A case of posterior reversible encephalopathy syndrome after plasma exchange for severe IgA vasculitis
Author:
Affiliation:
1. Tomishiro Central Hospital Department of Kidney, Rheumatology, Collaborative Disease
2. Tomishiro Central Hospital Department of Clinical Research Center
Publisher
Japanese Society for Dialysis Therapy
Subject
Organic Chemistry,Biochemistry
Link
https://www.jstage.jst.go.jp/article/jsdt/52/8/52_491/_pdf
Reference6 articles.
1. 2) Ozen S, Pistorio A, Iusan SM, et al. EULAR/PRINTO/PRES criteria for Henoch-Schönlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part Ⅱ: Final classification criteria. Ann Rheum Dis 2010; 69: 798-806.
2. 3) Garzoni L, Vanoni F, Rizzi M, et al. Nervous system dysfunction in Henoch−Schönlein syndrome: systematic review of the literature. Rheumatology (Oxford) 2009; 48: 1524-9.
3. 4) Pillebout E, Thervet E, Hill G, Albert C, Vanhille P, Nochy D. Henoch-Schönlein purpura in adults: outcome and prognostic factors. J Am Soc Nephrol 2002; 13: 1271-8.
4. 5) Stefek B, Beck M, Ioffreda M, Gardner L, Stefanski M. Henoch-Schönlein Purpura with Posterior Reversible Encephalopathy Syndrome. J Pediatr 2015; 167: 1152-4.
5. 6) Fugate JE, Rabinstein AA. Posterior reversible encephalopathy syndrome: clinical and radiological manifestations, pathophysiology, and outstanding questions. Lancet Neurol 2015; 14: 914-925.
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