Altered sensory-motor plasticity in amyotrophic lateral sclerosis and complex regional pain type I syndrome: a shared mechanism?

Neurol Sci. 2020 Jul;41(7):1919-1921. doi: 10.1007/s10072-020-04317-5. Epub 2020 Mar 5.

Abstract

Besides the prominent motor syndrome, some patients affected by amyotrophic lateral sclerosis (ALS) complain of many non-motor symptoms during the disease course, in particular chronic pain that significantly reduces the patients' quality of life. Complex regional pain syndrome (CRPS) is a rare painful condition, rarely described in ALS patients. We present the clinical case of a patient affected by spinal-onset ALS, who developed a type I CRPS (CRPS-I) at the upper limbs. To the best of our knowledge, only five cases of ALS-CRPS-I have been reported and they share some peculiar features: ALS spinal-onset with classic phenotype, rapid deterioration of quality of life, and a poor prognosis. Different mechanisms have been supposed in the pathogenesis of both CRPS and ALS, resulting in distinctive clinical presentations. Altered plasticity of brain sensory and motor areas might represent a common feature that seems to influence negatively ALS progression and prognosis.

Keywords: Altered plasticity; Amyotrophic lateral sclerosis; Chronic pain; Complex regional pain syndrome.

Publication types

  • Case Reports

MeSH terms

  • Amyotrophic Lateral Sclerosis* / complications
  • Humans
  • Motor Cortex*
  • Pain
  • Quality of Life
  • Reflex Sympathetic Dystrophy*