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Case Report
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| Recurrent posterior reversible encephalopathy syndrome in systemic lupus erythematosus | ||||||
| Melissa Ng1, Sadia Saber1, Richard Stratton1 | ||||||
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1Royal Free Hospital, Pond Street, London, United Kingdom
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| How to cite this article |
| Ng M, Saber S, Stratton R. Recurrent posterior reversible encephalopathy syndrome in systemic lupus erythematosus. Int J Case Rep Images 2017;8(11):725–728. |
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ABSTRACT
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Posterior reversible encephalopathy syndrome (PRES) is an acute encephalopathy that manifests as headache, visual disturbance, altered mental state, and seizures. There are striking characteristic findings on neuroimaging. The PRES is associated with a number of conditions, including autoimmune disease. We describe the case of a 37-year-old female with a history of systemic lupus erythematosus presenting with headache and visual changes. Prompt diagnosis in PRES is important because if it is not recognized and treated early, it may progress to irreversible neurological damage. This patient made a good initial recovery, but suffered a relapse secondary to severe resistant lupus nephritis and refractory hypertension. Keywords: Encephalopathy, Headache, Lupus, Posterior reversible encephalopathy syndrome (PRES), Systemic lupus erythematosus (SLE) |
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Author Contributions
Melissa Ng – Substantial contributions to conception and design, Acquisition of data, Analysis and interpretation of data, Drafting the article, Revising it critically for important intellectual content, Final approval of the version to be published Sadia Saber – Substantial contributions to conception and design, Acquisition of data, Revising it critically for important intellectual content, Final approval of the version to be published Richard Stratton – Substantial contributions to conception and design, Acquisition of data, Analysis and interpretation of data, Revising it critically for important intellectual content, Final approval of the version to be published |
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Guarantor
The corresponding author is the guarantor of submission. |
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Source of support
None |
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Conflict of interest
Authors declare no conflict of interest. |
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Copyright
© 2017 Melissa Ng et al. This article is distributed under the terms of Creative Commons Attribution License which permits unrestricted use, distribution and reproduction in any medium provided the original author(s) and original publisher are properly credited. Please see the copyright policy on the journal website for more information. |
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