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[三例以壳核出血为表现的基底节区隐匿性动静脉畸形]

[Three cases of cryptic arteriovenous malformation in basal ganglia manifested by putaminal hemorrhage].

作者信息

Niwa J, Okuyama T, Kubota T, Shimizu K, Hirai H

机构信息

Department of Neurosurgery, Hakodate Municipal Hospital.

出版信息

No Shinkei Geka. 1990 Jul;18(7):665-8.

PMID:2203992
Abstract

Three cases of histologically proven cryptic arteriovenous (AV) malformation of the basal ganglia are reported. Seventeen cases of patients showing putaminal hemorrhage in the CT scan underwent craniotomy for evacuation of a hematoma between January 1986 and December 1988. The preoperative diagnosis was hypertensive putaminal hemorrhage. In all three cases a network of abnormal vessels around the internal capsule was detected at surgery. Case 1: A 62-year-old male was admitted to our hospital with consciousness disturbance (JCS 20), total aphasia and right hemiparesis. The CT scan showed left putaminal hemorrhage. The volume of the hematoma was 45 ml by CT criteria. Left carotid angiography did not demonstrate any abnormal findings. Case 2: 69-year-old male was admitted with consciousness disturbance (JCS 10) and right hemiparesis. Left putaminal hemorrhage (volume 25 ml) was recognized on the CT scan. Two hours after admission, the consciousness level suddenly deteriorated (JCS 100). At that moment, the volume of the putaminal hematoma had increased to 100 ml. AV malformation was not detected by left carotid angiography. Case 3: A 50-year-old male was admitted with consciousness disturbance (JCS 20), total aphasia and right hemiparesis. The CT scan showed left putaminal hemorrhage of 73 ml. Pathohistological examination proved AV malformation in each case. The three cases described here suggest the following; 1) The incidence of the basal ganglia cryptic AV malformation has been considered low, but meticulous examination shows that among the cases diagnosed as hypertensive hemorrhage, AV malformation is not infrequently the hidden cause.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

报告了3例经组织学证实的基底节隐匿性动静脉畸形。1986年1月至1988年12月期间,17例CT扫描显示壳核出血的患者接受了开颅血肿清除术。术前诊断为高血压性壳核出血。在所有3例手术中均发现内囊周围有异常血管网。病例1:一名62岁男性因意识障碍(日本昏迷评分20分)、完全性失语和右侧偏瘫入院。CT扫描显示左侧壳核出血。根据CT标准,血肿体积为45毫升。左侧颈动脉血管造影未显示任何异常发现。病例2:一名69岁男性因意识障碍(日本昏迷评分10分)和右侧偏瘫入院。CT扫描显示左侧壳核出血(体积25毫升)。入院2小时后,意识水平突然恶化(日本昏迷评分100分)。此时,壳核血肿体积已增至100毫升。左侧颈动脉血管造影未发现动静脉畸形。病例3:一名50岁男性因意识障碍(日本昏迷评分20分)、完全性失语和右侧偏瘫入院。CT扫描显示左侧壳核出血73毫升。病理组织学检查证实每例均为动静脉畸形。这里描述的3例病例提示如下:1)基底节隐匿性动静脉畸形的发病率一直被认为较低,但仔细检查发现,在诊断为高血压性出血的病例中,动静脉畸形往往是隐藏的病因。(摘要截断于250字)

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