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Induction and Diverse Assessment Indicators of Experimental Autoimmune Encephalomyelitis
Published on: September 9, 2022
Acute disseminated encephalomyelitis: a report of six cases
G S T Thomas1, I H M I Hussain
1Paediatric Neurology Clinic, Penang Hospital, Jalan Residensi, 10990 Penang.
Insights
Acute Disseminated Encephalomyelitis (ADEM) in children presents with diverse symptoms like fever and seizures. Early treatment with methylprednisolone or immunoglobulins appears crucial for better outcomes, while untreated cases show severe disability.
Area of Science:
- Pediatric Neurology
- Neuroimmunology
- Central Nervous System Disorders
Background:
- Acute Disseminated Encephalomyelitis (ADEM) is an immune-mediated demyelinating disease affecting the central nervous system.
- Understanding ADEM's clinical spectrum and neuroimaging findings is crucial for timely diagnosis and management in children.
Observation:
- A study observed six pediatric cases of ADEM over two years.
- Common symptoms included fever, seizures, ataxia, focal neurological deficits, and mood lability.
- Neuroimaging revealed characteristic white matter and thalamic hyperintensities on MRI.
Findings:
- Three children experienced a prodromal illness; two presented with status epilepticus.
- One child had multiphasic ADEM, experiencing three episodes.
- Treatment with methylprednisolone or immunoglobulins correlated with positive outcomes, while one untreated child had severe disability.
Implications:
- Prompt diagnosis and treatment of ADEM in children are vital for improving neurological outcomes.
- The study highlights the potential benefits of immunomodulatory therapies like methylprednisolone and immunoglobulins.
- Further research into ADEM's pathogenesis and optimal treatment strategies is warranted.
Abstract:
Six children with Acute Disseminated Encephalomyelitis (ADEM) were seen at the Penang Hospital over a two year period (July 1999-June 2001). Diagnosis was based upon typical clinical features and characteristic findings on neuroimaging. Cerebrospinal fluid examination and other investigations were done, where appropriate, to rule out other causes of central nervous system disease. Three children had a prodromal illness. The most common presenting symptoms were fever, seizures, ataxia, focal neurological deficits and labile mood. Two children presented with status epilepticus. All children had an abnormal neurological examination. Brain magnetic resonance imaging revealed hyperintense signals on T2-weighted and FLAIR sequences in the subcortical and deep white matter regions of the frontal, parietal, and temporal lobes, as well as in the thalami, cerebellum and brainstem. One child had multiphasic disseminated encephalomyelitis (three episodes). The child with multiphasic disease had only one treated episode, and has suffered mild disability. Three children were treated with either methylprednisolone or immunoglobulins, and remain well. One child received both treatments but expired as a result of severe gastrointestinal bleeding from the use of methylprednisolone. The child who was not treated has severe disability.
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