Progressive Multifocal Leukoencephalopathy (PML)
(See also Overview of Brain Infections.)
Progressive multifocal leukoencephalopathy is a rare infection of the brain that is caused by the JC (John Cunningham) virus.
People with a weakened immune system are most likely to get the disorder.
People may become clumsy, have trouble speaking, and become partially blind, and mental function declines rapidly.
Death usually occurs within 9 months.
Imaging of the head and a spinal tap are done.
Treating the disorder that weakened the immune system may help.
Progressive multifocal leukoencephalopathy results from infection by the JC virus (which is not related to Creutzfeldt-Jakob disease). The JC virus is often acquired during childhood. Most adults have been infected with the JC virus but do not develop the disorder.
The virus appears to remain inactive until something (such as a weakened immune system) allows it to be reactivated and start to multiply. Thus, the disorder affects mainly people whose immune system has been weakened by a disorder (such as leukemia, lymphoma, or AIDS) or by drugs that suppress the immune system (immunosuppressants) or that modify the immune system (immunomodulators). Such drugs include those used to prevent rejection of transplanted organs or to treat cancer or autoimmune disorders, such as systemic lupus erythematosus (lupus) or multiple sclerosis. Monoclonal antibodies such as natalizumab and rituximab are examples of these drugs.
The JC virus appears to cause no symptoms until it is reactivated.
Symptoms of progressive multifocal leukoencephalopathy may begin gradually and usually worsen progressively. They vary depending on which part of the brain is infected. In about two of three people, mental function declines rapidly and progressively, causing dementia. Speaking becomes increasingly difficult. People may become partially blind. Walking may become difficult. Rarely, headaches and seizures occur, mainly in people with AIDS.
Death is common within 1 to 9 months of when symptoms start, but a few people survive longer (about 2 years).
Progressively worsening symptoms in people with a weakened immune system suggest progressive multifocal leukoencephalopathy.
Magnetic resonance imaging (MRI) of the head is done. It can usually detect abnormalities that suggest the diagnosis.
A spinal tap (lumbar puncture) is done to obtain a sample of cerebrospinal fluid (the fluid that flows through the tissues that cover the brain and spinal cord). The polymerase chain reaction (PCR) technique, which produces many copies of a gene, is used to detect the JC virus's DNA in the cerebrospinal fluid.
Sometimes the diagnosis is not confirmed until after people have died, when brain tissue can be examined.
No treatment for progressive multifocal leukoencephalopathy has proved effective. However, if the disorder that has weakened the immune system is treated, people survive longer. For example, if the cause is AIDS, antiretroviral therapy is used.
If people are taking immunosuppressants or other drugs that affect the immune system (such as natalizumab), stopping the drugs may cause progressive multifocal leukoencephalopathy to subside. Sometimes plasma exchange is used to remove the drug from the blood, particularly when the drug is natalizumab (used to treat multiple sclerosis).
People who are treated with antiretroviral therapy or who stop taking immunosuppressants may develop immune reconstitution inflammatory syndrome (IRIS). In this disorder, the recovering immune system launches an intense attack against the JC virus, which can make symptoms temporarily worse. Corticosteroids may help relieve symptoms.
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