Embryonic hydromyelia: cystic dilatation of the lumbosacral neural tube in human embryos

Acta Neuropathol. 2002 Mar;103(3):248-54. doi: 10.1007/s00401-001-0465-9. Epub 2001 Dec 21.

Abstract

In a large collection of human embryos (the Kyoto Collection of Human Embryos, Kyoto University), we encountered five cases with abnormal dilatation of the neural tube at the lumbosacral level. In these examples, the central canal was enlarged, and the roof plate of the neural tube was extremely thin and expanded. The mesenchymal tissue was scarce or lacking between the roof plate and the surface ectoderm. This type of anomaly was assumed to be formed after neural tube closure and may be an early form of spina bifida. In two of the cases, some abnormal cells were found ectopically between the thin roof plate and the surface ectoderm. Morphologically, these cells resembled those forming spinal ganglia and could be of the neural crest origin. Since neural crest cells are pluripotent and can differentiate into a variety of tissues, such ectopic cells might undergo abnormal differentiation into teratomatous tumors and/or lipomas, which are frequently associated with spina bifida. We also discuss the definition of spina bifida and the classification of neural tube defects from the embryological and pathogenic viewpoints and propose a new classification of neural tube defects.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Dilatation, Pathologic / embryology
  • Dilatation, Pathologic / genetics
  • Dilatation, Pathologic / pathology
  • Humans
  • Lumbosacral Region / abnormalities*
  • Lumbosacral Region / embryology*
  • Lumbosacral Region / pathology
  • Neural Tube Defects / embryology*
  • Neural Tube Defects / genetics
  • Neural Tube Defects / pathology
  • Spinal Cord / embryology
  • Spinal Cord / pathology
  • Spinal Dysraphism / embryology*
  • Spinal Dysraphism / genetics
  • Spinal Dysraphism / pathology