Neonatal intraoperative neuromonitoring in thoracic myelocystocele: a case report.
Tracy M FlandersAlier J FrancoScott J HinesJesse A TaylorGregory G HeuerPublished in: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery (2019)
Thoracic myelocystocele are extremely rare, non-terminal, closed neural tube defects. Intraoperative neuromonitoring (IONM) is a mainstay of pediatric spinal surgery. However, in neonates and infants, incomplete myelination of the corticospinal tract presents unique challenges to successful use of IONM in this vulnerable patient population. Surgery can often be delayed until patients are older, but there are circumstances in which early intervention is necessary. We report a case of T6 myelocystocele resection and wound closure in an infant on day of life 15 with the use of IONM. To our knowledge, this is the youngest reported patient to undergo successful IONM in the spinal cord. Given that the majority of thoracic myelocystoceles present without any neurological deficits, early intervention for this rare closed spinal dysraphism is sometimes necessary. This case study reports the possibility of IONM use in neonatal patients and also highlights the techniques that make its use more possible.
Keyphrases
- spinal cord
- end stage renal disease
- randomized controlled trial
- ejection fraction
- newly diagnosed
- minimally invasive
- chronic kidney disease
- prognostic factors
- spinal cord injury
- neuropathic pain
- physical activity
- patients undergoing
- emergency department
- surgical site infection
- young adults
- coronary artery disease
- brain injury
- patient reported outcomes
- atrial fibrillation
- preterm infants
- patient reported
- middle aged
- community dwelling