PRECISION REVASCULARIZATION IN ADULT MOYAMOYA DISEASE: HEMODYNAMIC PHENOTYPING, DIRECT AND COMBINED BYPASS, HYPERPERFUSION CONTROL, AND PERSONALIZED SURGICAL TARGETING Abstract
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Background. Adult moyamoya disease is a progressive occlusive cerebrovascular arteriopathy characterized by stenosis of the terminal internal carotid circulation, development of fragile collateral networks, impaired cerebrovascular reserve, and risk of ischemic or hemorrhagic stroke. Surgical revascularization is the principal disease-modifying treatment in symptomatic and hemodynamically compromised patients. However, the optimal strategy cannot be reduced to a universal choice between direct, indirect, and combined bypass because adult moyamoya disease encompasses heterogeneous ischemic, hemorrhagic, asymptomatic, cognitive, and collateral-dominant phenotypes.
Materials and Methods. A structured narrative review was performed using contemporary guidelines, randomized and prospective studies, population-based cohorts, hemodynamic investigations, and surgical series published through August 2026. Evidence was synthesized regarding direct superficial temporal artery–middle cerebral artery bypass, indirect synangiosis, combined revascularization, cerebral perfusion imaging, cerebrovascular reserve, periventricular collateral anatomy, postoperative hyperperfusion, cerebral infarction, cognition, and genetic predictors of revascularization.
Results. Direct bypass provides immediate flow augmentation, whereas indirect procedures depend on delayed extracranial–intracranial neoangiogenesis. Combined surgery offers both mechanisms and may provide broader long-term revascularization in adults. Hemorrhagic moyamoya represents a distinct surgical phenotype in which bypass can reduce rebleeding risk, particularly in patients with high-risk posterior hemorrhage and fragile periventricular collateral pathways. In ischemic moyamoya, surgical selection should integrate symptoms with objective hemodynamic compromise rather than angiographic stenosis alone. Cerebral hyperperfusion syndrome remains a major postoperative complication after direct bypass and is associated with impaired autoregulation, regional perfusion abnormalities, and abrupt redistribution of blood flow. Newer CT perfusion, arterial spin labeling, Flow800, Doppler, and genetic approaches are increasingly capable of predicting postoperative perfusion patterns and neoangiogenesis.
Conclusion. Adult moyamoya surgery is evolving from standardized bypass selection toward precision revascularization. The optimal operation should be determined by clinical phenotype, regional cerebrovascular reserve, collateral architecture, recipient-vessel anatomy, genetic background, and predicted perioperative hemodynamic response. Direct flow augmentation and indirect neoangiogenesis should be regarded as complementary physiological tools rather than competing techniques.
Keywords: moyamoya disease; cerebral revascularization; STA–MCA bypass; combined bypass; indirect bypass; cerebral perfusion; cerebrovascular reserve; cerebral hyperperfusion syndrome; RNF213; precision cerebrovascular surgery.
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