Yokota A, Matsukado Y
Childs Brain. 1979;5(4):380-97.
5 cases of dysgenetic hydrocephaly associated with scalp anomalies are described. This brain-scalp anomaly complex is characterized by congenital hydrocephalus, alopecia or cephalocele in the parietal midline and symmetrical defect of the bilateral posterior cerebral mantle along the midline. Midline septal structures of the cranial cavity and tentorium cerebelli were also defective and replaced by a huge dorsal CSF cavity. Histological features of the covering membrane of the dorsal cyst indicate that this new brain anomaly is the consequence of a porencephalic process and we postulate the 'midline porencephaly'. Cerebral angiography is the most valuable method for the diagnosis of this anomaly and its venous phase reveals dysgenesis of the galenic drainage as well as of the dural sinuses.
本文描述了5例伴有头皮异常的发育不全性脑积水病例。这种脑-头皮异常复合体的特征是先天性脑积水、顶叶中线处的脱发或脑膨出以及沿中线的双侧大脑后叶对称缺损。颅腔和小脑幕的中线间隔结构也有缺陷,并被一个巨大的背侧脑脊液腔所取代。背侧囊肿覆盖膜的组织学特征表明,这种新的脑异常是脑穿通畸形过程的结果,我们推测为“中线脑穿通畸形”。脑血管造影是诊断这种异常最有价值的方法,其静脉期显示大脑大静脉引流以及硬脑膜窦发育不全。