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Stroke in hereditary hemorrhagic telangiectasia patients. New evidence for repeated screening and early treatment of pulmonary vascular malformations: two case reports
BACKGROUND: Paradoxical embolism due to pulmonary arteriovenous malformations is the main mechanism of brain infarction in patients with hereditary hemorrhagic telangiectasia. International Guidelines have recently been published to clarify the performance of screening tests and the effectiveness of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3148967/ https://www.ncbi.nlm.nih.gov/pubmed/21740592 http://dx.doi.org/10.1186/1471-2377-11-84 |
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author | Ribeiro, Espartaco Cogez, Julien Babin, Emmanuel Viader, Fausto Defer, Gilles |
author_facet | Ribeiro, Espartaco Cogez, Julien Babin, Emmanuel Viader, Fausto Defer, Gilles |
author_sort | Ribeiro, Espartaco |
collection | PubMed |
description | BACKGROUND: Paradoxical embolism due to pulmonary arteriovenous malformations is the main mechanism of brain infarction in patients with hereditary hemorrhagic telangiectasia. International Guidelines have recently been published to clarify the performance of screening tests and the effectiveness of treatment for pulmonary arteriovenous malformations. CASE PRESENTATION: We present two cases of hereditary hemorrhagic telangiectasia patients of our hospital who experienced an acute stroke secondary to paradoxical embolism. CONCLUSIONS: These two cases show that the guidelines must be followed to prevent the occurrence of ischemic stroke in patients with hereditary hemorrhagic telangiectasia, and that although they may be adequate in most cases, there are some patients who need a more personalized approach. |
format | Online Article Text |
id | pubmed-3148967 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31489672011-08-03 Stroke in hereditary hemorrhagic telangiectasia patients. New evidence for repeated screening and early treatment of pulmonary vascular malformations: two case reports Ribeiro, Espartaco Cogez, Julien Babin, Emmanuel Viader, Fausto Defer, Gilles BMC Neurol Case Report BACKGROUND: Paradoxical embolism due to pulmonary arteriovenous malformations is the main mechanism of brain infarction in patients with hereditary hemorrhagic telangiectasia. International Guidelines have recently been published to clarify the performance of screening tests and the effectiveness of treatment for pulmonary arteriovenous malformations. CASE PRESENTATION: We present two cases of hereditary hemorrhagic telangiectasia patients of our hospital who experienced an acute stroke secondary to paradoxical embolism. CONCLUSIONS: These two cases show that the guidelines must be followed to prevent the occurrence of ischemic stroke in patients with hereditary hemorrhagic telangiectasia, and that although they may be adequate in most cases, there are some patients who need a more personalized approach. BioMed Central 2011-07-09 /pmc/articles/PMC3148967/ /pubmed/21740592 http://dx.doi.org/10.1186/1471-2377-11-84 Text en Copyright ©2011 Ribeiro et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Ribeiro, Espartaco Cogez, Julien Babin, Emmanuel Viader, Fausto Defer, Gilles Stroke in hereditary hemorrhagic telangiectasia patients. New evidence for repeated screening and early treatment of pulmonary vascular malformations: two case reports |
title | Stroke in hereditary hemorrhagic telangiectasia patients. New evidence for repeated screening and early treatment of pulmonary vascular malformations: two case reports |
title_full | Stroke in hereditary hemorrhagic telangiectasia patients. New evidence for repeated screening and early treatment of pulmonary vascular malformations: two case reports |
title_fullStr | Stroke in hereditary hemorrhagic telangiectasia patients. New evidence for repeated screening and early treatment of pulmonary vascular malformations: two case reports |
title_full_unstemmed | Stroke in hereditary hemorrhagic telangiectasia patients. New evidence for repeated screening and early treatment of pulmonary vascular malformations: two case reports |
title_short | Stroke in hereditary hemorrhagic telangiectasia patients. New evidence for repeated screening and early treatment of pulmonary vascular malformations: two case reports |
title_sort | stroke in hereditary hemorrhagic telangiectasia patients. new evidence for repeated screening and early treatment of pulmonary vascular malformations: two case reports |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3148967/ https://www.ncbi.nlm.nih.gov/pubmed/21740592 http://dx.doi.org/10.1186/1471-2377-11-84 |
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