Osaka K, Matsumoto S, Tanimura T
Childs Brain. 1978;4(6):347-59. doi: 10.1159/000119791.
Four early human embryos with open myeloschisis are reported. These are a thoracolumbar myeloschisis in Carnegie developmental stage 12, a cervical myeloschisis in stage 13, and two lumbosacral myeloschisis in stage 14. All of them are the smallest human embryos with this type of malformation ever reported. In these embryos, the neuroectodermal junction is smooth and there is no microscopic evidence that the neural tube is forced open after its proper closure. The presence of the lesion in such early embryos, especially in one of stage 12, implies that the lesion evolved from the neural plate which never closed. Cellular polarity and the limiting membrane in the lesion are generally well preserved in spite of apparent overgrowth of the neural tissue. These findings do not support the hypothesis of LEMIRE et al. that the defective external limiting membrane predisposes to a loss of cellular polarity and resultant neural overgrowth.
报道了4例开放性脊柱裂的早期人类胚胎。其中1例为卡内基发育阶段12期的胸腰段脊柱裂,1例为13期的颈段脊柱裂,2例为14期的腰骶段脊柱裂。所有这些都是有此类畸形报道的最小的人类胚胎。在这些胚胎中,神经外胚层交界处光滑,没有微观证据表明神经管在正常闭合后被迫开放。这种早期胚胎中病变的存在,尤其是在12期的一个胚胎中,意味着病变是从从未闭合的神经板演变而来的。尽管神经组织明显过度生长,但病变中的细胞极性和限制膜通常保存良好。这些发现不支持勒米尔等人的假说,即有缺陷的外部限制膜易导致细胞极性丧失和由此产生的神经组织过度生长。