Clinical Management of Moyamoya Patients
Moyamoya angiopathy (MMA) is a peculiar cerebrovascular condition characterized by progressive steno-occlusion of the terminal part of the internal carotid arteries (ICAs) and their proximal branches, associated with the development of a network of fragile collateral vessels at the base of the brain...
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doaj-83ca9b84d7e44584b383a103dfc3397b2021-08-26T13:55:36ZengMDPI AGJournal of Clinical Medicine2077-03832021-08-01103628362810.3390/jcm10163628Clinical Management of Moyamoya PatientsIsabella Canavero0Ignazio Gaspare Vetrano1Marialuisa Zedde2Rosario Pascarella3Laura Gatti4Francesco Acerbi5Sara Nava6Paolo Ferroli7Eugenio Agostino Parati8Anna Bersano9Cerebrovascular Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, ItalyDepartment of Neurosurgery, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, ItalyNeurology Unit-Stroke Unit, Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, 42122 Reggio Emilia, ItalyNeuroradiology Unit, Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, 42122 Reggio Emilia, ItalyCellular Neurobiology Laboratory, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, ItalyDepartment of Neurosurgery, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, ItalyCell Therapy Production Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, ItalyDepartment of Neurosurgery, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, ItalyNeurorehabilitation Department, IRCCS Istituti Clinici Scientifici Maugeri, 20138 Milan, ItalyCerebrovascular Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, ItalyMoyamoya angiopathy (MMA) is a peculiar cerebrovascular condition characterized by progressive steno-occlusion of the terminal part of the internal carotid arteries (ICAs) and their proximal branches, associated with the development of a network of fragile collateral vessels at the base of the brain. The diagnosis is essentially made by radiological angiographic techniques. MMA is often idiopathic (moyamoya disease-MMD); conversely, it can be associated with acquired or hereditary conditions (moyamoya Syndrome-MMS); however, the pathophysiology underlying either MMD or MMS has not been fully elucidated to date, and this poor knowledge reflects uncertainties and heterogeneity in patient management. MMD and MMS also have similar clinical expressions, including, above all, ischemic and hemorrhagic strokes, then headaches, seizures, cognitive impairment, and movement disorders. The available treatment strategies are currently shared between idiopathic MMD and MMS, including pharmacological and surgical stroke prevention treatments and symptomatic drugs. No pharmacological treatment able to reverse the progressive disappearance of the ICAs has been found to date in both idiopathic and syndromic cases. Antithrombotic agents are usually prescribed in ischemic MMA, although the coexisting hemorrhagic risk should be considered. Surgical revascularization techniques, which are currently the best available treatment in symptomatic MMA, are associated with good long-term outcomes and reduced ischemic and hemorrhagic risks. Given the lack of dedicated randomized clinical trials, current treatment is mainly based on observational studies and physicians’ and surgeons’ expertise.https://www.mdpi.com/2077-0383/10/16/3628moyamoya angiopathymoyamoya diseasemoyamoya syndromediagnosismanagementtherapy |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Isabella Canavero Ignazio Gaspare Vetrano Marialuisa Zedde Rosario Pascarella Laura Gatti Francesco Acerbi Sara Nava Paolo Ferroli Eugenio Agostino Parati Anna Bersano |
spellingShingle |
Isabella Canavero Ignazio Gaspare Vetrano Marialuisa Zedde Rosario Pascarella Laura Gatti Francesco Acerbi Sara Nava Paolo Ferroli Eugenio Agostino Parati Anna Bersano Clinical Management of Moyamoya Patients Journal of Clinical Medicine moyamoya angiopathy moyamoya disease moyamoya syndrome diagnosis management therapy |
author_facet |
Isabella Canavero Ignazio Gaspare Vetrano Marialuisa Zedde Rosario Pascarella Laura Gatti Francesco Acerbi Sara Nava Paolo Ferroli Eugenio Agostino Parati Anna Bersano |
author_sort |
Isabella Canavero |
title |
Clinical Management of Moyamoya Patients |
title_short |
Clinical Management of Moyamoya Patients |
title_full |
Clinical Management of Moyamoya Patients |
title_fullStr |
Clinical Management of Moyamoya Patients |
title_full_unstemmed |
Clinical Management of Moyamoya Patients |
title_sort |
clinical management of moyamoya patients |
publisher |
MDPI AG |
series |
Journal of Clinical Medicine |
issn |
2077-0383 |
publishDate |
2021-08-01 |
description |
Moyamoya angiopathy (MMA) is a peculiar cerebrovascular condition characterized by progressive steno-occlusion of the terminal part of the internal carotid arteries (ICAs) and their proximal branches, associated with the development of a network of fragile collateral vessels at the base of the brain. The diagnosis is essentially made by radiological angiographic techniques. MMA is often idiopathic (moyamoya disease-MMD); conversely, it can be associated with acquired or hereditary conditions (moyamoya Syndrome-MMS); however, the pathophysiology underlying either MMD or MMS has not been fully elucidated to date, and this poor knowledge reflects uncertainties and heterogeneity in patient management. MMD and MMS also have similar clinical expressions, including, above all, ischemic and hemorrhagic strokes, then headaches, seizures, cognitive impairment, and movement disorders. The available treatment strategies are currently shared between idiopathic MMD and MMS, including pharmacological and surgical stroke prevention treatments and symptomatic drugs. No pharmacological treatment able to reverse the progressive disappearance of the ICAs has been found to date in both idiopathic and syndromic cases. Antithrombotic agents are usually prescribed in ischemic MMA, although the coexisting hemorrhagic risk should be considered. Surgical revascularization techniques, which are currently the best available treatment in symptomatic MMA, are associated with good long-term outcomes and reduced ischemic and hemorrhagic risks. Given the lack of dedicated randomized clinical trials, current treatment is mainly based on observational studies and physicians’ and surgeons’ expertise. |
topic |
moyamoya angiopathy moyamoya disease moyamoya syndrome diagnosis management therapy |
url |
https://www.mdpi.com/2077-0383/10/16/3628 |
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