Abstract | BACKGROUND: Some pediatric patients with inflammatory demyelinating central nervous system disorders cannot be classified under any of the established disease entities, making their treatment and prognosis difficult. OBJECTIVE: METHODS: RESULTS: We describe seven patients with a median follow-up of six years (five females, two males) who presented at a median age of 6 years (range 4-8 years) with monophasic (n = 4) or recurrent ADEM (two to four attacks) followed by monophasic (n = 3) or recurrent ON (two to nine attacks). Cranial magnetic resonance imaging (MRI) was typical for ADEM (n = 6) with complete or almost complete resolution of lesions on follow-up. Cerebrospinal (CSF) studies at the time of ADEM showed a pleocytosis in six patients and were negative for oligoclonal bands (OCBs) in all. In all patients high titers for serum anti-MOG antibodies were detected. CONCLUSION: ADEM followed by ON is a rare but distinct clinical phenotype among pediatric patients. Further studies are needed to allow recommendations on treatment or prognosis.
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Authors | Peter Huppke, Kevin Rostasy, Michael Karenfort, Brenda Huppke, Rainer Seidl, Steffen Leiz, Markus Reindl, Jutta Gärtner |
Journal | Multiple sclerosis (Houndmills, Basingstoke, England)
(Mult Scler)
Vol. 19
Issue 7
Pg. 941-6
(Jun 2013)
ISSN: 1477-0970 [Electronic] England |
PMID | 23128668
(Publication Type: Journal Article)
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Topics |
- Child
- Child, Preschool
- Encephalomyelitis, Acute Disseminated
(complications, pathology, physiopathology)
- Female
- Humans
- Magnetic Resonance Imaging
- Male
- Optic Neuritis
(complications, pathology, physiopathology)
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