Spinal Cord Compression Flashcards
Why is prompt Dx of spinal cord compression essential?
Rapidly evolving spinal cord compression (hours to days) is a NEUROSURGICAL EMERGENCY which should be managed as soon as possible to avoid permanent neurological disability
Recognise the appearance of extradural, intradural/extramedullary and intramedullary lesions which may compress the spinal cord and cauda equina. Which is the most common?
What are the 5 most common categories of causes of spinal cord compression?
Tumour (primary or metastatic)
Degenerative
Infection
Haematoma
Developmental
List 3 degenerative causes of spinal cord compression
Disc prolapse
OP
Spondylosis
What anatomical features are possible sites of infection which may cause spinal cord compression?
Vertebral body
Disc space
Extradural
Intradural
Give 3 causes of spinal haematoma which may result in spinal cord compression
Spontaneous
Trauma
AVM
List 3 developmental abnormalities which may result in spinal cord compression
Syrinx
AVM
Arachnoid cyst
What is a syrinx?
Syringomyelia is the formation of a fluid-filled cyst (syrinx) within the spinal cord
As the cyst grows, it may compress the spinal cord
Causes include trauma, infection and congenital brain defects
What is an arachnoid cyst?
Cerebrospinal fluid-filled sacs covered by arachnoid cells and collagen that are located between the brain or spinal cord and the arachnoid membrane
Primary arachnoid cysts are present at birth and are the result of developmental abnormalities; secondary arachnoid cysts are not as common as primary cysts and develop as a result of head injury, meningitis, or tumors, or as a complication of brain surgery
Majority form in the middle cranial fossa (spinal cord cysts are less common)
Give 3 examples of extradural causes of spinal cord and cauda equina compression
Metastatic tumour
Abscess
Degenerative spinal disease
Give 3 examples of intradural/extramedullary causes of spinal cord and cauda equina compression
Meningioma
Schwannoma
Myxopapillary ependymoma
Give 2 examples of intramedullary causes of spinal cord and cauda equina compression
Glioma (astrocytoma or ependymoma)
Syrinx
Overview of meningioma (what is it, presentation, Dx, Ix, Mx)
Predominantly benign tumour of the meninges occurring at both cranial and spinal sites; they are occasionally atypical or malignant in nature
Sx: produces symptoms from local mass effect due to compression of neural structures or may present with seizure
Dx: diagnosis confirmed by the characteristic appearance on MRI with and without contrast enhancement
Ix: asymptomatic lesions may be followed up with serial observation
Mx: treatment of symptomatic meningioma is usually surgical resection, although, in some cases, local radiotherapy is used as primary treatment
What is schwanomma?
A schwannoma is a benign nerve sheath tumour composed of Schwann cells, which normally produce the insulating myelin sheath covering peripheral nerves
Less than 1% become malignant, degenerating into a form of cancer known as neurofibrosarcoma
What is myxopapillary ependymoma?
Thought to arise from the ependymal glia of the filum terminale or conus medullaris (at the end of the spinal cord); histologically, they contain papillary elements in a myxoid background, admixed with ependymoma-like cells
What is an ependymoma?
Ependymomas arise from ependymal cells lining the central canal or cell rests along the filum; they are the most common spinal cord tumour overall
What is an astrocytoma?
Astrocytomas (both intracranial and spinal) arise from astrocytic glial cells; spinal cord astrocytomas generally have a lower histologic grade than astrocytomas in the brain
They are the second most common spinal cord tumour overall
If a patient presents with LL neurological disturbance but UL is normal, what does this suggest about the location and level of the lesion?
No cervical spine involvement
What is the most common cause of cauda equina syndrome?
Acute disc prolapse
How might spinal cord compression present differently to cauda equina?
Spinal cord compression can present with UMN signs
In cauda equina syndrome, all signs are consistent with a LMN lesion
What are the two major presenting features of spinal cord compression and cauda equina syndrome? What factors can affect the presentation?
Presentation: pain and neurological deficit
Modified depending on: site of compression, speed of onset, involvement of adjacent nerve roots, cause, and involvement of blood supply of the spinal cord
Mr Verdi, 73, visited his GP complaining of difficulty walking
He could not describe the symptom very well, but thought his legs had been generally weak and stiff; he also noted some trouble with fine movements of his hands
What are these symptoms suggestive of?
Weak and stiff: may suggest UMN lesion
Involvement of hands: suggests cervical spine
Mr Verdi, 73, presents with difficulty walking
Previously well, PHx: OA of knees, occasional low back pain, more recently some neck pain, no surgery, no cancers
Symptoms have been progressively worsening over many months or maybe even years
Walking has been “shuffling” and he feels unable to continue for long distances; he has had a number of falls and feels unsteady
His hands feel numb and he has had trouble with buttoning his shirt and turning the pages of the newspaper
His bladder and bowel function have been normal
O/E: moderate restriction of neck movements due to mild pain and stiffness, shuffling stiff gait, UL power relatively normal but depressed reflexes, light touch sensation in hands diffusely reduced with no clear dermatomal distribution, LL power only mildly reduced but tone elevated and very brisk reflexes, Babinski’s sign positive, light touch sensation in LLs normal but proprioception and vibration reduced
What picture is this?
What anatomical level is the lesion
DDx?
What should Mr Verdi’s GP do next? Ix and Mx?
Mixed picture: UL has LMN pattern, LL has UMN pattern with spastic paraparesis
Hx and Ex suggest a slowly progressive compressive lesion of the cervical spinal cord (a classic “cervical myelopathy”)
In an older patient with neck pain, slow Sx onset, no fever and no Hx of cancer, this is most likely due to degenerative cervical canal stenosis
Main DDx: spinal tumour (primary or metastatic), spinal infection, inflammatory or neurodegeneraive diseases (MS, MND, syringomyelia/syrinx, subacute combined degeneration of the spinal cord)
Ix: baseline bloods, CT scan of cervical spine
Mx: neurosurg referral (who will most likely order an MRI of the cervical spine)
Mr Verdi, 73, presents with difficulty walking and has signs O/E of spinal cord compression
MRI: severe cervical canal stenosis with cord signal change due to disc prolapse, spondylosis and hypertrophy of the ligamentum flavum
Is this an emergency?
No; has a slow progression
Where does degenerative spinal canal stenosis usually occur? What sites produce the most clinically significant presentations?
May occur anywhere along the spinal column
Most clinically significant lesions are in the cervical spine (causing cervical myelopathy due to cord compression) and in the lumbar spine (causing sciatica and neurogenic claudication due to cauda equina compression)
What degenerative changes can contribute to spinal canal stenosis? What factors can contribute to these degenerative changes?
Spondylosis with hypertrophy and osteophytes of the fact joints
Hypertrophy of ligamentum flavum
Bulging or prolapsed intervertebral discs and associated osteophytes
Contributing factors: excessive mobility, often on a background of a congenitally narrow canal
What is the most common cause of spinal cord compression due to degenerative spinal canal stenosis?
Spondylotic spinal myelopathy
What is the effect of surgical intervention on symptoms of a chronically evolving spinal cord compression?
Operation stops the progression of symptoms but does not reverse or improve current symptoms
What is the cause of the neurological symptoms seen in degenerative spinal cord stenosis?
Direct pressure on neural structures
Ischaemia of the neural structures
What pathological changes occur in the spinal cord due to compression and ischaemia of the neural structures?
Degeneration and loss of nerve cells
Spinal cord cavitation
Glial cell proliferation
Demyelination
Wallerian degeneration of tracts above and below the level of compression