2004
DOI: 10.1097/01.inf.0000133048.75452.dd
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Acute Disseminated Encephalomyelitis in Childhood: Epidemiologic, Clinical and Laboratory Features

Abstract: ADEM is a potentially severe demyelinating disorder likely to be increasingly diagnosed as more magnetic resonance imaging studies are performed on patients with acute encephalopathy. Further characterization of the central nervous system inflammatory response will be needed to understand ADEM pathogenesis, to improve diagnostic and treatment strategies and to distinguish ADEM from MS.

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Cited by 357 publications
(341 citation statements)
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References 70 publications
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“…While the majority of ADEM patients experience a monophasic disease course with partial or complete recovery, some have a recurrence of the same symptoms and lesion location more than 3 months following the initial event (recurrent ADEM) or experience new lesions and symptoms (multiphasic ADEM) (Krupp et al, 2007). A minority of individuals with ADEM can later develop MS, although the reported frequency of this occurrence is highly variable (0-28%) (Dale et al, 2000;Leake et al, 2004;Mikaeloff et al, 2004Mikaeloff et al, , 2007Tenembaum et al, 2002), requires many years of follow-up, and is dependent on the criteria used to define MS. For instance, Poser's criteria (Poser et al, 1983) would consider multiphasic ADEM as MS, as both are a recurring demyelinating events separated in space and time. The overlapping symptoms and lack of specific biomarkers can cause difficulties in distinguishing between MS and ADEM, especially in pediatric populations (Belman et al, 2007;Krupp et al, 2007;Wingerchuk, 2003).…”
Section: Ms and Related Inflammatory Demyelinating Cns Diseasesmentioning
confidence: 99%
“…While the majority of ADEM patients experience a monophasic disease course with partial or complete recovery, some have a recurrence of the same symptoms and lesion location more than 3 months following the initial event (recurrent ADEM) or experience new lesions and symptoms (multiphasic ADEM) (Krupp et al, 2007). A minority of individuals with ADEM can later develop MS, although the reported frequency of this occurrence is highly variable (0-28%) (Dale et al, 2000;Leake et al, 2004;Mikaeloff et al, 2004Mikaeloff et al, , 2007Tenembaum et al, 2002), requires many years of follow-up, and is dependent on the criteria used to define MS. For instance, Poser's criteria (Poser et al, 1983) would consider multiphasic ADEM as MS, as both are a recurring demyelinating events separated in space and time. The overlapping symptoms and lack of specific biomarkers can cause difficulties in distinguishing between MS and ADEM, especially in pediatric populations (Belman et al, 2007;Krupp et al, 2007;Wingerchuk, 2003).…”
Section: Ms and Related Inflammatory Demyelinating Cns Diseasesmentioning
confidence: 99%
“…ADEM is most common in children, with an incidence of approximately 4 per million of the population who are <20 years of age (and even higher among younger children) [53]. Adults can develop ADEM, but it is uncommon.…”
Section: Ademmentioning
confidence: 99%
“…Patolojik olarak perivasküler enflamasyon, ödem ve demiyelinizasyonla belirgindir. Klinik olarak, hastal›¤a özgül olmayan sistemik belirti ve bulgularla s›n›rl› kalabilir ya da h›zl› geliflen fokal ya da mültifokal nörolojik ifllev bozuklu¤u görülebilir (3). Tan›, en iyi manyetik rezonans görüntüleme (MRG) ile yap›-l›r (4).…”
Section: Giriflunclassified