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Acute Disseminated Encephalomyelitis (ADEM)

Also Known As: ADEM, Post-infectious encephalomyelitis, Immune-mediated demyelinating encephalitis
System: Nervous System
Autoantibodies:
  • No specific autoantibody is diagnostic

  • In some cases, anti-MOG antibodies may be found (linked to recurrent forms)

Primary Organ or Body Part Affected: Brain and spinal cord (central nervous system)
Acceptance as Autoimmune: Confirmed
Acute Disseminated Encephalomyelitis

What is Acute Disseminated Encephalomyelitis (ADEM)?

Acute Disseminated Encephalomyelitis (ADEM) is a rare autoimmune condition that causes sudden inflammation in the brain and spinal cord. It typically follows a viral or bacterial infection (or sometimes a vaccination), and leads to damage of the protective myelin covering on nerve fibers, which disrupts nerve signals.

ADEM is more common in children and young adults, and usually occurs only once (unlike multiple sclerosis, which is recurrent).

What are the signs and symptoms of Acute Disseminated Encephalomyelitis (ADEM)?

  • Sudden fever, headache, and confusion

  • Drowsiness or lethargy

  • Seizures (in some cases)

  • Weakness or numbness (often on one side)

  • Vision problems (blurred vision, eye pain, or double vision)

  • Balance issues or trouble walking

  • Speech difficulties

  • Coma (in severe cases)

Symptoms often develop rapidly over a few days.

What are the causes of Acute Disseminated Encephalomyelitis (ADEM)?

ADEM is believed to be triggered by an immune system overreaction, usually after:

  • Viral infections (e.g., measles, flu, COVID-19, Epstein-Barr)

  • Bacterial infections (rarely)

  • Vaccinations (very rare, e.g., rabies, measles, influenza)

The immune system, in fighting the infection, mistakenly attacks myelin in the central nervous system.

Diagnosis

There’s no single test for ADEM, so doctors rely on:

  • MRI scans – to show inflammation and demyelination in the brain/spinal cord

  • Lumbar puncture (spinal tap) – to check cerebrospinal fluid for inflammation

  • Blood tests – to rule out infections or other autoimmune diseases

  • Sometimes EEG (to detect abnormal brain activity)

Doctors also rule out other conditions like multiple sclerosis or autoimmune encephalitis.

Treatment

  • High-dose corticosteroids (like IV methylprednisolone) are the first line of treatment to reduce inflammation

  • If steroids don’t help:

    • IVIG (intravenous immunoglobulin)

    • Plasmapheresis (plasma exchange)

  • Supportive care (rehab, physical therapy, seizure control)

Prognosis

  • Most people recover fully, especially with early treatment

  • Some may have lingering symptoms (fatigue, concentration issues, or weakness)

  • Rarely, ADEM can be fatal or evolve into multiphasic ADEM or MS

Prognosis is generally better in children than in adults.

Prevalence

  • Estimated 0.4 to 0.8 per 100,000 people per year

  • More common in children under age 10

  • Slightly more common in boys

Citations

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