Infections of the nervous system II

Published on 10/04/2015 by admin

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Last modified 22/04/2025

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Infections of the nervous system II

Spinal infections

Specific infections of the spinal cord are caused by viruses such as HTLV-1, polio, herpes zoster, herpes simplex and Epstein–Barr, bacterial and other infections including syphilis (see below) and Lyme disease. Infection can also spread from the spine. The spinal cord and cauda equina may also be affected by meningitic processes described previously and in association with meningoencephalitis.

HTLV-1 is a retrovirus. It is common in the West Indies, Africa and southern USA and in immigrants from these areas. Myelopathy occurs in a small proportion of seropositive patients (2–5%) and presents as a slowly progressive weakness and stiffness in the legs with sensory symptoms and prominent bladder symptoms. The arms are rarely affected. Oligoclonal bands are positive in the CSF. The main differential diagnosis is with multiple sclerosis. Treatment is symptomatic.

Poliomyelitis is now extremely rare. It can lead to a myelitis and leave significant neurological deficit (p. 109).

Other viruses, particularly from the herpes group, can produce a transverse myelitis, though this is usually in the immunocompromised.

Pyogenic infection in the vertebral body or in the epidural space can lead to an epidural abscess (Fig. 1), producing back pain often associated with fever. This is followed by radicular pain and then symptoms and signs of spinal cord or cauda equina involvement. If this diagnosis is suspected then urgent investigation with spinal MRI is needed, as early drainage of the abscess and high-dose antibiotics is the only hope of reversing this process. A similar, if slower, onset is associated with tuberculous epidural abscess. Treatment of this is primarily antituberculous therapy, though in some patients surgery is needed.

Syphilis

Syphilis used to be the great mimic in neurology and syphilis serology was performed on all patients with neurological disease. Neurosyphilis is now rare. Pathologically, neurosyphilis occurs because of a chronic syphilitic meningitis and an endarteritis. These result in a large number of neurological abnormalities that can be categorized into four neurological syndromes, most of which occur years after the original infection:

The diagnosis of syphilis is in two phases. Blood serology (TPHA, VDRL and FTA) identifies patients with current or prior infection. CSF examination is used to determine the activity of infection, measuring cell count, protein and VDRL titre. Treatment is with prolonged (21 days) supervised courses of intramuscular penicillin.

HIV infections and AIDS

Neurological complications can occur at any stage of HIV infection. At seroconversion, Guillain–Barré syndrome and facial weakness have been documented. During the asymptomatic phase of HIV infection, chronic demyelinating neuropathies may occur.

Most neurological problems in HIV infection occur as the patient develops significant immunosuppression. Opportunistic infections, tumours, specific neurological problems associated with HIV and neurological complications of the treatment of HIV infection then occur. Different levels of the nervous system are affected and are summarized in Table 1.

Toxoplasmosis

This presents with a focal neurological deficit, headache or seizures, usually developing over a few weeks (Fig. 2). Brain scanning reveals single or multiple ring-enhancing masses with oedema. As this is the most likely diagnosis in this setting, a trial of anti-toxoplasma treatment is given. Further investigation is considered if this fails. The most common differential diagnosis is primary CNS lymphoma. This can be treated with radiotherapy but the response and prognosis are poor.