Yamada H, Sakata K, Kashiki Y, Okuma A, Takada M
Childs Brain. 1979;5(4):426-32. doi: 10.1159/000119838.
3 infantile cases of congenital parieto-occipital midline soft tumor, the clinical and pathological findings of which did not correspond precisely to a known congenital head tumor, are reported. One of them probably belongs to McLaurin's type of encephalocele with heterotopic glial rest, and the remaining two to McLaurin's type of meningocele without central connection. The types of anomaly shown by the present cases should generally be called 'atretic cephalocele' or 'rudimentary cephalocele'.
报告了3例先天性顶枕部中线软组织肿瘤的婴儿病例，其临床和病理表现与已知的先天性头部肿瘤并不完全相符。其中1例可能属于伴有异位神经胶质细胞残余的麦克劳林型脑膨出，其余2例属于无中央连接的麦克劳林型脑膜膨出。本病例所显示的异常类型一般应称为“闭锁性脑膨出”或“发育不全性脑膨出”。
