Progressive multifocal leukoencephalopathy

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| Progressive multifocal leukoencephalopathy | |
|---|---|
| |
| Synonyms | N/A |
| Pronounce | N/A |
| Specialty | N/A |
| Symptoms | Clumsiness, progressive weakness, visual changes, speech disturbances |
| Complications | Severe neurological disability, death |
| Onset | Gradual |
| Duration | Chronic |
| Types | N/A |
| Causes | JC virus infection |
| Risks | Immunosuppression, HIV/AIDS, multiple sclerosis treatment |
| Diagnosis | MRI, PCR for JC virus in cerebrospinal fluid |
| Differential diagnosis | Multiple sclerosis, HIV-associated neurocognitive disorder, CNS lymphoma |
| Prevention | N/A |
| Treatment | Immune reconstitution, antiretroviral therapy |
| Medication | N/A |
| Prognosis | Poor, often fatal |
| Frequency | Rare |
| Deaths | N/A |
Alternate names[edit]
Leukoencephalopathy, progressive multifocal; PML
Definition[edit]
Progressive multifocal leukoencephalopathy (PML) is a neurological disorder that damages the myelin that covers and protects nerves in the white matter of the brain.

Cause[edit]
The John Cunningham virus, or JC virus (JCV) causes PML. JC virus is also known as human polyomavirus 2. By age 10, most people have been infected with this virus though it hardly ever causes symptoms.
Risk factors[edit]
But people with a weakened immune system are at risk of developing PML. Causes of a weakened immune system include:
- HIV/AIDS (less common cause of PML now because of better management of HIV/AIDS).
- Certain medicines that suppress the immune system called monoclonal antibodies. Such medicines may be used to prevent organ transplant rejection or to treat multiple sclerosis, rheumatoid arthritis and other autoimmune disorders, and related conditions.
- Cancers, such as leukemia and Hodgkin lymphoma.
Signs and symptoms[edit]
Symptoms may include any of the following:
- Loss of coordination, clumsiness
- Loss of language ability (aphasia)
- Memory loss
- Vision problems
- Weakness of the legs and arms that gets worse
- Personality changes
Diagnosis[edit]
Tests may include:
- Brain biopsy (in rare cases)
- Cerebrospinal fluid test for the JCV
- CT scan of the brain
- Electroencephalogram (EEG)
- MRI of the brain
Treatment[edit]
- Currently, the best available therapy is reversal of the immune-deficient state, since there are no effective drugs that block virus infection without toxicity.
- Reversal may be achieved by using plasma exchange to accelerate the removal of the therapeutic agents that put patients at risk for PML.
- In the case of HIV-associated PML, immediately beginning anti-retroviral therapy will benefit most individuals.
- Several new drugs that laboratory tests found effective against infection are being used in PML patients with special permission of the U.S. Food and Drug Administration.
- Hexadecyloxypropyl-Cidofovir (CMX001) is currently being studied as a treatment option for JVC because of its ability to suppress JVC by inhibiting viral DNA replication.
Prognosis[edit]
- In general, PML has a mortality rate of 30-50 percent in the first few months following diagnosis but depends on the severity of the underlying disease and treatment received.
- Those who survive PML can be left with severe neurological disabilities.
| Infectious diseases – viral systemic diseases | ||||||||||
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| Diseases of the nervous system, primarily CNS (G04–G47, 323–349) | ||||||||||||||||||||
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NIH genetic and rare disease info[edit]
Progressive multifocal leukoencephalopathy is a rare disease.
| Rare and genetic diseases | ||||||
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Rare diseases - Progressive multifocal leukoencephalopathy
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