop new back pain should be evaluated urgently for possible cord compression 1
Early recognition and prompt treatment of cord compression syndrome are essential to prevent permanent neurological damage and improve outcomes, with pretreatment ambulatory status being the most important prognostic factor 4.