Raciborska, DD;
Noyce, AJ;
Pyne, D;
Turner, BP;
(2018)
Lupus myelopathy.
Practical Neurology
, 18
(1)
pp. 66-69.
10.1136/practneurol-2017-001756.
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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.
Type: | Article |
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Title: | Lupus myelopathy |
Location: | England |
Open access status: | An open access version is available from UCL Discovery |
DOI: | 10.1136/practneurol-2017-001756 |
Publisher version: | http://doi.org/10.1136/practneurol-2017-001756 |
Language: | English |
Additional information: | This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions. |
Keywords: | Central nervous system (CNS), Myelopathy, Neurological disorders, Lupus-related myelopathy, CNS infections, Cyclophosphamide, Methylprednisolone |
UCL classification: | UCL UCL > Provost and Vice Provost Offices UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology |
URI: | https://discovery.ucl.ac.uk/id/eprint/10042849 |
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