Literature DB >> 26588497

Thoracolumbar kyphoscoliosis with unilateral subluxation of the spine and postoperative lumbar spondylolisthesis in Hunter syndrome.

Simon B Roberts1, Athanasios I Tsirikos1.   

Abstract

Surgical correction for kyphoscoliosis is increasingly being performed for patients with mucopolysaccharidosis (MPS). Reported case series have predominantly included patients with Type I (Hurler) and Type IV (Morquio) MPS. To their knowledge, the authors describe the first case report of surgical management of thoracolumbar kyphoscoliosis in Hunter syndrome (MPS Type II) and the rare occurrence of lumbar spondylolisthesis following surgical stabilization. A 12-year-old boy with Hunter syndrome presented with severe thoracolumbar kyphoscoliosis and no associated symptoms. Spinal radiographs demonstrated kyphosis of 48° (T11-L3) and scoliosis of 22° (T11-L3) with an anteriorly hypoplastic L-1 vertebra. The deformity progressed to kyphosis of 60° and scoliosis of 42° prior to surgical intervention. Spinal CT scans identified left T12-L1 facet subluxation, causing anterior rotatory displacement of the spine proximal to L-1 and bilateral L-5 isthmic spondylolysis with no spondylolisthesis. A combined single-stage anterior and posterior instrumented spinal arthrodesis from T-9 to L-4 was performed. Kyphosis and scoliosis were corrected to 4° and 0°, respectively. Prolonged ventilator support and nasogastric feedings were required for 3 months postoperatively. At 2.5 years following surgery, the patient was asymptomatic, mobilizing independently, and had achieved a solid spinal fusion. However, he had also developed a Grade II spondylolisthesis at L4-5; this was managed nonoperatively in the absence of symptoms or further deterioration of the spondylolisthesis to the 3.5-year postoperative follow-up visit. Satisfactory correction of thoracolumbar kyphoscoliosis in Hunter syndrome can be achieved by combined anterior/posterior instrumented arthrodesis. The risk of developing deformity or instability in motion segments adjacent to an instrumented fusion may be greater in patients with MPS related to the underlying connective tissue disorder.

Entities:  

Keywords:  Hunter syndrome; MPS = mucopolysaccharidosis; deformity; kyphoscoliosis; mucopolysaccharidosis; spondylolisthesis; thoracolumbar

Mesh:

Year:  2015        PMID: 26588497     DOI: 10.3171/2015.6.SPINE15268

Source DB:  PubMed          Journal:  J Neurosurg Spine        ISSN: 1547-5646


  4 in total

1.  Incidence of spinal deformity surgery in a national health service from 2005 to 2018: an analysis of 2,205 children and adolescents.

Authors:  Athanasios I Tsirikos; Simon B Roberts; Emma Bhatti
Journal:  Bone Jt Open       Date:  2020-10-27

2.  Adolescent idiopathic scoliosis associated POC5 mutation impairs cell cycle, cilia length and centrosome protein interactions.

Authors:  Amani Hassan; Stefan Parent; Hélène Mathieu; Charlotte Zaouter; Sirinart Molidperee; Edward T Bagu; Soraya Barchi; Isabelle Villemure; Shunmoogum A Patten; Florina Moldovan
Journal:  PLoS One       Date:  2019-03-07       Impact factor: 3.240

3.  Adjunct diagnostic value of radiological findings in mucopolysaccharidosis type IVa-related thoracic spinal abnormalities: a pilot study.

Authors:  Ya-Ting Jan; Pei-Shan Tsai; Wen-Hui Huang; Shih-Chieh Huang; Yu-Peng Liu; She-Meng Cheng; Kun-Shuo Huang
Journal:  Orphanet J Rare Dis       Date:  2022-07-29       Impact factor: 4.303

4.  Does orthopaedic surgery improve quality of life and function in patients with mucopolysaccharidoses?

Authors:  N Williams; D Challoumas; D M Eastwood
Journal:  J Child Orthop       Date:  2017-08-01       Impact factor: 1.548

  4 in total

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