Ebata Yuho, Fukuda Yutaka, Nakamura Hikaru, Chikamatsu Genki, Shiozaki Eri, Moritsuka Tomoya, Hiu Takeshi, Kawahara Ichiro, Ono Tomonori, Haraguchi Wataru, Ushijima Ryujiro, Tsutsumi Keisuke
Residency Program, Department of Neurosurgery, National Hospital Organization Nagasaki Medical Center.
No Shinkei Geka. 2019 Oct;47(10):1073-1079. doi: 10.11477/mf.1436204076.
We report a rare case of reversible cerebral vasoconstriction syndrome(RCVS)with cortical subarachnoid hemorrhage(cSAH)associated with a fresh cortical infarction beneath the sulcus with thick cSAH. A 34-year-old woman presented with history of thunderclap headache. She was transferred to our hospital for further examination of a cSAH in the left frontal lobe. Results of the cerebrospinal fluid examination were unremarkable, but three-dimensional rotational angiography revealed multiple instances of narrowing of the cortical branches of the anterior and middle cerebral arteries, suggesting the diagnosis of RCVS. Diffusion weighted imaging(DWI)demonstrated a small cortical area with high-signal intensity around the sulcus , where a thick cSAH clot was observed. This cortical lesion appeared as low-signal intensity on the apparent diffusion coefficient maps, and the follow-up T2-weighted images(obtained 3 months after onset)demonstrated a residual lesion that was smaller than the initial DWI abnormality with high-signal intensity;thus indicating the presence of a coincident fresh cortical infarction. The position of the infarct next to the thickest portion of cSAH suggested that it was the bleeding source of the cSAH. Ten days after onset, the cerebral blood flow and volume in the cortex around the cSAH increased as compared to the same area on the contralateral side. These findings suggested that at least one of the bleeding mechanisms of the cSAH was related to the hemorrhagic infarction or subpial hemorrhage resulting from the "ischemia-reperfusion injury" due to the acute disturbance of the pial vessel microcirculation with subsequent rapid resolution of the blood flow during the early phases of RCVS. These dynamics could not be demonstrated with contemporary angiographic imaging.
我们报告了一例罕见的可逆性脑血管收缩综合征(RCVS),伴有皮质下蛛网膜下腔出血(cSAH),且在伴有厚层cSAH的脑沟下方存在新鲜的皮质梗死。一名34岁女性因霹雳样头痛就诊。她被转诊至我院进一步检查左额叶的cSAH。脑脊液检查结果无异常,但 但三维旋转血管造影显示大脑前动脉和大脑中动脉皮质分支多处狭窄,提示诊断为RCVS。扩散加权成像(DWI)显示脑沟周围一个小的皮质区域呈高信号强度,在该处观察到厚层cSAH血凝块。该皮质病变在表观扩散系数图上呈低信号强度,随访T2加权图像(发病3个月后获得)显示残留病变小于初始DWI上的高信号异常,从而表明存在同时发生的新鲜皮质梗死。梗死灶位于cSAH最厚部分旁边的位置提示它是cSAH的出血来源。发病10天后,与对侧同一区域相比,cSAH周围皮质的脑血流量和血容量增加。这些发现表明,cSAH的出血机制中至少有一个与软脑膜血管微循环急性紊乱导致的“缺血再灌注损伤”引起的出血性梗死或软脑膜下出血有关,随后在RCVS早期血流迅速恢复。这些动态变化无法通过当代血管造影成像显示。