Yang Chin-An, Peng Steven Shinn-Forng, Hsieh Wu-Shiun, Tsao Po-Nien, Chen Chien-Yi, Chou Hung-Chieh
Department of Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, No. 8, Chung San South Road, Taipei, Taiwan.
Department of Medical Imaging, National Taiwan University Hospital, Taipei, Taiwan.
Childs Nerv Syst. 2013 Jul;29(7):1069-72. doi: 10.1007/s00381-013-2096-6. Epub 2013 Apr 5.
Midline cranial defects can be divided into lesions with intracranial tissue herniation (cranium bifidum cysticum) and lesions mainly with ossification failure (cranium bifidum occultum). Herniated cephaloceles mostly require surgical resection, while persisted parietal foramina might become smaller with age.
Here, we report a neonate with large symmetric midline skull defect at high parietal area. A mild bulging mass was noticed. Interestingly, unlike sac herniation, it was surrounded by bony ridges extended from the rim of the calvarial defect, which suggests aberrant ossification. Persistent falcine sinus was also detected. At the corrected age of 11 months, the size of the skull defect had decreased spontaneously, favoring the diagnosis of parietal bone ossification defect. Potential mechanisms resulting in the special appearance of skull bone were discussed.
Incomplete closing of the parietal foramina might be expected due to the aberrant ridge formation. We suggest protective measures for the calvarial defect.
颅中线缺损可分为伴有颅内组织疝出的病变(囊性颅裂)和主要因骨化失败引起的病变(隐性颅裂)。疝出的脑膨出大多需要手术切除,而持续存在的顶骨孔可能会随着年龄增长而变小。
在此,我们报告一名新生儿,其顶叶高位区域存在巨大对称性颅中线颅骨缺损。发现有一个轻度隆起的肿块。有趣的是,与囊状疝不同,它被从颅骨缺损边缘延伸的骨嵴所包围,这提示骨化异常。还检测到持续存在的大脑镰窦。在矫正年龄11个月时,颅骨缺损大小已自发减小,支持顶骨骨化缺损的诊断。讨论了导致颅骨特殊外观的潜在机制。
由于异常嵴的形成,可能会出现顶骨孔闭合不全。我们建议对颅骨缺损采取保护措施。