Cited by 511Multiple Sclerosis Research StudiesPeripheral Neuropathies and DisordersPolyomavirus and related diseases

Acute disseminated encephalomyelitis: A follow-up study of 40 adult patients

Schwarz, S., Mohr, A., Knauth, M., Wildemann, B., Storch–Hagenlocher, B.·2001·Neurology

Abstract

Objectives To describe the clinical, CSF, and radiologic findings and long-term follow-up in a cohort of patients with acute disseminated encephalomyelitis (ADEM), and to determine possible prognostic factors for progression to MS. Methods Forty adults (28 women, mean age 33.5 years) diagnosed with ADEM were analyzed. Clinical symptoms, cranial MRI and CSF findings, and the response to a standardized treatment during the acute phase of the disease were analyzed by chart review. The final diagnosis of ADEM or clinically definite MS was established upon follow-up examination after 8 to 137 months. The patients with ADEM and MS were compared to detect differences between the two groups. Results Fifteen patients had a preceding infection (n = 14) or immunization (n = 1). The most frequent clinical signs were motor deficit (80%), followed by sensory deficits, brainstem signs, and ataxia. CSF findings were highly variable; normal results were present in 20% of patients. Oligoclonal bands were positive in 65% of patients. Ninety-five percent of all patients improved during the acute phase of the disease. Upon follow-up, 14 patients had developed clinically definite MS. Of the 26 patients with the final diagnosis of ADEM, two patients had died, nine had minor deficits, three had moderate deficits, and 12 patients had no remaining symptoms. Patients with the final diagnosis of ADEM were older, and more often had a preceding infection, clinical signs of brainstem involvement, a higher…

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Crossref · 10.1212/wnl.56.10.1313

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  • ADEM is almost always monophasic; however, an encephalopathic ADEM-like illness can sometimes be the first presentation of MS in both children and adults and diagnostic criteria for ADEM remain imperfect.

    “ADEM is almost always monophasic; however, an encephalopathic ADEM-like illness can sometimes be the first presentation of MS in both children 32,34 and adults 43 and diagnostic criteria for ADEM remain imperfect.”

    From Diagnosis of multiple sclerosis: progress and challenges (2017) · cites this paper as [43]

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Authors
Schwarz, S., Mohr, A., Knauth, M., Wildemann, B., & Storch–Hagenlocher, B.
Affiliations
  • Heidelberg University (DE)
  • From the Departments of Neurology (Drs. Schwarz, Wildemann, and Storch–Hagenlocher) and Neuroradiology (Drs. Mohr and Knauth), University of Heidelberg, Germany.
Venue
Neurology
Published
2001-05-22
Volume
56
Issue
10
Pages
1313-1318
ISSN
  • 0028-3878 (ISSN-L)
  • 1526-632X
OpenAlex
W2011257132
Cited by
511
References
0
Citations by year
2026: 5 · 2025: 11 · 2024: 12 · 2023: 13 · 2022: 18 · 2021: 23 · 2020: 18 · 2019: 22 · 2018: 14 · 2017: 18 · 2016: 18 · 2015: 18 · 2014: 23 · 2013: 20 · 2012: 27
FWCI
13.81
Type
journal article
Language
en
Open access
closed
Locations
  • Neurology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
  • Health Sciences › Medicine › Neurology › Peripheral Neuropathies and Disorders
  • Health Sciences › Medicine › Oncology › Polyomavirus and related diseases
Keywords
acute disseminated encephalomyelitis, multiple sclerosis, long-term follow-up, prognostic factors, oligoclonal bands, brainstem involvement, infratentorial lesions, preceding infection, immunization, diagnostic criteria, adult patients
MeSH terms
Adult, Anti-Inflammatory Agents, Brain, Cyclophosphamide, Diagnosis, Differential, Encephalomyelitis, Acute Disseminated, Female, Follow-Up Studies, Humans, Immunosuppressive Agents, Magnetic Resonance Imaging, Male, Methylprednisolone, Middle Aged, Multiple Sclerosis, Prognosis, Tomography, X-Ray Computed, Cohort Studies, Treatment Outcome

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