Type I split cord malformation and tethered cord syndrome in an adult patient: A case report and literature review

Author:

D’Agostino Erin N.1,Calnan Daniel R.2,Makler Vyacheslav I.3,Khan Imad2,Kanter John H.2,Bauer David F.2

Affiliation:

1. Department of Neurosurgery, Geisel School of Medicine, Dartmouth College, Hanover, United States.

2. Dartmouth-Hitchcock Medical Center, Section of Neurosurgery, 1 Medical Center Drive, Lebanon, New Hampshire, United States.

3. Section of Neurology, 1 Medical Center Drive, Lebanon, New Hampshire, United States.

Abstract

Background: In a split cord malformation (SCM), the spinal cord is divided longitudinally into two distinct hemicords that later rejoin. This can result in a tethered cord syndrome (TCS). Rarely, TCS secondary to SCM presents in adulthood. Here, we present an adult female with Type I SCM resulting in TCS and a review of literature. Case Description: A 57-year-old female with a history of spina bifida occulta presented with a 2-year history of worsening back and left leg pain, difficulty with ambulation, and intermittent urinary incontinence; she had not responded to conservative therapy. Magnetic resonance imaging (MRI) revealed a tethered cord secondary to lumbar type I SCM. The patient underwent an L1–S1 laminectomy for resection of the bony septum with cord detethering. At 2-month follow-up, the patient had improvement in her motor symptoms and less pain. In literature, 25 cases of adult-onset surgically managed SCM with TCS were identified (between 1936 and 2018). Patients averaged 37 years of age at the time of diagnosis, and 56% were female. Conclusion: TCS can present secondary to SCM in adulthood and is characterized predominantly by back and leg pain.

Publisher

Scientific Scholar

Subject

Neurology (clinical),Surgery

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