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Infectious endocarditis complicated by an ischemic stroke and revealing Marfan syndrome
Marfan syndrome is a systematic genetic disease of the connective tissue. The cardiac affection would predict the prognosis and ischemic stroke might complicate it. The purpose of this work is to discuss the mechanisms of the ischemic stroke in Marfan syndrome which have to be considered in all youn...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications Pvt Ltd
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3144621/ https://www.ncbi.nlm.nih.gov/pubmed/21814418 http://dx.doi.org/10.4103/0975-3583.83041 |
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author | Souirti, Zouhayr Boujraf, Saïd Charai, Nadia Chtaou, Naïma Belahsen, Faouzi Messouak, Ouafae Messouak, Mohammed |
author_facet | Souirti, Zouhayr Boujraf, Saïd Charai, Nadia Chtaou, Naïma Belahsen, Faouzi Messouak, Ouafae Messouak, Mohammed |
author_sort | Souirti, Zouhayr |
collection | PubMed |
description | Marfan syndrome is a systematic genetic disease of the connective tissue. The cardiac affection would predict the prognosis and ischemic stroke might complicate it. The purpose of this work is to discuss the mechanisms of the ischemic stroke in Marfan syndrome which have to be considered in all young patients of ischemic strokes. We report the case of a 17-year-old male patient who presented with right hemiparesis with brachio-facial dominance, hemihypoesthesia and Broca's aphasia; these symptoms were followed by partial right somato-motor epileptic seizure. The cerebral computed tomographic (CT) scan demonstrated early signs of ischemic stroke in the left Sylvian artery. Cardiovascular examination revealed a systolic murmur in the mitral site. Marfan syndrome with infectious endocarditis complicated by ischemic stroke was diagnosed. However, the family pathological history was negative. The Marfan syndrome diagnosis was approved considering the following criteria: Ligamentous hyperlaxity, crystalline ectopia and mitral valve prolapsus with mitral insufficiency. The patient benefited of antibiotherapy for 4 weeks. The patient underwent sessions of motor physical therapy and orthophonic rehabilitation. Then, cardiac surgery was carried out and valvuloplasty was performed. The surgical treatment confirmed the presence of mitral insufficiency and prolapsus of the big mitral valve and multiple friable anterior-posterior vegetations with broken cordage of the small mitral valve. Replacement of the mitral valve was achieved, and the post-surgery follow-ups were simple. The diagnosis of Marfan syndrome was based on well-defined criteria. The evolution of the patient was marked by a complete improvement of the cardiac and motor deficits, and disappearance of the Broca's aphasia. A fibroelastic disease such Marfan syndrome has to be considered in unexplained ischemic stroke in all young patients. Hence, the diagnosis of Marfan syndrome involves an anticipation of the neurovascular complications by early cardiovascular care. |
format | Online Article Text |
id | pubmed-3144621 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-31446212011-08-03 Infectious endocarditis complicated by an ischemic stroke and revealing Marfan syndrome Souirti, Zouhayr Boujraf, Saïd Charai, Nadia Chtaou, Naïma Belahsen, Faouzi Messouak, Ouafae Messouak, Mohammed J Cardiovasc Dis Res Clinical Case Report Based Study Marfan syndrome is a systematic genetic disease of the connective tissue. The cardiac affection would predict the prognosis and ischemic stroke might complicate it. The purpose of this work is to discuss the mechanisms of the ischemic stroke in Marfan syndrome which have to be considered in all young patients of ischemic strokes. We report the case of a 17-year-old male patient who presented with right hemiparesis with brachio-facial dominance, hemihypoesthesia and Broca's aphasia; these symptoms were followed by partial right somato-motor epileptic seizure. The cerebral computed tomographic (CT) scan demonstrated early signs of ischemic stroke in the left Sylvian artery. Cardiovascular examination revealed a systolic murmur in the mitral site. Marfan syndrome with infectious endocarditis complicated by ischemic stroke was diagnosed. However, the family pathological history was negative. The Marfan syndrome diagnosis was approved considering the following criteria: Ligamentous hyperlaxity, crystalline ectopia and mitral valve prolapsus with mitral insufficiency. The patient benefited of antibiotherapy for 4 weeks. The patient underwent sessions of motor physical therapy and orthophonic rehabilitation. Then, cardiac surgery was carried out and valvuloplasty was performed. The surgical treatment confirmed the presence of mitral insufficiency and prolapsus of the big mitral valve and multiple friable anterior-posterior vegetations with broken cordage of the small mitral valve. Replacement of the mitral valve was achieved, and the post-surgery follow-ups were simple. The diagnosis of Marfan syndrome was based on well-defined criteria. The evolution of the patient was marked by a complete improvement of the cardiac and motor deficits, and disappearance of the Broca's aphasia. A fibroelastic disease such Marfan syndrome has to be considered in unexplained ischemic stroke in all young patients. Hence, the diagnosis of Marfan syndrome involves an anticipation of the neurovascular complications by early cardiovascular care. Medknow Publications Pvt Ltd 2011 /pmc/articles/PMC3144621/ /pubmed/21814418 http://dx.doi.org/10.4103/0975-3583.83041 Text en © Journal of Cardiovascular Disease Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Case Report Based Study Souirti, Zouhayr Boujraf, Saïd Charai, Nadia Chtaou, Naïma Belahsen, Faouzi Messouak, Ouafae Messouak, Mohammed Infectious endocarditis complicated by an ischemic stroke and revealing Marfan syndrome |
title | Infectious endocarditis complicated by an ischemic stroke and revealing Marfan syndrome |
title_full | Infectious endocarditis complicated by an ischemic stroke and revealing Marfan syndrome |
title_fullStr | Infectious endocarditis complicated by an ischemic stroke and revealing Marfan syndrome |
title_full_unstemmed | Infectious endocarditis complicated by an ischemic stroke and revealing Marfan syndrome |
title_short | Infectious endocarditis complicated by an ischemic stroke and revealing Marfan syndrome |
title_sort | infectious endocarditis complicated by an ischemic stroke and revealing marfan syndrome |
topic | Clinical Case Report Based Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3144621/ https://www.ncbi.nlm.nih.gov/pubmed/21814418 http://dx.doi.org/10.4103/0975-3583.83041 |
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