Growing Skull Defect in an Infant with a Rare Combination of a Foramen Parietale Permagna and an Atretic Cephalocele

M. Ratliff, A. Unterberg, H. Bächli
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Abstract

Here we present a case of a 2-month-old child with an atretic encephalocele and large persistent parietal foramina. The course was unusual in that the parietal foramina significantly increased in size over a relatively short time. At the age of three months the child required surgery because of the increasing skull defect. During surgery the cause of the growing skull defect was revealed as a medial atretic encephalocele with enlarged parietal foramina. Large parietal foramina are a rare clinical entity with a prevalence ranging from 1:15.000 to 1:25.000. The skull defect is usually identified on physical examination and confirmed radio graphically. We assume that the mechanism underlying the growing bone defect is identical to that of a growing skull fracture. To our knowledge this is the only reported case of an infant with a growing skull defect requiring surgery due to an atretic encephalocele protruding through a growing parietal foramina. 
婴儿颅骨缺损伴罕见的顶骨大孔合并闭锁性头膨出
在这里我们提出一个2个月大的孩子闭锁脑膨出和大持久顶骨孔。这个过程是不寻常的,因为顶骨孔的大小在相对较短的时间内显著增加。在三个月大的时候,由于颅骨缺损的增加,孩子需要手术。手术中发现颅骨缺损的原因为内侧闭锁性脑膨出伴顶骨孔扩大。大顶骨孔是一种罕见的临床疾病,患病率为1:15.000至1:25.000。颅骨缺损通常在体格检查中发现并经影像学证实。我们假设生长的骨缺损的机制与生长的颅骨骨折相同。据我们所知,这是唯一一例由于闭锁脑膨出通过生长的顶骨孔而导致婴儿颅骨缺损需要手术治疗的病例。
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