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Neoplastic spinal cord compression (Chap. 20. Spinal Cord Compression): Most are epidural in origin, resulting from metastases to the adjacent spinal bones (Fig. 188-2) (see Chap. 20. Spinal Cord Compression). Almost any tumor can be responsible: breast, lung, prostate, kidney, lymphoma, and myeloma most frequent. Thoracic cord most commonly involved. Initial symptom is usually back pain, worse when recumbent, with local tenderness preceding other symptoms by many weeks. Spinal cord compression due to metastases is a medical emergency; in general, therapy will not reverse paralysis of >48 h duration.

Spinal epidural abscess: Triad of fever, localized midline dorsal spine or neck pain, and progressive limb weakness; once neurologic signs appear, cord compression rapidly progresses.

Spinal epidural hematoma: Presents as acute focal or radicular pain followed by variable signs of a spinal cord or conus medullaris disorder.

Acute disk herniation: Cervical and thoracic disk herniations are less common than lumbar.

Spinal cord infarction: Anterior spinal artery infarction produces paraplegia or quadriplegia, sensory loss affecting pain/temperature but sparing vibration/position sensation (supplied by posterior spinal arteries), and loss of sphincter control. Onset sudden or progressive, evolving over minutes or a few hours. Associated conditions: aortic atherosclerosis, dissecting aortic aneurysm, vertebral artery occlusion or dissection in the neck, aortic surgery, or profound hypotension. Therapy is directed at the predisposing condition. Lumbar drainage of spinal fluid is sometimes used prophylactically during aortic surgery but has not been studied systematically.

Immune-mediated myelopathies: Acute transverse myelopathy (ATM) occurs in 1% of pts with SLE; associated with antiphospholipid antibodies. Sjögren's and Behçet's syndromes, mixed connective tissue disease, and p-ANCA vasculitis are other causes. Sarcoid can produce ATM with large edematous swelling of the spinal cord. Demyelinating diseases, either neuromyelitis optica (NMO) or multiple sclerosis (MS), also can present as ATM; glucocorticoids, consisting of IV methylprednisolone followed by oral prednisone, are indicated for moderate to severe symptoms and refractory cases may respond to plasma exchange (Chap. 190. Multiple Sclerosis). Treatment with azathioprine, mycophenolate mofetil, or rituximab may protect against relapses in NMO. Other cases of ATM are idiopathic.

Infectious myelopathies: Herpes zoster is the most common viral agent, but herpes simplex virus types 1 and 2, EBV, CMV, and rabies virus are also well described; in cases of suspected viral myelitis, antivirals may be appropriately started pending laboratory confirmation. A number of enteroviruses and flaviviruses (e.g., West Nile virus) can cause a polio-like syndrome. Bacterial and mycobacterial causes are less common. Schistosomiasis is an important cause worldwide.

Outline

Section 14. Neurology