Neuroblastoma in a Patient With Spinal Muscular Atrophy Type I: Is It Just a Coincidence?

J Child Neurol. 2015 Jul;30(8):1075-8. doi: 10.1177/0883073814542950. Epub 2014 Aug 14.

Abstract

Spinal muscular atrophy is an autosomal recessive disorder characterized by progressive degeneration of anterior horn cells of the spinal cord resulting in hypotonia, skeletal muscle atrophy, and weakness. Herein, we report a 4-month-old male infant who presented to our hospital with an abdominal mass that was diagnosed as neuroblastoma and spinal muscular atrophy type I. We would like to discuss the course and differential diagnosis with an algorithm leading to the diagnosis in this peculiar patient. To our knowledge, coexistence of spinal muscular atrophy type I and neuroblastoma is defined for the first time in the literature.

Keywords: abdominal mass; muscle weakness; neuroblastoma; spinal muscular atrophy type I.

Publication types

  • Case Reports

MeSH terms

  • Brain Neoplasms / complications*
  • Humans
  • Infant
  • Male
  • Mutation / genetics
  • Neuroblastoma / complications*
  • Spinal Muscular Atrophies of Childhood / complications*
  • Spinal Muscular Atrophies of Childhood / genetics
  • Survival of Motor Neuron 1 Protein / genetics

Substances

  • SMN1 protein, human
  • Survival of Motor Neuron 1 Protein