单侧烟雾病所致急性硬膜下血肿合并皮质下出血后脑动脉血管合并颅成形术治疗。

IF 0.9 Q4 CLINICAL NEUROLOGY
Naoki Kato, Shota Kakizaki, Yusuke Hirokawa, Shotaro Michishita, Takuya Ishii, Tohru Terao, Yuichi Murayama
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引用次数: 0

摘要

烟雾病常在成年患者颅内出血后诊断。在此,我们报告一例单侧烟雾病,在急性硬膜下血肿和皮质下出血治疗后,采用间接血运重建术联合颅骨成形术治疗。一位意识紊乱的中年妇女被转送到我院。计算机断层扫描显示急性硬膜下血肿伴左颞顶叶皮质下出血。三维CT血管造影显示左侧大脑中动脉(MCA)几乎没有增强,怀疑由于颅内压升高而延迟或不充盈。随后行血肿引流和体外减压。术后数字减影血管造影(DSA)显示左MCA及烟雾血管狭窄,提示单侧烟雾病。初次手术后45天,我们使用颞浅动脉进行脑动脉合并术(EAS),同时颅骨成形术治疗颅骨缺损。患者出院后1年修正Rankin量表评分为1分,重复DSA显示EAS通畅良好。对于出血性烟雾病,如果患者在减压开颅术后颅骨缺损需要颅骨成形术,第二步使用EAS进行血运重建可作为血运重建的一种选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Encephalo-Arterio-Synangiosis with Cranioplasty after Treatment of Acute Subdural Hematoma Associated with Subcortical Hemorrhage Due to Unilateral Moyamoya Disease.

Encephalo-Arterio-Synangiosis with Cranioplasty after Treatment of Acute Subdural Hematoma Associated with Subcortical Hemorrhage Due to Unilateral Moyamoya Disease.

Encephalo-Arterio-Synangiosis with Cranioplasty after Treatment of Acute Subdural Hematoma Associated with Subcortical Hemorrhage Due to Unilateral Moyamoya Disease.

Encephalo-Arterio-Synangiosis with Cranioplasty after Treatment of Acute Subdural Hematoma Associated with Subcortical Hemorrhage Due to Unilateral Moyamoya Disease.

Moyamoya disease is often diagnosed after intracranial hemorrhage in adult patients. Here, we report a case of unilateral moyamoya disease treated with indirect revascularization combined with cranioplasty after treatment for acute subdural hematoma and subcortical hemorrhage. A middle-aged woman with disturbed consciousness was transferred to our hospital. Computed tomography (CT) revealed an acute subdural hematoma with left temporoparietal subcortical hemorrhage. Three-dimensional CT angiography indicated a scarcely enhanced left middle cerebral artery (MCA) that was suspected to be delayed or nonfilling due to increased intracranial pressure. Subsequently, hematoma evacuation and external decompression were performed. Postoperative digital subtraction angiography (DSA) revealed stenosis of the left MCA and moyamoya vessels, indicating unilateral moyamoya disease. Forty-five days after the initial procedure, we performed encephalo-arterio-synangiosis (EAS) using the superficial temporal artery simultaneously with cranioplasty for the skull defect. The modified Rankin Scale score of the patient one year after discharge was 1, and the repeat DSA showed good patency of the EAS. Revascularization using EAS in the second step can be an option for revascularization for hemorrhagic moyamoya disease if the patient required cranioplasty for postoperative skull defect after decompressive craniotomy.

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