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Acute Disseminated Encephalomyelitis

Get the facts on Acute Disseminated Encephalomyelitis treatment, diagnosis, staging, causes, types, symptoms. Information and current news about clinical trials and trial-related data, Acute Disseminated Encephalomyelitis prevention, screening, research, statistics and other Acute Disseminated Encephalomyelitis related topics. We answer all your qestions about Acute Disseminated Encephalomyelitis.

Question: What is Acute disseminated encephalomyelitis (ADEM)?

Answer: Acute disseminated encephalomyelitis (ADE) is a neurological disorder involving inflammation of the brain and spinal cord. A hallmark of the disorder is damage to the myelin sheath that surrounds the nerve fibers in the brain, which results in the inflammation. Description Acute disseminating encephalomyelitis was first described in the mid-eighteenth century. The English physician who first described the disorder noted its association with people who had recently recovered from smallpox. Symptoms often develop without warning. As well, mental disorientation can occur. The disorder is also known as postinfectious encephalomyelitis and immune-mediated encephalomyelitis. The nerve demyelination that occurs in ADE also occurs in multiple sclerosis. However, the two maladies differ in that multiple sclerosis is long lasting and can recur over time, while ADE has a monophasic course, meaning that once it is over, further attacks rarely occur. Demographics ADE can occur in both children and adults, although it occurs more commonly in children. ADE is not rare, accounting for approximately 30% of all cases of encephalitis (brain inflammation). Causes and symptoms Acute disseminating encephalomyelitis can occur as a consequence of a bacterial or viral infection (including HIV), following recovery from infection with the malarial protozoan, or as a side effect of vaccination or another inoculation. ADE is usually a consequence of a viral illness, and occurs most often after measles, followed by rubella, chicken pox, Epstein-Barr, mumps and pertussis (whooping cough). Typically, symptoms appear two to three weeks after the precipitating infection or immunization. Alternatively, ADE may develop with no known associations. Despite the different causes, the symptoms that develop are similar. A number of non-specific symptoms, which vary from one person to another, include headache, stiff neck, fever, vomiting, and weight loss. These symptoms are quickly followed by lethargic behavior, seizures, hallucinations, sight difficulties, and even coma. Paralysis can occur in an arm or leg (monoparesis) or along an entire side of the body (hemiplegia). Treatment Corticosteroid medication is often prescribed in order to lessen the nerve inflammation. Use of high doses of steroids can often produce a rapid diminishing of the symptoms. Other kinds of treatment depend on the nature of the symptoms that develop. I hope this is of use to you best wishes and good luck


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