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Sporadic Creutzfeldt-Jakob Disease in 2 Plasma Product Recipients, United Kingdom
Sporadic Creutzfeldt-Jakob disease (sCJD) has not been previously reported in patients with clotting disorders treated with fractionated plasma products. We report 2 cases of sCJD identified in the United Kingdom in patients with a history of extended treatment for clotting disorders; 1 patient had...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Centers for Disease Control and Prevention
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443442/ https://www.ncbi.nlm.nih.gov/pubmed/28516863 http://dx.doi.org/10.3201/eid2306.161884 |
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author | Urwin, Patrick Thanigaikumar, Kumar Ironside, James W. Molesworth, Anna Knight, Richard S. Hewitt, Patricia E. Llewelyn, Charlotte Mackenzie, Jan Will, Robert G. |
author_facet | Urwin, Patrick Thanigaikumar, Kumar Ironside, James W. Molesworth, Anna Knight, Richard S. Hewitt, Patricia E. Llewelyn, Charlotte Mackenzie, Jan Will, Robert G. |
author_sort | Urwin, Patrick |
collection | PubMed |
description | Sporadic Creutzfeldt-Jakob disease (sCJD) has not been previously reported in patients with clotting disorders treated with fractionated plasma products. We report 2 cases of sCJD identified in the United Kingdom in patients with a history of extended treatment for clotting disorders; 1 patient had hemophilia B and the other von Willebrand disease. Both patients had been informed previously that they were at increased risk for variant CJD because of past treatment with fractionated plasma products sourced in the United Kingdom. However, both cases had clinical and investigative features suggestive of sCJD. This diagnosis was confirmed in both cases on neuropathologic and biochemical analysis of the brain. A causal link between the treatment with plasma products and the development of sCJD has not been established, and the occurrence of these cases may simply reflect a chance event in the context of systematic surveillance for CJD in large populations. |
format | Online Article Text |
id | pubmed-5443442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Centers for Disease Control and Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-54434422017-06-02 Sporadic Creutzfeldt-Jakob Disease in 2 Plasma Product Recipients, United Kingdom Urwin, Patrick Thanigaikumar, Kumar Ironside, James W. Molesworth, Anna Knight, Richard S. Hewitt, Patricia E. Llewelyn, Charlotte Mackenzie, Jan Will, Robert G. Emerg Infect Dis Synopsis Sporadic Creutzfeldt-Jakob disease (sCJD) has not been previously reported in patients with clotting disorders treated with fractionated plasma products. We report 2 cases of sCJD identified in the United Kingdom in patients with a history of extended treatment for clotting disorders; 1 patient had hemophilia B and the other von Willebrand disease. Both patients had been informed previously that they were at increased risk for variant CJD because of past treatment with fractionated plasma products sourced in the United Kingdom. However, both cases had clinical and investigative features suggestive of sCJD. This diagnosis was confirmed in both cases on neuropathologic and biochemical analysis of the brain. A causal link between the treatment with plasma products and the development of sCJD has not been established, and the occurrence of these cases may simply reflect a chance event in the context of systematic surveillance for CJD in large populations. Centers for Disease Control and Prevention 2017-06 /pmc/articles/PMC5443442/ /pubmed/28516863 http://dx.doi.org/10.3201/eid2306.161884 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited. |
spellingShingle | Synopsis Urwin, Patrick Thanigaikumar, Kumar Ironside, James W. Molesworth, Anna Knight, Richard S. Hewitt, Patricia E. Llewelyn, Charlotte Mackenzie, Jan Will, Robert G. Sporadic Creutzfeldt-Jakob Disease in 2 Plasma Product Recipients, United Kingdom |
title | Sporadic Creutzfeldt-Jakob Disease in 2 Plasma Product Recipients, United Kingdom |
title_full | Sporadic Creutzfeldt-Jakob Disease in 2 Plasma Product Recipients, United Kingdom |
title_fullStr | Sporadic Creutzfeldt-Jakob Disease in 2 Plasma Product Recipients, United Kingdom |
title_full_unstemmed | Sporadic Creutzfeldt-Jakob Disease in 2 Plasma Product Recipients, United Kingdom |
title_short | Sporadic Creutzfeldt-Jakob Disease in 2 Plasma Product Recipients, United Kingdom |
title_sort | sporadic creutzfeldt-jakob disease in 2 plasma product recipients, united kingdom |
topic | Synopsis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443442/ https://www.ncbi.nlm.nih.gov/pubmed/28516863 http://dx.doi.org/10.3201/eid2306.161884 |
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