TY - JOUR
T1 - Retained medullary cord extending to a sacral subcutaneous meningocele
AU - Murakami, Nobuya
AU - Morioka, Takato
AU - Shimogawa, Takafumi
AU - Hashiguchi, Kimiaki
AU - Mukae, Nobutaka
AU - Uchihashi, Kazuyoshi
AU - Suzuki, Satoshi O.
AU - Iihara, Koji
N1 - Funding Information:
Acknowledgments We thank Ann Turnley, PhD, from Edanz Group (www.edanzediting.com/ac) for editing a draft of this manuscript. This work was partly supported by Research Foundation of Fukuoka Children’s Hospital.
Publisher Copyright:
© 2017, Springer-Verlag GmbH Germany.
PY - 2018/3/1
Y1 - 2018/3/1
N2 - 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.
AB - 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.
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U2 - 10.1007/s00381-017-3644-2
DO - 10.1007/s00381-017-3644-2
M3 - Article
C2 - 29101613
AN - SCOPUS:85032838710
SN - 0256-7040
VL - 34
SP - 527
EP - 533
JO - Child's Nervous System
JF - Child's Nervous System
IS - 3
ER -