Acute disseminated encephalomyelitis

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Alternate names



Acute disseminated encephalomyelitis (ADEM) is a neurological condition characterized by a brief but intense attack of inflammation in the brain and spinal cord. This may lead to damage of the layer of insulation around the nerves (myelin) within affected areas.



  • ADEM is not an inherited condition, and we are not aware of any familial cases (reports of ADEM occurring in more than one family member).
  • However, some people may be more susceptible to having ADEM.
  • Susceptibility is likely due to multiple factors, including complex interactions between genetics, exposure to infections, immunization exposure, and other environmental factors.
  • Because there are no specific genes known to increase a person's risk to have ADEM, there is no "susceptibility" test for children who may be at risk, or for parents concerned that current or future children may be at risk.

Signs and symptoms

  • The symptoms of ADEM appear rapidly, beginning with encephalitis-like symptoms such as fever, fatigue, headache, nausea and vomiting, and in the most severe cases, seizures and coma.
  • ADEM typically damages white matter (brain tissue that takes its name from the white color of myelin), leading to neurological symptoms such as visual loss (due to inflammation of the optic nerve) in one or both eyes, weakness even to the point of paralysis, and difficulty coordinating voluntary muscle movements (such as those used in walking).
  • ADEM is sometimes misdiagnosed as a severe first attack of multiple sclerosis (MS), since the symptoms and the appearance of the white matter injury on brain imaging may be similar.
  • However, ADEM has several features which differentiate it from MS.
  • First, unlike MS patients, persons with ADEM will have rapid onset of fever, a history of recent infection or immunization, and some degree of impairment of consciousness, perhaps even coma; these features are not typically seen in MS.
  • Children are more likely than adults to have ADEM, whereas MS is a rare diagnosis in children.
  • In addition, ADEM usually consists of a single episode or attack of widespread myelin damage, while MS features many attacks over the course of time.


Doctors will often use imaging techniques, such as MRI (magnetic resonance imaging), to search for old and new lesions (areas of damage) on the brain. The presence of older brain lesions on MRI suggest that the condition may be MS rather than ADEM, since MS can cause brain lesions before symptoms become obvious. In rare situations, a brain biopsy may be necessary to differentiate between ADEM and some other diseases that involve inflammation and damage to myelin.



  • Corticosteroid therapy typically helps hasten recovery from most ADEM symptoms.
  • The long-term prognosis for individuals with ADEM is generally favorable.
  • For most individuals, recovery begins within days, and within six months the majority of ADEM patients will have total or near total recoveries.
  • Others may have mild to moderate lifelong impairment ranging from cognitive difficulties, weakness, loss of vision, or numbness.
  • Severe cases of ADEM can be fatal but this is a very rare occurrence.
  • ADEM can recur, usually within months of the initial diagnosis, and is treated by restarting corticosteroids.
  • A small fraction of individuals who are initially diagnosed as having ADEM can go on to develop MS, but there is currently no method or known risk factors to predict whom those individuals will be.

NIH genetic and rare disease info

Acute disseminated encephalomyelitis is a rare disease.

Latest research - Acute disseminated encephalomyelitis

Clinical trials


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