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Updated: Jun 20, 2026

Induction and Clinical Scoring of Chronic-Relapsing Experimental Autoimmune Encephalomyelitis
Published on: July 4, 2007
[Acute disseminated encephalomyelitis in childhood]
Zoltán Liptai1, Eniko Ujhelyi, Ilona Mihály
1László Kórháza, Gyermekgyógyászati Osztály, 1097 Budapest, Gyáli út 5-7. zoltan.liptai@laszlokorhaz.hu
Insights
This study analyzed acute disseminated encephalomyelitis (ADEM) in children, finding viral triggers in most cases. While outcomes were similar to literature, a higher proportion of identified viruses suggests a stronger etiological link.
Area of Science:
- Pediatric Neurology
- Demyelinating Diseases
- Infectious Diseases
Background:
- Acute disseminated encephalomyelitis (ADEM) is a rare inflammatory demyelinating disorder.
- It is frequently preceded by infections or vaccinations.
Purpose of the Study:
- To systematically analyze clinical, radiological, and microbiological profiles of children with ADEM.
- To compare findings with existing literature data.
Main Methods:
- Retrospective analysis of demographic, infectological, clinical, radiological, laboratory, and virological data.
- Patient data collected from January 1998 to June 2008.
Main Results:
- 19 children diagnosed with ADEM, mean age 6.8 years.
- Viral etiology confirmed or probable in 15/19 patients.
- MRI revealed widespread white and gray matter changes; 17/19 had prodromal illness.
- Treatment included methylprednisolone, plasma exchange, or immunoglobulin; 9 required ventilation.
- Outcomes varied: 2 deaths, 10 recovered without sequelae, 7 with sequelae; 2 developed further demyelinating events.
Conclusions:
- Clinical and radiological findings align with literature.
- A higher proportion of identified triggering viruses in this cohort compared to previous studies.
Background And Purpose:
Acute disseminated encephalomyelitis is a rare inflammatory demyelinating disorder often preceded by infection or vaccination. The purpose of the study was the systematic analysis of clinical, radiological and microbiological profiles of children treated at Szent László Hospital, and the comparison of findings with literature data.
Methods:
Demographic, infectological, clinical, radiological, laboratory and virological data of patients treated and followed-up between 1-Jan-1998 and 30-June-2008 were reviewed and analysed.
Results:
19 children met diagnostic criteria. Their mean age was 6.8 years. A prodromal illness--mostly febrile viral infection, upper respiratory infection or chickenpox--preceded neurological symptoms in 17 patients. All had polysymptomatic encephalopathy, 2 children had spinal symptoms. The cerebrospinal fluid was abnormal in all but one. A viral etiology was definite in 7 and probable in 8 cases. MRI disclosed white matter changes in 18, cortical and deep gray matter in 16, cerebellar in 6, brain stem in 14 and spinal cord changes in 2 cases. Repeat MRI performed mean 4 months later showed complete resolution in 6 and partial resolution in 11 patients. 13 patients received high-dose methylprednisolone, 2 of whom were also treated with plasma exchange and 1 with immunoglobulin. 9 children required mechanical ventilation. 2 patients died, 10 recovered without and 7 with sequelae. 2 patients developed further demyelinating events: multiple sclerosis and multiphasic disseminated encephalomyelitis, respectively.
Conclusion:
Clinical, radiological and follow-up results were similar to those published in literature however, triggering viruses were identified in a larger proportion of cases.
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