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Cyclophosphamide-induced posterior reversible encephalopathy syndrome (PRES): a case report
INTRODUCTION: Posterior reversible encephalopathy syndrome is a clinicoradiologic entity characterized by headache, seizures, decreased vision, impaired consciousness and white matter oedema in bilateral occipitoparietal regions. Hypertensive encephalopathy, eclampsia, immunosuppressive/cytotoxic dr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4301836/ https://www.ncbi.nlm.nih.gov/pubmed/25519913 http://dx.doi.org/10.1186/1752-1947-8-442 |
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author | Jayaweera, Jayamalee L Withana, Milinda R Dalpatadu, Chamila KP Beligaswatta, Chathurika D Rajapakse, Thamara Jayasinghe, Saroj Chang, Thashi |
author_facet | Jayaweera, Jayamalee L Withana, Milinda R Dalpatadu, Chamila KP Beligaswatta, Chathurika D Rajapakse, Thamara Jayasinghe, Saroj Chang, Thashi |
author_sort | Jayaweera, Jayamalee L |
collection | PubMed |
description | INTRODUCTION: Posterior reversible encephalopathy syndrome is a clinicoradiologic entity characterized by headache, seizures, decreased vision, impaired consciousness and white matter oedema in bilateral occipitoparietal regions. Hypertensive encephalopathy, eclampsia, immunosuppressive/cytotoxic drugs, organ transplantation, renal disease, autoimmune diseases and vasculitides are reported risk factors of posterior reversible encephalopathy syndrome. Reports of cyclophosphamide-induced posterior reversible encephalopathy syndrome are rare and occurred in a background of renal failure, fluid overload or active connective tissue disease. CASE PRESENTATION: We report a case of posterior reversible encephalopathy syndrome developing as a direct consequence of intravenous cyclophosphamide therapy in a 33-year-old normotensive Sri Lankan woman with lupus nephritis but quiescent disease activity and normal renal function. CONCLUSIONS: This case report highlights the need for awareness and early recognition of this rare but serious adverse effect of cyclophosphamide that occurred in the absence of other known risk factors of posterior reversible encephalopathy syndrome and that early appropriate intervention leads to a good outcome. |
format | Online Article Text |
id | pubmed-4301836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43018362015-01-22 Cyclophosphamide-induced posterior reversible encephalopathy syndrome (PRES): a case report Jayaweera, Jayamalee L Withana, Milinda R Dalpatadu, Chamila KP Beligaswatta, Chathurika D Rajapakse, Thamara Jayasinghe, Saroj Chang, Thashi J Med Case Rep Case Report INTRODUCTION: Posterior reversible encephalopathy syndrome is a clinicoradiologic entity characterized by headache, seizures, decreased vision, impaired consciousness and white matter oedema in bilateral occipitoparietal regions. Hypertensive encephalopathy, eclampsia, immunosuppressive/cytotoxic drugs, organ transplantation, renal disease, autoimmune diseases and vasculitides are reported risk factors of posterior reversible encephalopathy syndrome. Reports of cyclophosphamide-induced posterior reversible encephalopathy syndrome are rare and occurred in a background of renal failure, fluid overload or active connective tissue disease. CASE PRESENTATION: We report a case of posterior reversible encephalopathy syndrome developing as a direct consequence of intravenous cyclophosphamide therapy in a 33-year-old normotensive Sri Lankan woman with lupus nephritis but quiescent disease activity and normal renal function. CONCLUSIONS: This case report highlights the need for awareness and early recognition of this rare but serious adverse effect of cyclophosphamide that occurred in the absence of other known risk factors of posterior reversible encephalopathy syndrome and that early appropriate intervention leads to a good outcome. BioMed Central 2014-12-18 /pmc/articles/PMC4301836/ /pubmed/25519913 http://dx.doi.org/10.1186/1752-1947-8-442 Text en © Jayaweera et al.; licensee BioMed Central. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Jayaweera, Jayamalee L Withana, Milinda R Dalpatadu, Chamila KP Beligaswatta, Chathurika D Rajapakse, Thamara Jayasinghe, Saroj Chang, Thashi Cyclophosphamide-induced posterior reversible encephalopathy syndrome (PRES): a case report |
title | Cyclophosphamide-induced posterior reversible encephalopathy syndrome (PRES): a case report |
title_full | Cyclophosphamide-induced posterior reversible encephalopathy syndrome (PRES): a case report |
title_fullStr | Cyclophosphamide-induced posterior reversible encephalopathy syndrome (PRES): a case report |
title_full_unstemmed | Cyclophosphamide-induced posterior reversible encephalopathy syndrome (PRES): a case report |
title_short | Cyclophosphamide-induced posterior reversible encephalopathy syndrome (PRES): a case report |
title_sort | cyclophosphamide-induced posterior reversible encephalopathy syndrome (pres): a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4301836/ https://www.ncbi.nlm.nih.gov/pubmed/25519913 http://dx.doi.org/10.1186/1752-1947-8-442 |
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