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[一例反复发生皮质下血肿且初始血管造影正常的脑动静脉畸形病例]

[A case of cerebral arteriovenous malformation revealed at repeated subcortical hematoma with initially normal angiogram].

作者信息

Isayama Y, Nakagawara J, Takeda R, Wada K, Hyogo T, Sasaki T, Nakamura J, Suematsu K

机构信息

Department of Neurosurgery, Nakamura Memorial Hospital, Sapporo, Japan.

出版信息

No Shinkei Geka. 1991 Dec;19(12):1175-80.

PMID:1766544
Abstract

An 18-year-old male admitted to our hospital suffered left temporal subcortical hemorrhage. No abnormality was demonstrated on carotid or vertebral angiography at that time. On the day following the onset, left frontotemporal craniotomy was performed and the subcortical hematoma was evacuated. No vascular malformation was found despite careful investigation. On 30th day after the onset, the repeat cerebral angiography was performed but failed to show any vascular abnormalities. After discharge he was in good health, and had had some follow up, CT were normal except for the hematoma cavity. Just two years after the first operation he suffered a second left temporal hemorrhage. Cerebral angiography was repeated and a temporal arteriovenous malformation (AVM) was found with feeding vessels from the M-1 and M-2 portion of the left middle cerebral artery and from the left anterior choroidal artery, and draining veins to vein of Rosenthal and the straight sinus. One month after the second hemorrhage, left frontotemporal craniotomy was performed and complete excision of the AVM was carried out. Only five cases of AVMs in patients with normal angiograms several years before have been reported previously in the literature. But there are no cases in which surgery has been performed. Differently to those cases, in this case it was investigated operatively whether there was a vascular abnormality at the first hemorrhage. We didn't think, however, that the AVM demonstrated at the second hemorrhage had developed spontaneously because there had been a hemorrhage of unknown origin previous to it. It was assumed that a small angiographically occult AVM connected to the hematoma cavity existed at the time of the first hemorrhage but it was too small to be found even during surgical procedure. Such an angiography occult AVM had been growing for two years, and its growth had probably been facilitated by the presence of the hematoma cavity left after the first operation.

摘要

一名18岁男性入住我院,发生左侧颞叶皮质下出血。当时颈动脉或椎动脉血管造影未显示异常。发病次日,行左额颞开颅术,清除皮质下血肿。尽管仔细检查,未发现血管畸形。发病后第30天,再次进行脑血管造影,但未显示任何血管异常。出院后他健康状况良好,接受了一些随访,除血肿腔外,CT检查均正常。首次手术后仅两年,他再次发生左侧颞叶出血。再次进行脑血管造影,发现一个颞叶动静脉畸形(AVM),供血血管来自左大脑中动脉M-1和M-2段以及左脉络膜前动脉,引流静脉汇入Rosenthal静脉和直窦。第二次出血后一个月,行左额颞开颅术,完整切除AVM。此前文献中仅报道过几例数年前血管造影正常的患者发生AVM的病例。但尚无手术治疗的病例。与那些病例不同的是,本例在首次出血时对是否存在血管异常进行了手术探查。然而,我们认为第二次出血时发现的AVM并非自发形成,因为在此之前曾发生过一次不明原因的出血。推测首次出血时存在一个与血肿腔相连的血管造影隐匿性小AVM,但即使在手术过程中也太小而无法发现。这样一个血管造影隐匿性AVM已经生长了两年,其生长可能因首次手术后留下的血肿腔而加速。

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