Skip to main content

Obliterating intracranial vasculopathy mimicking multiple sclerosis

Buy Article:

$51.00 plus tax (Refund Policy)

Abstract:

Boentert M, Kraus J, Kloska S, Dittrich R, Nabavi DG, Niederstadt T, Ringelstein EB, Kiefer R. Obliterating intracranial vasculopathy mimicking multiple sclerosis.

Acta Neurol Scand 2009: 120: 68–71.

© 2008 The Authors Journal compilation © 2008 Blackwell Munksgaard. Background – 

The first ever diagnosis of multiple sclerosis (MS) requires consideration of both diagnostic criteria and differential diagnosis. Clinicians are particularly challenged by rare conditions which may mimic MS symptoms and relapses. Case report – 

We report the case of a young female patient who presented with relapsing left hemispheric symptoms that were highly suspicious of MS but were caused by an idiopathic occlusive angiopathy of the circle of Willis. Conclusion – 

Occlusive disease of the great cerebral arteries in young patients is a rare but important differential diagnosis of MS. It has to be considered in patients presenting with the first symptoms suspicious of MS as substantial treatment consequences will arise.

Keywords: diagnostic criteria; moyamoya; multiple sclerosis; stroke; vasculopathy

Document Type: Research Article

DOI: https://doi.org/10.1111/j.1600-0404.2008.01121.x

Affiliations: 1: Department of Neurology, University Hospital of Münster, Münster, Germany 2: Department of Clinical Radiology, University Hospital of Münster, Münster, Germany

Publication date: 2009-07-01

  • Access Key
  • Free ContentFree content
  • Partial Free ContentPartial Free content
  • New ContentNew content
  • Open Access ContentOpen access content
  • Partial Open Access ContentPartial Open access content
  • Subscribed ContentSubscribed content
  • Partial Subscribed ContentPartial Subscribed content
  • Free Trial ContentFree trial content
Cookie Policy
X
Cookie Policy
Ingenta Connect website makes use of cookies so as to keep track of data that you have filled in. I am Happy with this Find out more