Journal of Craniovertebral Junction and Spine

CASE REPORT
Year
: 2017  |  Volume : 8  |  Issue : 3  |  Page : 288--290

Idiopathic thoracic transdural intravertebral spinal cord herniation


Mazda K Turel, Joshua T Wewel, Mena G Kerolus, John E O'Toole 
 Department of Neurosurgery, Rush University Medical Center, Chicago, IL, USA

Correspondence Address:
Mazda K Turel
Department of Neurosurgery, Rush University Medical Center, 1725 W Harrison Street, Suite 855, Chicago, IL
USA

Abstract

Idiopathic spinal cord herniation is a rare and often missed cause of thoracic myelopathy. The clinical presentation and radiological appearance is inconsistent and commonly confused with a dorsal arachnoid cyst and often is a misdiagnosed entity. While ventral spinal cord herniation through a dural defect has been previously described, intravertebral herniation is a distinct entity and extremely rare. We present the case of a 70-year old man with idiopathic thoracic transdural intravertebral spinal cord herniation and discuss the clinico-radiological presentation, pathophysiology and operative management along with a review the literature of this unusual entity.



How to cite this article:
Turel MK, Wewel JT, Kerolus MG, O'Toole JE. Idiopathic thoracic transdural intravertebral spinal cord herniation.J Craniovert Jun Spine 2017;8:288-290


How to cite this URL:
Turel MK, Wewel JT, Kerolus MG, O'Toole JE. Idiopathic thoracic transdural intravertebral spinal cord herniation. J Craniovert Jun Spine [serial online] 2017 [cited 2022 Jul 5 ];8:288-290
Available from: https://www.jcvjs.com/text.asp?2017/8/3/288/215203


Full Text

 Introduction



Idiopathic spinal cord herniation is an uncommon cause of thoracic myelopathy. The presentation can vary from back pain to spastic paraparesis with bowel and bladder dysfunction. The clinical presentation and radiological appearance are inconsistent and commonly confused with a dorsal arachnoid cyst and often is a misdiagnosed entity.[1] While several cases of idiopathic spinal cord herniation have been described in the literature, to the best of our knowledge, only three previous reports specify idiopathic transvertebral herniation.[2],[3],[4] With this report, we add to the existing knowledge of this rare pathology.

 Case Report



We present the case of a 70-year-old male patient with 1-year history of ataxia and several months history of new urinary urgency and occasional incontinence. On physical examination, he had 5/5 strength, normal sensation, and subtle spasticity with exaggerated lower limbs reflexes.

Magnetic resonance imaging revealed a T6 ventral cord herniation through a dural defect with enlargement of the dorsal thoracic subarachnoid space [Figure 1]a and [Figure 1]b. There was a significant erosion of the posterior vertebral body of T6. A cerebrospinal fluid (CSF) cleft was present between the spinal cord and the vertebral body. Computed tomography myelogram confirmed the diagnosis and ruled out an arachnoid cyst. It clearly demonstrated the bony defect within the dorsal vertebral body [Figure 1]c and [Figure 1]d.{Figure 1}

Due to the patient's progressive symptoms, surgery was offered, and the patient underwent a T6 laminectomy, intradural exploration and repair of the ventral spinal cord herniation. Intraoperative ultrasound was used after the laminectomy to examine the intradural contents and confirm adequate exposure to address the spinal cord herniation. A midline durotomy was performed, and with gentle elevation of the dentate ligament, the ventral spinal cord was visible. The herniated portion of the spinal cord was evident emanating through a dural defect, and the vertebral bony erosion seen on pre-operative imaging was visualized [Figure 2]a and [Figure 2]b. A small piece of a dural substitute (Durepair, Medtronic, Minneapolis, MN, USA) was then cut into an appropriate size and carefully placed into the ventral intradural space, to cover the dural defect [Figure 2]c and [Figure 2]d. The dorsal durotomy was then closed using a running 5-0 Gore-Tex suture (Gore Medical, Flagstaff, AZ, USA). The wound was closed in layers. He was ambulatory on postoperative day 1 and was discharged on postoperative day 2. At follow-up, he had substantial improvement of his preoperative symptoms with normalization of urinary function and steady gait.{Figure 2}

 Discussion



Most cases of idiopathic spinal cord herniation occur either anteriorly or anterolaterally between T2 and T8.[1] While the diagnosis of idiopathic ventral spinal cord herniation is a challenging one, involvement of the vertebral body can confound the diagnosis even further. The CSF cleft ventral to the cord causing erosion of the posterior cortical margin can occasionally be mistaken for a bony cyst.[4] If diagnosis is delayed the focal area of transdural migration can cause incarceration of the cord and result in paraplegia.[3] Barbagallo et al.[2] suggested that in this subset of patients with vertebral body involvement, the presentation is more atypical, the outcome unpredictable and probably worse than in more typical cases.

The etiology of this entity remains unclear and is thought to be due to either a congenital dural defect or an acquired defect secondary to erosion of the dura from a thoracic disc. While direct trauma can result in a pseudomyelomeningocele eroding into the vertebral body, its occurrence in an idiopathic fashion is rare.[5] Najjar et al.[6] hypothesized that herniation occurs as an acquired phenomenon due to an inflammatory process resulting in adherence between the spinal cord and the dura. Continued erosion of the vertebral body occurs due to CSF pulsations and a dural defect forms. This is followed by herniation of the spinal cord into the vertebral body occurring with CSF pulsations.

Surgical strategies have evolved over time in the treatment of ventral spinal cord herniations. Closure of the dura has been attempted by either primarily suturing the dura or by layering the defect with various artificial dural patches. Some authors have described simply widening the dural defect to prevent strangulation of the cord.[6] We prefer to simply place a piece of artificial dural replacement intradurally over the dural defect that is fashioned to a size just larger than the defect. This “patch” acts like a sling preventing the spinal cord from re-herniating through the defect. We have not seen any recurrences using this technique in the past 10 years. While we did not see any reason to address the bony defect, Sadek et al.[4] describe packing it with bone wax amalgamated with vancomycin powder.

Transvertebral spinal cord herniation is a rare entity and distinct from the typical ventral spinal cord herniation. Accurate diagnosis and work-up are essential for appropriate surgical planning. Along with the presented clinical case and radiographic imaging, our intraoperative photos provide a resource for surgeons to visualize what is to be expected intraoperatively.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

References

1Darbar A, Krishnamurthy S, Holsapple JW, Hodge CJ Jr. Ventral thoracic spinal cord herniation: Frequently misdiagnosed entity. Spine (Phila Pa 1976). 2006;31:E600-5.
2Barbagallo GM, Marshman LA, Hardwidge C, Gullan RW. Thoracic idiopathic spinal cord herniation at the vertebral body level: A subgroup with a poor prognosis? Case reports and review of the literature. J Neurosurg 2002;97 3 Suppl: 369-74.
3Wortzman G, Tasker RR, Rewcastle NB, Richardson JC, Pearson FG. Spontaneous incarcerated herniation of the spinal cord into a vertebral body: A unique cause of paraplegia. Case report. J Neurosurg 1974;41:631-5.
4Sadek AR, Nader-Sepahi A. Idiopathic thoracic intravertebral spinal cord herniation. Br J Neurosurg 2016:1-2. [Epub ahead of print].
5Sachdev VP, Huang YP, Shah CP, Malis LI. Posttraumatic pseudomeningomyelocele (enlarging fracture?) in a vertebral body. Case report. J Neurosurg 1981;54:545-9.
6Najjar MW, Baeesa SS, Lingawi SS. Idiopathic spinal cord herniation: A new theory of pathogenesis. Surg Neurol 2004;62:161-70.