Giant arteriovenous aneurysm of the posterior fossa in a three-month-old infant.

Child's brain Pub Date : 1983-01-01 DOI:10.1159/000120105
E Schijman, J A Monges
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引用次数: 8

Abstract

A 3-month-old female infant presented a 20-day history of drowsiness and maturing deterioration. The neurological exam showed peripheric facial palsy on the right side and a brachiocrural hemiparesis on the left. A brain scan revealed a lesion of avascular content in the posterior fossa. The computed tomography scan showed hydrocephalus and a high-density lesion, nonenhanced after introduction of the contrast agent, compatible with a clot at posterior fossa level. Likewise, after contrast new images appeared which had not been seen previously, considered as afferent and efferent vascular elements to the lesion. The cerebral angiography showed an avascular lesion in the cerebellar vermis with important hypertrophy of arterial and venous elements, although no steal phenomena of neighbouring areas was evident. These findings, and the absence of cardiac failure, suggested the diagnosis, confirmed by surgery, of giant clotted arteriovenous malformation. The patient has done well postoperatively.

3个月大婴儿后颅窝巨大动静脉动脉瘤。
一个3个月大的女婴表现出20天的嗜睡和成熟恶化史。神经学检查显示右侧周围性面瘫和左侧臂丛农村偏瘫。脑部扫描显示后颅窝无血管内容物病变。计算机断层扫描显示脑积水和高密度病变,引入造影剂后无增强,与后窝水平的血块相容。同样,对比后出现以前未见的新图像,被认为是病变的传入和传出血管元素。脑血管造影显示小脑蚓部有一血管性病变,动脉和静脉元素明显肥大,但邻近区域未见明显的偷窃现象。这些发现,并没有心衰,提示诊断,经手术证实,巨大凝血动静脉畸形。病人术后情况良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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