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Updated: Apr 7, 2026

Experimental Strategies to Bridge Large Tissue Gaps in the Injured Spinal Cord after Acute and Chronic Lesion
Published on: April 5, 2016
Spinal cord detethering in children with tethered cord syndrome and Chiari type 1 malformations
Chad Glenn1, Ahmed A Cheema1, Sam Safavi-Abbasi1
1Department of Neurosurgery, University of Oklahoma Health Sciences Center, Suite 400, 1000 North Lincoln Boulevard, Oklahoma City, OK 73104, USA.
Insights
Sectioning the filum terminale improved symptoms in children with tethered cord syndrome (TCS) and Chiari type 1 malformation (CM1). Surgical outcomes were positive, with no worsening of neurological function observed post-operation.
Area of Science:
- Neurosurgery
- Pediatric Neurology
- Spinal Cord Disorders
Background:
- The association between tethered cord syndrome (TCS) and Chiari type 1 malformation (CM1) remains unclear.
- TCS involves the spinal cord being abnormally attached to surrounding tissue, restricting movement.
- CM1 is a condition where brain tissue extends into the spinal canal.
Purpose of the Study:
- To investigate the surgical outcomes of children with coexisting CM1 and TCS who underwent filum terminale sectioning (SFT).
- To analyze the relationship between filum terminale characteristics and tonsillar herniation in this patient group.
Main Methods:
- Retrospective review of 170 spinal cord detethering surgeries performed between 2008 and 2012.
- Identification and analysis of 17 pediatric patients with both CM1 and TCS who underwent SFT.
- Evaluation of clinical presentation, radiographic findings, surgical procedures, and post-operative outcomes.
Main Results:
- A mean tonsillar herniation of 10.0mm was observed in patients with CM1 and TCS.
- Fatty or thickened filum terminale correlated with greater tonsillar displacement (p<0.005).
- All 17 children experienced improvement in preoperative symptoms following SFT, with no neurological decline.
Conclusions:
- Filum terminale sectioning is an effective treatment for pediatric patients with CM1 and TCS, even those without classic Chiari symptoms.
- SFT can lead to symptomatic improvement in this specific patient population.
- Post-operative MRI showed stable tonsillar position in most patients, indicating the safety and efficacy of the procedure.
Abstract:
We discuss the association between tethered cord syndrome (TCS) and Chiari type 1 malformation (CM1), and report on the surgical outcomes of children with CM1 and TCS who underwent sectioning of the filum terminale (SFT). The relationship between TCS and CM1 is unclear. A retrospective review of 170 consecutive spinal cord detetherings between 2008 and 2012 was performed. We identified 17 children with CM1 who underwent SFT. Information regarding clinical presentation, radiographic findings, surgical procedures, and clinical outcomes was analyzed. A mean tonsillar herniation of 10.0mm (range: 5-21) was noted. Children with a fatty or thickened filum terminale demonstrated a greater amount of tonsillar displacement (p<0.005). A low conus medullaris was found in 12 children and a syrinx was present in three. The preoperative symptoms improved in all children. The postoperative MRI (mean 21.8 months) revealed an unchanged tonsillar position in all but one child. No worsening of neurologic function was noted. Pediatric patients who have both CM1 and TCS, but do not demonstrate classic Chiari-related symptoms, may experience symptomatic improvement after filum terminale sectioning.
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