Retained medullary cord extending to a sacral subcutaneous meningocele

Childs Nerv Syst. 2018 Mar;34(3):527-533. doi: 10.1007/s00381-017-3644-2. Epub 2017 Nov 3.

Abstract

Background: A retained medullary cord (RMC) is a rare closed spinal dysraphism with a robust elongated neural structure continuous from the conus and extending to the dural cul-de-sac. One case extending down to the base of a subcutaneous meningocele at the sacral level has been reported.

Clinical presentation: We report on three cases of closed spinal dysraphism, in which a spinal cord-like tethering structure extended out from the dural cul-de-sac and terminated at a skin-covered meningocele sac in the sacrococcygeal region, which was well delineated in curvilinear coronal reconstructed images of 3D-heavily T2-weighted images (3D-hT2WI). Intraoperative neurophysiology revealed the spinal cord-like tethering structure was nonfunctional, and histopathology showed that it consisted of central nervous system tissue, consistent with RMC. The tethering structure histologically contained a glioneuronal core with an ependymal-like lumen and smooth muscle, which may indicate developmental failure during secondary neurulation.

Conclusions: When the RMC extending to a meningocele is demonstrated with the detailed magnet resonance imaging including 3D-hT2WI, decision to cut the cord-like structure for untethering of the nervous tissue should be made under careful intraoperative neurophysiological monitoring.

Keywords: Mesoderm; Myelomeningocele; Secondary neurulation; Smooth muscle; Tethered cord.

Publication types

  • Case Reports

MeSH terms

  • Female
  • Humans
  • Imaging, Three-Dimensional / methods
  • Infant
  • Infant, Newborn
  • Male
  • Meningocele / diagnostic imaging
  • Meningocele / surgery*
  • Neural Tube Defects / diagnostic imaging
  • Neural Tube Defects / surgery*
  • Sacrum / diagnostic imaging
  • Sacrum / surgery*
  • Spinal Dysraphism / diagnostic imaging
  • Spinal Dysraphism / surgery*