From the Department of Radiology (M.B., L.G.M., L.M.v.d.G., M.A.v.B., S.v.R., L.v.d.W.).
Department of Human Genetics (M.B., L.G.M., L.M.v.d.G., L.v.d.W.).
Stroke. 2018 Sep;49(9):2081-2087. doi: 10.1161/STROKEAHA.118.021872.
Background and Purpose- Previous studies of symptomatic and asymptomatic hereditary cerebral amyloid angiopathy (CAA) patients offered the possibility to study the radiological manifestations of CAA in the early stages of the disease. Recently, a striped cortex, observable as hypointense lines perpendicular to the pial surface on T-weighted 7T magnetic resonance imaging (MRI), was detected in 40% of the symptomatic hereditary CAA patients. However, the origin of these MRI contrast changes is unknown. This study aimed at defining the underlying pathology associated with the in vivo observed striped pattern. Methods- Formalin-fixed postmortem brain material including the occipital lobe of 4 hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D) cases and 6 sporadic CAA cases were selected from local neuropathology tissue collections. Depending on the availability of the material, intact hemispheres or brain slabs including the occipital lobe of these patients were screened for the presence of a striped cortex. Regions containing the striped cortex were then subjected to high-resolution 7T MRI and histopathologic examination. Results- We found 2 hereditary cerebral hemorrhage with amyloidosis-Dutch type cases and 1 sporadic CAA case with striped patterns in the occipital cortex resembling the in vivo signal. Histopathologic examination showed that the striped pattern in the cortex at 7T MRI is because of iron accumulation and calcification of penetrating arteries. The presence of both nonheme iron and calcification on penetrating arteries causes signal loss and hence the abnormal striped patterns in the cortical ribbon on T-weighted MRI. Conclusions- We identified iron accumulation and calcification of the vessel wall in hereditary cerebral hemorrhage with amyloidosis-Dutch type as the histopathologic correlates of the striped cortex observed on in vivo 7T MRI.
背景与目的- 先前对有症状和无症状遗传性脑淀粉样血管病(CAA)患者的研究提供了研究 CAA 在疾病早期放射学表现的可能性。最近,在 40%的有症状遗传性 CAA 患者中,在 T 加权 7T 磁共振成像(MRI)上观察到垂直于脑皮层表面的条纹状皮层,表现为低信号线。然而,这些 MRI 对比变化的起源尚不清楚。本研究旨在确定与体内观察到的条纹模式相关的潜在病理学。方法- 从当地神经病理学组织库中选择了 4 例遗传性脑出血伴淀粉样变性-荷兰型(HCHWA-D)病例和 6 例散发性 CAA 病例的福尔马林固定的尸检脑组织材料,包括枕叶。根据材料的可用性,筛选这些患者的完整大脑半球或包括枕叶的脑片是否存在条纹皮层。然后,将包含条纹皮层的区域进行高分辨率 7T MRI 和组织病理学检查。结果- 我们发现 2 例遗传性脑出血伴淀粉样变性-荷兰型和 1 例散发性 CAA 病例的枕叶皮层存在类似体内信号的条纹模式。组织病理学检查显示,7T MRI 皮层中的条纹模式是由于穿透性动脉的铁积累和钙化所致。穿透性动脉中非血红素铁和钙化的存在导致信号丢失,从而导致 T 加权 MRI 上皮质带的异常条纹模式。结论- 我们确定遗传性脑出血伴淀粉样变性-荷兰型的血管壁铁积累和钙化是体内 7T MRI 观察到条纹皮层的组织病理学相关性。