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Acute Respiratory Distress Syndrome and Posterior Reversible Encephalopathy Syndrome following Rituximab Therapy

The anti-CD20 monoclonal antibody rituximab is associated with rare but significant adverse events, notably posterior reversible encephalopathy syndrome (PRES) and acute respiratory distress syndrome (ARDS). We report a case of concomitant ARDS and PRES developing after rituximab therapy for treatme...

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Detalles Bibliográficos
Autores principales: Wardrope, Katrina E., Manson, Lynn, Metcalfe, Wendy, Sullivan, Eoin D. O
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4886031/
https://www.ncbi.nlm.nih.gov/pubmed/27275457
http://dx.doi.org/10.1159/000444250
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author Wardrope, Katrina E.
Manson, Lynn
Metcalfe, Wendy
Sullivan, Eoin D. O
author_facet Wardrope, Katrina E.
Manson, Lynn
Metcalfe, Wendy
Sullivan, Eoin D. O
author_sort Wardrope, Katrina E.
collection PubMed
description The anti-CD20 monoclonal antibody rituximab is associated with rare but significant adverse events, notably posterior reversible encephalopathy syndrome (PRES) and acute respiratory distress syndrome (ARDS). We report a case of concomitant ARDS and PRES developing after rituximab therapy for treatment of cryoglobulinaemic vasculitis. There are 7 reported cases of PRES complicating rituximab use. PRES onset varied from immediate to 21 days after administration. All patients recovered completely, and rituximab was reintroduced in half of the cases. The occurrence of ARDS in association with rituximab is rarer. Only 3 confirmed cases exist, and ARDS may occur as a delayed reaction.
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spelling pubmed-48860312016-06-06 Acute Respiratory Distress Syndrome and Posterior Reversible Encephalopathy Syndrome following Rituximab Therapy Wardrope, Katrina E. Manson, Lynn Metcalfe, Wendy Sullivan, Eoin D. O Case Rep Nephrol Dial Published online: February, 2016 The anti-CD20 monoclonal antibody rituximab is associated with rare but significant adverse events, notably posterior reversible encephalopathy syndrome (PRES) and acute respiratory distress syndrome (ARDS). We report a case of concomitant ARDS and PRES developing after rituximab therapy for treatment of cryoglobulinaemic vasculitis. There are 7 reported cases of PRES complicating rituximab use. PRES onset varied from immediate to 21 days after administration. All patients recovered completely, and rituximab was reintroduced in half of the cases. The occurrence of ARDS in association with rituximab is rarer. Only 3 confirmed cases exist, and ARDS may occur as a delayed reaction. S. Karger AG 2016-02-24 /pmc/articles/PMC4886031/ /pubmed/27275457 http://dx.doi.org/10.1159/000444250 Text en Copyright © 2016 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Published online: February, 2016
Wardrope, Katrina E.
Manson, Lynn
Metcalfe, Wendy
Sullivan, Eoin D. O
Acute Respiratory Distress Syndrome and Posterior Reversible Encephalopathy Syndrome following Rituximab Therapy
title Acute Respiratory Distress Syndrome and Posterior Reversible Encephalopathy Syndrome following Rituximab Therapy
title_full Acute Respiratory Distress Syndrome and Posterior Reversible Encephalopathy Syndrome following Rituximab Therapy
title_fullStr Acute Respiratory Distress Syndrome and Posterior Reversible Encephalopathy Syndrome following Rituximab Therapy
title_full_unstemmed Acute Respiratory Distress Syndrome and Posterior Reversible Encephalopathy Syndrome following Rituximab Therapy
title_short Acute Respiratory Distress Syndrome and Posterior Reversible Encephalopathy Syndrome following Rituximab Therapy
title_sort acute respiratory distress syndrome and posterior reversible encephalopathy syndrome following rituximab therapy
topic Published online: February, 2016
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4886031/
https://www.ncbi.nlm.nih.gov/pubmed/27275457
http://dx.doi.org/10.1159/000444250
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