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48 - Myelopathies

from PART V - DISORDERS OF SPINE AND SPINAL CORD

Published online by Cambridge University Press:  05 August 2016

Philip D. Thompson
Affiliation:
University Department of Medicine, University of Adelaide and Department of Neurology, Royal Adelaide Hospital
Peter C. Blumbergs
Affiliation:
Department of Neuropathology, Institute of Medical and Veterinary Science and University Department of Medicine, University of Adelaide, South Australia
Arthur K. Asbury
Affiliation:
University of Pennsylvania School of Medicine
Guy M. McKhann
Affiliation:
The Johns Hopkins University School of Medicine
W. Ian McDonald
Affiliation:
University College London
Peter J. Goadsby
Affiliation:
University College London
Justin C. McArthur
Affiliation:
The Johns Hopkins University School of Medicine
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Summary

An etiological classification of myelopathies yields an extensive list of diverse conditions (Table 48.1). In clinical practice, myelopathies are classified into spinal cord syndromes, based on patterns of neurological symptoms and signs, which identify the anatomical location and distribution of spinal cord pathology. The time course of symptoms is useful in distinguishing between different etiologies. Vascular lesions generally present with acute onset or rapid progression of symptoms. Inflammatory disease evolves in a subacute manner and may fluctuate over days or weeks. Compressive lesions also may present with a subacute onset and generally have a progressive course. Degenerative myelopathies are usually slowly progressive over months or years. The evolution and type of spinal cord syndrome suggest certain diagnostic possibilities and guide appropriate investigation.

Symptoms and signs of spinal cord disease

Motor symptoms and signs

The clinical presentation of an evolving myelopathy often is precipitated by limb weakness and spasticity due to corticospinal tract involvement. Arm and leg weakness suggests a cervical cord lesion. A paraparesis, with leg weakness or walking difficulty alone, suggests a lesion of the thoracic spinal cord or below. Progressive cervical cord lesions may evolve in a sequence, beginning with weakness of the arm ipsilateral to the lesion, followed by weakness of the ipsilateral then contralateral leg, and finally the contralateral arm.

Exacerbation of symptoms by exercise, or during increases in body temperature (hot weather or a hot bath) suggests demyelination, but may also occur in dural arteriovenous malformations of the spinal cord.

Motor signs of spinal cord disease reflect involvement of the long tracts of the spinal cord with increased muscle tone, brisk tendon reflexes, extensor plantar responses and weakness of hip and knee flexion and ankle dorsiflexion. Involvement of the anterior horn cells or anterior (motor) spinal nerve roots produces additional lower motor neuron signs of segmental wasting and weakness (Table 48.2).

Sensory symptoms and signs

Back pain

Back pain is often an early complaint of a myelopathy, preceding any motor symptoms. The site of pain may localize the level of a focal structural lesion such as a spinal epidural abscess, vertebral body collapse or intervertebral disc prolapse. Dull, poorly localized backache is common in intrinsic spinal lesions but is of little localizing or diagnostic value.

Type
Chapter
Information
Diseases of the Nervous System
Clinical Neuroscience and Therapeutic Principles
, pp. 713 - 726
Publisher: Cambridge University Press
Print publication year: 2002

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  • Myelopathies
    • By Philip D. Thompson, University Department of Medicine, University of Adelaide and Department of Neurology, Royal Adelaide Hospital, Peter C. Blumbergs, Department of Neuropathology, Institute of Medical and Veterinary Science and University Department of Medicine, University of Adelaide, South Australia
  • Edited by Arthur K. Asbury, University of Pennsylvania School of Medicine, Guy M. McKhann, The Johns Hopkins University School of Medicine, W. Ian McDonald, University College London, Peter J. Goadsby, University College London, Justin C. McArthur, The Johns Hopkins University School of Medicine
  • Book: Diseases of the Nervous System
  • Online publication: 05 August 2016
  • Chapter DOI: https://doi.org/10.1017/CBO9781316134993.049
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  • Myelopathies
    • By Philip D. Thompson, University Department of Medicine, University of Adelaide and Department of Neurology, Royal Adelaide Hospital, Peter C. Blumbergs, Department of Neuropathology, Institute of Medical and Veterinary Science and University Department of Medicine, University of Adelaide, South Australia
  • Edited by Arthur K. Asbury, University of Pennsylvania School of Medicine, Guy M. McKhann, The Johns Hopkins University School of Medicine, W. Ian McDonald, University College London, Peter J. Goadsby, University College London, Justin C. McArthur, The Johns Hopkins University School of Medicine
  • Book: Diseases of the Nervous System
  • Online publication: 05 August 2016
  • Chapter DOI: https://doi.org/10.1017/CBO9781316134993.049
Available formats
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Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

  • Myelopathies
    • By Philip D. Thompson, University Department of Medicine, University of Adelaide and Department of Neurology, Royal Adelaide Hospital, Peter C. Blumbergs, Department of Neuropathology, Institute of Medical and Veterinary Science and University Department of Medicine, University of Adelaide, South Australia
  • Edited by Arthur K. Asbury, University of Pennsylvania School of Medicine, Guy M. McKhann, The Johns Hopkins University School of Medicine, W. Ian McDonald, University College London, Peter J. Goadsby, University College London, Justin C. McArthur, The Johns Hopkins University School of Medicine
  • Book: Diseases of the Nervous System
  • Online publication: 05 August 2016
  • Chapter DOI: https://doi.org/10.1017/CBO9781316134993.049
Available formats
×