Literature DB >> 21724259

Hirayama disease: an uncommon cause of distal upper extremity deficit.

C Darchis1, S Caron, A Lacour, M Toledano, T Boulanger, F Tempremant.   

Abstract

Hirayama disease is a myelopathy related to flexion movements of the neck that produce ischemic damage in the anterior horn of the cervical cord. The disease affects young people and is characterized by a distal upper extremity deficit that develops gradually. The diagnosis is confirmed by cervical magnetic resonance imaging (MRI) in flexion demonstrating a forward shift of the posterior dural sac and spinal cord compression. On radiology, there should be suggestive signs in neutral position such as cord atrophy, intramedullary bilateral high signal intensity on T2-weighted images, straightening of the cervical spine, and loss of attachment between the posterior dural sac and subjacent lamina. Exploration should be completed by an MR study in neck flexion. We report here on two typical cases of the disease and also include a review of the literature.
Copyright © 2011. Published by Elsevier Masson SAS.

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Year:  2011        PMID: 21724259     DOI: 10.1016/j.neurad.2011.05.001

Source DB:  PubMed          Journal:  J Neuroradiol        ISSN: 0150-9861            Impact factor:   3.447


  1 in total

Review 1.  [Hirayama disease: report of four Tunisian cases and review of literature].

Authors:  Sana Ben Amor; Anis Hassine; Ines Chatti; Anissa Khefifi; Mohamed Doggui; Mohamed Salah Harzallah; Sofien Benammou
Journal:  Pan Afr Med J       Date:  2015-04-16
  1 in total

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