Literature DB >> 32673810

Rare Presentation: A Report of 2 Identical Cases with Thoracic Compressive Myelopathy in Down Syndrome.

Himanshu Champaneri1, Anirban Deep Banerjee2.   

Abstract

BACKGROUND: Atlantoaxial instability, a common finding in patients with Down syndrome (DS), is attributed to laxity of ligamentous structures. Cervical spondylosis identified in these patients has a pathogenesis of ligament laxity and early degeneration compared with the normal population. No cases have been reported showing affection of thoracic or lower levels. CASE DESCRIPTION: Two adults with DS presented with progressive spastic paraparesis with hypertrophy of ligamentum flavum at the lower thoracic level, causing canal stenosis and myelopathy. Degenerative changes were seen in the entire spine. Both patients improved with canal decompression.
CONCLUSIONS: Degenerative changes of the spine occur earlier in DS, probably due to increased movements across the vertebrae owing to laxity in the ligaments. Routine workup of patients with DS presenting in their adult lives should keep in mind the affection of lower spinal levels. Early identification of thoracic myelopathy and lumbar canal stenosis gives a chance of cure.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Degenerative spine disease; Down syndrome; Thoracic compressive myelopathy

Mesh:

Year:  2020        PMID: 32673810     DOI: 10.1016/j.wneu.2020.07.040

Source DB:  PubMed          Journal:  World Neurosurg        ISSN: 1878-8750            Impact factor:   2.104


  1 in total

1.  Hirayama-like disease in the thoracic spine.

Authors:  Maria Braileanu; Michael Hoch; Sandra Rincon; Brent Weinberg
Journal:  Radiol Case Rep       Date:  2021-03-20
  1 in total

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