Sporadic cerebral amyloid angiopathy (CAA) is a common neurodegenerative disorder characterized by accumulation of amyloid β (Aβ) in the cerebrovascular wall, often coexisting with Alzheimer’s disease. CAA is thought to be caused by impaired efflux of Aβ through small vessels. However, the precise locations of Aβ accumulation within the spatial cerebrovascular system remain unclear in the human brain because of its large size and complex organization. This study aimed to clarify the three-dimensional (3D) distribution and possible progression pattern of Aβ and vascular degeneration in relation to perivascular senile plaques in CAA, employing a highly tissue-clearing technique and light-sheet fluorescence microscopy. We prepared formalin-fixed 0.5-cm3 tissue blocks from the frontal and occipital lobes of postmortem brains of six patients with CAA (CAA Thal stage 2 or 3 and Braak stage III-VI) using double-immunofluorescence labeling for smooth muscle actin (SMA) and Aβ17-24. We identified 1104 Aβ-positive and 535 Aβ-negative vascular units. The 3D analysis revealed that Aβ deposition was predominantly distributed in the leptomeningeal arteries (LMA) and superficial cortical segment within Aβ-positive vascular units (96.2% and 99.5% positivity, respectively), and appeared to develop continuously from the brain surface to deeper vascular segments. Similar to this pattern, SMA loss was common in leptomeningeal and cortical surface segments within Aβ-positive vascular units, and these units had a significantly larger median external diameter than those that were Aβ-negative (36.73 μm vs 25.94 μm, P<0.0001). The density of perivascular plaques was significantly lower around Aβ-positive than around Aβ-negative vascular units (P<0.0001). These findings suggest that Aβ deposition in CAA develops preferentially from the cerebral surface and extends to the deeper layer. There may be an inverse relationship between the perivascular and vascular Aβ loads.