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An Extremely Rare Association of Posterior Fossa Arachnoid Cyst with Chiari I Malformation and Syringomyelia in a Child: A Short Report

机译:与Chiari I畸形和儿童倾角畸形和辛疹术的极少数罕见的稀有关联:一份简短的报告

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摘要

Arachnoid cysts are benign, congenital, intra-arachnoid lesions. Posterior fossa arachnoid cyst associated with Chiari I malformation and syringomyelia is rare with none reported in children [1-3, 5-9]. Authors report the first of such an association in a 5-year-old child. A 5-year-old boy presented with suboc-cipital headache, neck pain and mild gait disturbance of 6 months’ duration. Neurological examination was unremarkable. He had undergone ventroperitoneal shunting 2 years previously at the referring hospital. MRI revealed a supracerebellar arachnoid cyst with severe tonsillar herniation up to the C_3 level and C_7-T_(10) level syringomyelia. Ventricles were adequately decompressed, and there was no communication of the cyst with the fourth ventricle (fig. la-c). Dynamic radiographs of the craniovertebral junction ruled out any bony instability.
机译:蛛网膜囊肿是良性的,先天性,蛛网膜内的病变。 与Chiari I的后窝蛛网囊肿囊肿畸形和杨氏炎症是罕见的,没有报告的儿童[1-3,5-9]。 作者在一个5岁的孩子中报道了第一个协议。 一个5岁的男孩介绍了Suboc Cipital头痛,颈部疼痛和轻度步态障碍6个月的持续时间。 神经学检查是不起眼的。 他在参考医院之前经过了2年的腹包内分流。 MRI揭示了一只具有严重的扁桃体突出的颅内骨肉囊肿,直至C_3水平和C_7-T_(10)水平射点。 心室被充分减压,并且没有与第四心室的囊肿的通信(图la-c)。 Craniovertebral结的动态射线照片排除了任何骨不稳定性。

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