Key result
Review highlights recent advances in clinical characteristics, imaging, and surgical management of moyamoya disease.
Moyamoya is a rare disorder that involves steno-occlusive arterial changes of the anterior circulation, along with proliferative development of basal arterial collaterals. It is either idiopathic (called moyamoya disease) or the result of a specific underlying condition such as atherosclerosis, radiation therapy, or sickle cell disease (called moyamoya syndrome or phenomenon). In recent years, numerous insights into and advances in the understanding, evaluation, and management of moyamoya patients have occurred. This article briefly reviews the spectrum of moyamoya conditions and then provides a synopsis of numerous recent investigations that shed light on various aspects of the disease, including its clinical characteristics, natural history, underlying pathology, imaging, surgical techniques, and long-term patient outcome. ABBREVIATIONS: CBF, cerebral blood flow EDAS, encephaloduroarteriosynangiosis MCA, middle cerebral artery MMD, moyamoya disease STA, superficial temporal artery TIA, transient ischemic attack
No takes yet. Share an insight, caveat, or question.
Arias et al. (2014) conducted a review in Moyamoya disease. Surgical techniques and management was evaluated. This article reviews recent advances in the clinical characteristics, natural history, pathology, imaging, surgical techniques, and management of moyamoya disease.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: