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Updated: Jul 27, 2026

Induction and Clinical Scoring of Chronic-Relapsing Experimental Autoimmune Encephalomyelitis
Published on: July 4, 2007
[Disseminated acute encephalomyelitis in children. A retrospective study of seven patients]
F A Gómez-Gosálvez1, P Smeyers, F Menor
1Servicio de Pediatría, Hospital Virgen de Los Lirios, Alcoy, Alicante. fagomezgos@coma.es
Insights
Acute disseminated encephalomyelitis (ADEM) is an inflammatory brain disease. This study found that ADEM in children typically resolves within two months with appropriate treatment.
Area of Science:
- Pediatric Neurology
- Neuroimmunology
- Demyelinating Diseases
Background:
- Acute disseminated encephalomyelitis (ADEM) is a rare inflammatory demyelinating disorder of the central nervous system.
- Understanding ADEM's clinical presentation and diagnostic markers is crucial for timely intervention.
Observation:
- This study analyzed seven pediatric cases of ADEM, detailing initial neurological symptoms, diagnostic test results, and treatment outcomes.
- Common initial symptoms included hemiparesis, cerebellar and pyramidal syndromes, altered consciousness, seizures, and cranial nerve palsies.
- Cerebrospinal fluid abnormalities and positive serology for Coxsackie B were noted in some patients, with electrophysiological studies affected in 50%.
Findings:
- Magnetic Resonance Imaging (MRI) revealed multifocal supratentorial white matter lesions consistent with demyelination.
- Patients experienced progressive neurological improvement, with symptom resolution typically occurring within two months.
- Treatment involved acyclovir and corticosteroids, leading to favorable clinical outcomes.
Implications:
- ADEM generally follows a monophasic course with progressive neurological deficits.
- Diagnosis relies on characteristic clinical and neuroimaging findings, particularly MRI.
- The study highlights the effectiveness of prompt treatment and the generally good prognosis for pediatric ADEM, with MRI evidence of lesion resolution correlating with clinical recovery.
Introduction And Objective:
Acute disseminated encephalomyelitis (ADEM) is an inflammatory demyelinating disease of the central nervous system. This study is based on clinical symptoms and diagnostic tests employed.
Patients And Methods:
We describe a seven children series indicating the initial neurologic abnormalities, diagnostic tests, treatments used and clinical-neuroradiological evolution.
Results:
The mean presentation age was 4.1 years. Initial neurologic symptoms were mainly spastic hemi/paraparesis, cerebellous and pyramidal syndrome, consciousness changes, meningeal signs, seizures and cranial nerve palsies. The cerebrospinal fluid was abnormal in four patients with positive serologic tests in two of them (Coxsackie B). Electrophysiological studies were affected in 50%. MRI findings consisted of multifocal supratentorial white matter lesions. Clinical evolution revealed a progressive improvement with resolution after two months. Follow-up was made between six months and five years. The treatment was based on aciclovir and corticosteroids.
Conclusions:
ADEM runs a monophasic course of progressive neurologic abnormalities. Diagnosis is based on suggestive clinical and neuroimaging findings. Generally speaking, MRI showed resolution of multifocal lesions in conjunction with clinical improvement.
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