Cargando…
Moya moya: étiologie rare d’accident vasculaire cérébral ischémique chez l’enfant: à propos d’un cas
Moya moya disease is an angiogenic disease characterized by the narrowing of the distal internal carotid artery extending to the proximal segments of the middle and anterior cerebral arteries, inducing collateral vessels formation. These vessels come from the collateral parenchymal vessels, the perf...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5871250/ https://www.ncbi.nlm.nih.gov/pubmed/29599890 http://dx.doi.org/10.11604/pamj.2017.28.192.8740 |
_version_ | 1783309609400795136 |
---|---|
author | Chibli, Radia Omor, Youssef Sebbouba, Nadir Slimani Hassani, Moulay Rachid El Jiddane, Mohamed Fikri, Meriem |
author_facet | Chibli, Radia Omor, Youssef Sebbouba, Nadir Slimani Hassani, Moulay Rachid El Jiddane, Mohamed Fikri, Meriem |
author_sort | Chibli, Radia |
collection | PubMed |
description | Moya moya disease is an angiogenic disease characterized by the narrowing of the distal internal carotid artery extending to the proximal segments of the middle and anterior cerebral arteries, inducing collateral vessels formation. These vessels come from the collateral parenchymal vessels, the perforating vessels, leptomeningeal vessels and other transdural anastomoses. These collateral vessels have a characteristic appearance on angiography, forming a cloud of smoke: net-like moyamoya. Its etiology is still poorly understood. Moyamoya disease accounts for 10-15% of the causes of stroke, with 2 age peaks at which its occurrence is more frequent: children around 5 years old and adults around 40 years old. Its evolution can be slow with intermittent symptoms or fulminant with fast neurological deterioration. The current data show the role of surgery as the gold standard for the treatment of moyamoya syndrome, in particular in patients with progressive and recurrent symptoms. |
format | Online Article Text |
id | pubmed-5871250 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The African Field Epidemiology Network |
record_format | MEDLINE/PubMed |
spelling | pubmed-58712502018-03-29 Moya moya: étiologie rare d’accident vasculaire cérébral ischémique chez l’enfant: à propos d’un cas Chibli, Radia Omor, Youssef Sebbouba, Nadir Slimani Hassani, Moulay Rachid El Jiddane, Mohamed Fikri, Meriem Pan Afr Med J Case Report Moya moya disease is an angiogenic disease characterized by the narrowing of the distal internal carotid artery extending to the proximal segments of the middle and anterior cerebral arteries, inducing collateral vessels formation. These vessels come from the collateral parenchymal vessels, the perforating vessels, leptomeningeal vessels and other transdural anastomoses. These collateral vessels have a characteristic appearance on angiography, forming a cloud of smoke: net-like moyamoya. Its etiology is still poorly understood. Moyamoya disease accounts for 10-15% of the causes of stroke, with 2 age peaks at which its occurrence is more frequent: children around 5 years old and adults around 40 years old. Its evolution can be slow with intermittent symptoms or fulminant with fast neurological deterioration. The current data show the role of surgery as the gold standard for the treatment of moyamoya syndrome, in particular in patients with progressive and recurrent symptoms. The African Field Epidemiology Network 2017-11-01 /pmc/articles/PMC5871250/ /pubmed/29599890 http://dx.doi.org/10.11604/pamj.2017.28.192.8740 Text en © Radia Chibli et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Chibli, Radia Omor, Youssef Sebbouba, Nadir Slimani Hassani, Moulay Rachid El Jiddane, Mohamed Fikri, Meriem Moya moya: étiologie rare d’accident vasculaire cérébral ischémique chez l’enfant: à propos d’un cas |
title | Moya moya: étiologie rare d’accident vasculaire cérébral ischémique chez l’enfant: à propos d’un cas |
title_full | Moya moya: étiologie rare d’accident vasculaire cérébral ischémique chez l’enfant: à propos d’un cas |
title_fullStr | Moya moya: étiologie rare d’accident vasculaire cérébral ischémique chez l’enfant: à propos d’un cas |
title_full_unstemmed | Moya moya: étiologie rare d’accident vasculaire cérébral ischémique chez l’enfant: à propos d’un cas |
title_short | Moya moya: étiologie rare d’accident vasculaire cérébral ischémique chez l’enfant: à propos d’un cas |
title_sort | moya moya: étiologie rare d’accident vasculaire cérébral ischémique chez l’enfant: à propos d’un cas |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5871250/ https://www.ncbi.nlm.nih.gov/pubmed/29599890 http://dx.doi.org/10.11604/pamj.2017.28.192.8740 |
work_keys_str_mv | AT chibliradia moyamoyaetiologieraredaccidentvasculairecerebralischemiquechezlenfantaproposduncas AT omoryoussef moyamoyaetiologieraredaccidentvasculairecerebralischemiquechezlenfantaproposduncas AT sebboubanadirslimani moyamoyaetiologieraredaccidentvasculairecerebralischemiquechezlenfantaproposduncas AT hassanimoulayrachidel moyamoyaetiologieraredaccidentvasculairecerebralischemiquechezlenfantaproposduncas AT jiddanemohamed moyamoyaetiologieraredaccidentvasculairecerebralischemiquechezlenfantaproposduncas AT fikrimeriem moyamoyaetiologieraredaccidentvasculairecerebralischemiquechezlenfantaproposduncas |