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首页> 外文期刊>Journal of Clinical and Diagnostic Research >Dandy-Walker Malformation with an Occipital Cephalocele in an Infant: A Case Report
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Dandy-Walker Malformation with an Occipital Cephalocele in an Infant: A Case Report

机译：Dandy-Walker畸形与婴儿的枕骨Cockalocele：案例报告

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Dandy-Walker Malformation (DWM) is an unusual hereditary intracranial anomaly that affects the cerebellum and its componentsand is also characterised with an enlarged posterior fossa. DWM can appear dramatically or develop unnoticed and occurs withoccipital cephalocele in about 5% of cases. This is a case report of a 10-month-old male child with DWM who had a co-existingoccipital cephalocele and presented on account of hydrocephalus and poor developmental milestone. He had a Contrast EnhancedComputed Tomographic (CECT) scan of the brain; which showed a posterior fossa cysts, a hypoplastic cerebellar vermis with adysmorphic fourth ventricle that appear continuous with the posterior fossa cyst giving the so called ‘key hole deformity’. There isalso associated hydrocephalus with an occipital cephalocele.
机译：Dandy-Walker畸形（DWM）是一种不寻常的遗传性颅内异常，影响小脑，其成分也具有扩大的后窝。 DWM可以急剧显现或未被忽视，并且在约5％的情况下用麻油头皮细胞发生。这是一个10个月大的男孩的案例报告，DWM患有共同现有的Cephalocele，并根据脑积水和差的发育里程碑呈现。他对大脑进行了对比增强的仿胀断层（CECT）扫描;显示出后窝囊肿，一种具有伴态第四脑室的软骨细菌蚓，与后部窝囊肿显得连续，使得所谓的“关键孔畸形”。有肌肉相关的脑膜肿伴有枕骨Cocele。

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