Degenerative Thoracic Myelopathy: A Scoping Review of Epidemiology, Genetics, and Pathogenesis

Author:

Rujeedawa Tanzil1ORCID,Mowforth Oliver D.1ORCID,Davies Benjamin M.1ORCID,Yang Cylene1,Nouri Aria12ORCID,Francis Jibin J.1,Aarabi Bizhan3,Kwon Brian K.4,Harrop James5,Wilson Jefferson R.6ORCID,Martin Allan R.7,Rahimi-Movaghar Vafa8,Guest James D.9,Fehlings Michael G.10ORCID,Kotter Mark R.1

Affiliation:

1. Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK

2. Department of Clinical Neurosciences, Geneva University Hospitals, Geneva, Switzerland

3. University of Maryland, Baltimore, MD, USA

4. Vancouver General Hospital, University of British Columbia, Vancouver, BC, Canada

5. Thomas Jefferson University Hospital, Philadelphia, PA, USA

6. University of Toronto, Toronto, ON, Canada

7. Department of Neurosurgery, University of California Davis, Sacramento, CA, USA

8. Department of Neurosurgery, Sina Trauma and Surgery Research Center, Tehran University of Medical Sciences, Tehran, Iran

9. Department of Neurosurgery and The Miami Project to Cure Paralysis, The Miller School of Medicine, University of Miami, Miami, FL, USA

10. Toronto Western Hospital, University Health Network, University of Toronto, Toronto, ON, Canada

Abstract

Study Design Literature Review. Objective Myelopathy affecting the thoracic spinal cord can arise secondary to several aetiologies which have similar presentation and management. Consequently, there are many uncertainties in this area, including optimal terminology and definitions. Recent collaborative cervical spinal research has led to the proposal and subsequent community adoption of the name degenerative cervical myelopathy(DCM), which has facilitated the establishment of internationally-agreed research priorities for DCM. We put forward the case for the introduction of the term degenerative thoracic myelopathy(DTM) and degenerative spinal myelopathy(DSM) as an umbrella term for both DCM and DTM. Methods Following PRISMA guidelines, a systematic literature search was performed to identify degenerative thoracic myelopathy literature in Embase and MEDLINE. Results Conditions encompassed within DTM include thoracic spondylotic myelopathy, ossification of the posterior longitudinal ligament, ossification of the ligamentum flavum, calcification of ligaments, hypertrophy of ligaments, degenerative disc disease, thoracic osteoarthritis, intervertebral disc herniation, and posterior osteophytosis. The classic presentation includes girdle pain, gait disturbance, leg weakness, sensory disturbance, and bladder or bowel dysfunction, often with associated back pain. Surgical management is typically favoured with post-surgical outcomes dependent on many factors, including the causative pathology, and presence of additional stenosis. Conclusion The clinical entities encompassed by the term DTM are interrelated, can manifest concurrently, and present similarly. Building on the consensus adoption of DCM in the cervical spine and the recent proposal of degenerative cervical radiculopathy(DCR), extending this common nomenclature framework to the terms degenerative spinal myelopathy and degenerative thoracic myelopathy will help improve recognition and communication.

Funder

University of Cambridge

Publisher

SAGE Publications

Subject

Neurology (clinical),Orthopedics and Sports Medicine,Surgery

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