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Lupus myelopathy
  1. Dominika D Raciborska1,
  2. Alastair John Noyce2,3,
  3. Dev Pyne4,
  4. Benjamin P Turner3
  1. 1Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK
  2. 2Preventive Neurology Unit, Wolfson Institute of Preventive Medicine, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK
  3. 3Department of Neurology, Royal London Hospital, London, UK
  4. 4Department of Rheumatology, Royal London Hospital, London, UK
  1. Correspondence to Dominika D Raciborska, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London E1 1BB, UK; nika.raciborska{at}gmail.com

Abstract

Although neurological manifestations of systemic lupus erythematosus (SLE) are well recognised, myelopathy complicating SLE is rare. A 35-year-old woman presented with non-specific symptoms and a respiratory tract infection but had serological evidence of SLE. She subsequently deteriorated rapidly, developing a catastrophic spinal cord syndrome. Her initial MRI was normal; but after 1 month, her encephalopathy having progressed, repeat imaging showed characteristic myelitic changes. She responded only slowly to a combination of cyclophosphamide and corticosteroids. This case exemplifies the mixed presentations of SLE, including the under-recognised ‘subpial leukomyelopathy’ of central nervous system lupus. It highlights the challenges in managing lupus-related myelopathy and the benefits of a multidisciplinary approach to care.

  • sle
  • myelopathy
  • neuroimmunology
  • rheumatology
  • neuropharmacology

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Footnotes

  • Contributors DR did literature review and provided the first drafts of the case. AN, DP and BT were involved in management of the patient as well as writing and reviewing the case.

  • Competing interests None declared.

  • Patient consent Obtained.

  • Provenance and peer review Not commissioned; externally peer reviewed. This paper was reviewed by Fady Joseph, South Wales, UK.

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