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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Main Authors: Isabella Canavero, Ignazio Gaspare Vetrano, Marialuisa Zedde, Rosario Pascarella, Laura Gatti, Francesco Acerbi, Sara Nava, Paolo Ferroli, Eugenio Agostino Parati, Anna Bersano
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:Journal of Clinical Medicine
Subjects:
Online Access:https://www.mdpi.com/2077-0383/10/16/3628
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spelling 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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