Acute fulminant demyelinating disease - A descriptive study of 60 patients
Acute fulminant demyelinating disease - A descriptive study of 60 patients
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DOI:
10.1001/archneur.64.10.1426
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发表时间:
2007-10-01
影响因子:
--
通讯作者:
Vermersch, Patrick
中科院分区:
文献类型:
--
作者:
de Seze, Jerome;Debouverie, Marc;Vermersch, Patrick
Background: Acute demyelinating encephalomyelitis (ADEM) is characterized by a severe inflammatory attack, frequently secondary to infectious events or vaccinations. To date, no clear criteria exist for ADEM, and the risk of subsequent evolution to multiple sclerosis (MS) remains unknown.Objective: To evaluate the risk of evolution to MS after a first episode of ADEM.Design: Observational, retrospective case study.Setting: Thirteen French MS centers.Patients: We retrospectively studied 60 patients with ADEM who were older than 15 years with no history suggestive of an inflammatory event who presented to MS centers from January 1, 1995, through December 31, 2005. We excluded 6 patients with multiphasic ADEM because this is a rare condition and somewhat difficult to classify. After a mean follow-up of 3.1 years (range, 1-10 years), the remaining 54 patients were then classified into 2 groups: monophasic ADEM(ADEM group) (n= 35) and clinically definite MS (MS group) (n= 19).Main Outcome Measures: Clinical, laboratory, magnetic resonance imaging, and follow-up data were evaluated for each group.Results: Patients in the ADEM group more frequently had atypical symptoms of MS ( 26 of 35 [74%]) than patients with MS ( 8 of 19 [42%]) ( P=.02). Oligoclonal bands were more frequently observed in the MS group ( 16 of 19 [84%]) than in the ADEM group ( 7 of 35 [20%]) (P