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...

Descripción completa

Detalles Bibliográficos
Autores principales: Chibli, Radia, Omor, Youssef, Sebbouba, Nadir Slimani, Hassani, Moulay Rachid El, Jiddane, Mohamed, Fikri, Meriem
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
Descripción
Sumario: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.