Coordinated approach to spinal and tracheal reconstruction in a patient with morquio syndrome

Int J Pediatr Otorhinolaryngol. 2020 Jan:128:109721. doi: 10.1016/j.ijporl.2019.109721. Epub 2019 Oct 11.

Abstract

Morquio syndrome (Mucopolysaccharidosis IVA) is an autosomal recessive lysosomal storage disease with manifestations ranging from mild to severe phenotype. Mechanical spinal cord injury and airway insufficiency are major causes of mortality. A 17-year-old male patient with severe Morquio syndrome presented with cervical and upper thoracic spinal stenosis with spinal cord myelopathy, and progressive severe tracheal stenosis. Coordinated care among otolaryngology, orthopedic surgery, neurosurgery, anesthesiology, cardiovascular surgery, radiology, and pulmonology teams facilitated the successful planning and execution of two major surgical interventions in rapid succession. This is the first description of a successful coordinated spine and airway repair in the literature.

Keywords: Airway modeling; Airway stenosis/reconstruction; Mucopolysaccharidosis; Multidisciplinary; Pediatric airway; Tracheal stenosis.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Humans
  • Male
  • Models, Anatomic
  • Mucopolysaccharidosis IV / surgery*
  • Otorhinolaryngologic Surgical Procedures / methods*
  • Patient Care Team / organization & administration*
  • Printing, Three-Dimensional
  • Spinal Cord Diseases / surgery
  • Spinal Stenosis / surgery*
  • Surgery, Computer-Assisted
  • Thoracic Vertebrae / surgery
  • Tracheal Stenosis / surgery*