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[脑血管多发异常。1例伴大脑中动脉开窗及持续性原始三叉动脉的多发动脉瘤]

[Multiple anomalies of cerebral vessels. A case of multiple aneurysms associated with fenestration of the middle cerebral artery and persistent primitive trigeminal artery].

作者信息

Ueda T, Goya T, Kinoshita K, Wakuta Y, Mihara K

出版信息

No Shinkei Geka. 1984 Mar;12(4):531-6.

PMID:6738800
Abstract

A case of multiple intracranial anomalies was reported. They consisted of fenestration of the middle cerebral artery (MCA), persistent primitive trigeminal artery and four intracranial aneurysms. The patient, 45-year-old male, had an attack of subarachnoid hemorrhage on July 15, 1982. He was transferred and admitted to our Dept. of Neurosurgery on July 27. On admission neurological examinations revealed retinal hemorrhage, bilateral papilledema and abducens nerve paresis on the left. Cerebral angiography demonstrated multiple aneurysms, one in the left vertebral artery, one in the left MCA, one in the right IC-PC junction and one in the fenestrated right MCA and persistent primitive trigeminal artery. Computed tomography (CT) demonstrated high density areas in the basal cistern and bilateral sylvian fissures, and cavum septi pellucidi and cavum Vergae as well. Surgical intervention was done and all aneurysms were clipped or coated successfully. The aneurysm in the fenestrated right MCA had originated from the proximal end of the fenestration of the MCA. The cavum septi pellucidi and cavum Vergae were asymptomatic. The postoperative course was uneventful. The authors discussed the pathogenesis and clinical meanings of fenestration of the MCA and persistent primitive trigeminal artery, and inferred that the genetic abnormality at the stage of development of cerebral vessels could play one part of the formation of intracranial aneurysms, because of the fact that the cerebrovascular anomalies showed high incidence of coexistence of intracranial aneurysms.

摘要

报告了一例颅内多发性异常病例。这些异常包括大脑中动脉(MCA)开窗、永存原始三叉动脉和四个颅内动脉瘤。患者为45岁男性,于1982年7月15日发生蛛网膜下腔出血。7月27日转至并入住我院神经外科。入院时神经检查发现视网膜出血、双侧视乳头水肿和左侧展神经麻痹。脑血管造影显示多发性动脉瘤,一个位于左侧椎动脉,一个位于左侧大脑中动脉,一个位于右侧颈内动脉-后交通动脉交界处,一个位于右侧大脑中动脉开窗处及永存原始三叉动脉。计算机断层扫描(CT)显示基底池和双侧外侧裂有高密度区,以及透明隔腔和韦尔加腔。进行了手术干预,所有动脉瘤均成功夹闭或包裹。右侧大脑中动脉开窗处的动脉瘤起源于大脑中动脉开窗的近端。透明隔腔和韦尔加腔无症状。术后病程平稳。作者讨论了大脑中动脉开窗和永存原始三叉动脉的发病机制及临床意义,并推断脑血管发育阶段的基因异常可能在颅内动脉瘤形成中起一定作用,因为脑血管异常显示颅内动脉瘤共存的发生率较高。

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