Longitudinally extensive myelopathy in children

Danielle Eckart Sorte1, Andrea Poretti, Scott D Newsome

  • 1Division of Interventional Neuroradiology, The Russell H. Morgan Department of Radiology and Radiological Science, School of Medicine, Johns Hopkins University, Baltimore, MD, USA.

Pediatric Radiology
|February 1, 2015
PubMed

Insights

Pediatric acute myelopathy requires MRI of the neuraxis. This study reviews differential diagnoses for longitudinally extensive spinal cord signal abnormalities in children, excluding trauma.

Area of Science:

  • Pediatric Neurology
  • Neuroradiology
  • Spinal Cord Imaging

Background:

  • Acute myelopathy in children presents with sensory, motor, or bowel/bladder dysfunction.
  • Magnetic Resonance Imaging (MRI) of the neuraxis with contrast is crucial for diagnosis.
  • Longitudinally extensive transverse myelitis is classically associated with Neuromyelitis Optica (NMO), but other causes exist.

Purpose of the Study:

  • To review differential diagnoses for longitudinally extensive spinal cord signal abnormalities in pediatric patients.
  • To highlight the role of radiologists in identifying diverse etiologies of myelopathy in children.

Main Methods:

  • Pictorial essay format reviewing imaging findings.
  • Focus on MRI demonstrating signal abnormalities within the spinal cord.
  • Discussion of various etiological categories presenting as myelopathy.

Main Results:

  • MRI frequently shows spinal cord signal abnormalities in pediatric acute myelopathy.
  • Longitudinally extensive abnormalities can stem from multiple causes beyond NMO.
  • Differential diagnoses include inflammatory, infectious, vascular, metabolic, and neurodegenerative conditions.

Conclusions:

  • Radiologists must be aware of the broad spectrum of diseases causing longitudinally extensive spinal cord signal abnormalities in children.
  • Accurate diagnosis aids in appropriate management of pediatric myelopathy.
  • Distinguishing these findings from trauma-related injuries is essential.

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